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Ca2+-dependent redox modulation of SERCA 2b by ERp57
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     Department of Physiology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229

    Address correspondence to Patricia Camacho, Dept. of Physiology, MSC 7756, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78229-3900. Tel.: (210) 567-6558. Fax: (210) 567–4410. email: camacho@uthscsa.edu

    Abstract

    We demonstrated previously that calreticulin (CRT) interacts with the lumenal COOH-terminal sequence of sarco endoplasmic reticulum (ER) calcium ATPase (SERCA) 2b to inhibit Ca2+ oscillations. Work from other laboratories demonstrated that CRT also interacts with the ER oxidoreductase, ER protein 57 (also known as ER-60, GRP58; ERp57) during folding of nascent glycoproteins. In this paper, we demonstrate that ERp57 overexpression reduces the frequency of Ca2+ oscillations enhanced by SERCA 2b. In contrast, overexpression of SERCA 2b mutants defective in cysteines located in intralumenal loop 4 (L4) increase Ca2+ oscillation frequency. In vitro, we demonstrate a Ca2+-dependent and -specific interaction between ERp57 and L4. Interestingly, ERp57 does not affect the activity of SERCA 2a or SERCA 2b mutants lacking the CRT binding site. Overexpression of CRT domains that disrupt the interaction of CRT with ERp57 behave as dominant negatives in the Ca2+ oscillation assay. Our results suggest that ERp57 modulates the redox state of ER facing thiols in SERCA 2b in a Ca2+-dependent manner, providing dynamic control of ER Ca2+ homeostasis.

    Key Words: calreticulin; calcium ATPases; endoplasmic reticulum; calcium oscillations; glycoprotein folding

    Abbreviations used in this paper: ER, ER Ca2+ concentration; CLNX, calnexin; CRT, calreticulin; ERp57, ER protein 57 (also known as ER-60, GRP58); IP3R, inositol 1,4,5-trisphosphate receptor; L4, loop 4; PDI, protein disulfide isomerase; SERCA, sarco ER calcium ATPase; t1/2, decay time.

    Introduction

    Changes in the cytosolic Ca2+ concentration control many essential cellular responses (Dolmetsch et al., 1997; Berridge et al., 1998; Li et al., 1998; Hajnoczky et al., 2003). To coordinate these functions Ca2+ signals are flexible, yet precisely regulated. At intermediate IP3 concentrations (i.e., 300 nM), cytosolic Ca2+ oscillates in Xenopus oocytes (Camacho and Lechleiter, 1993, 1995; John et al., 1998; Roderick et al., 2000; Falcke et al., 2003). Ca2+ oscillations are triggered by opening of the inositol 1,4,5-trisphosphate receptor (IP3R) channel, whereas reuptake of the cation into the ER lumen is due to the activity of the sarco ER calcium ATPases (SERCAs). Consistent with this model, overexpression of SERCA pumps increases IP3 induced Ca2+ oscillations (Camacho and Lechleiter, 1993). SERCA pumps play a critical role not only in clearing cytosolic Ca2+, but also in maintaining ER Ca2+ concentrations (ER). At rest, the free ER is 300 μM, whereas cytosolic Ca2+ concentration is three to four orders of magnitude lower (5–50 nM; Pozzan et al., 1994).

    The lumen of the ER is a specialized protein-folding environment. It contains molecular chaperones such as calreticulin (CRT), calnexin (CLNX), and ER protein 57 (also known as ER-60, GRP58; ERp57; High et al., 2000; Ellgaard and Helenius, 2003; Kostova and Wolf, 2003; Schrag et al., 2003). Optimal ER is necessary for protein folding (Ashby and Tepikin, 2001). ER Ca2+ depletion inhibits protein folding and maturation (Hardman and Wetmore, 1996; Chen et al., 1997) and facilitates protein degradation (Ramsden et al., 2000). Ca2+ can also regulate the formation of chaperone complexes in the ER (Corbett et al., 1999).

    ERp57 is a ubiquitous ER thiol-dependent oxidoreductase that promotes the formation of intra- or intermolecular disulfide bonds during glycoprotein folding (Marcus et al., 1996; High et al., 2000; Ellgaard and Helenius, 2003; Kostova and Wolf, 2003; Schrag et al., 2003). ERp57 has also been identified as a key component in the assembly of class I major histocompatibility complexes (Hughes and Cresswell, 1998; Lindquist et al., 1998; Morrice and Powis, 1998; Antoniou et al., 2002; Dick et al., 2002; Bouvier, 2003). Critical to our paper is the demonstration, firmly established in the literature, of a specific interaction between either CLNX or CRT with ERp57 (Oliver et al., 1997, 1999; Van der Wal et al., 1998; Zapun et al., 1998; High et al., 2000; Frickel et al., 2002).

    Our group discovered that CRT, as well as CLNX, inhibited Ca2+ oscillations using the Xenopus oocyte system (Camacho and Lechleiter, 1995; John et al., 1998; Roderick et al., 2000). The precise molecular mechanism responsible for this inhibitory effect is not completely known, however, CRT and CLNX may directly regulate SERCA 2b or they may recruit other enzymes such as ERp57 to cause the effect. Two conserved cysteines in the longest ER facing loop 4 (L4) of SERCA 2b are potential targets of ERp57. In this paper, we address the issues of whether ERp57 modulates Ca2+ oscillations through an interaction with L4 thiols; whether this interaction requires the enzymatic activity of ERp57; whether the interaction is specific and Ca2+ dependent; and whether CRT is required to recruit ERp57 to L4.

    Results

    Coexpression ERp57 with SERCA 2b reduces the frequency of Ca2+ oscillations

    We used a confocal Ca2+ oscillation assay as a tool to investigate the modulation of the SERCA 2b pump activity. In this assay, increases in Ca2+ oscillation frequency (shorter period between oscillations and/or decay time of individual waves) reflect increased Ca2+ ATPase activity and vice versa (Camacho and Lechleiter, 1993, 1995, 2000; John et al., 1998; Roderick et al., 2000; Falcke et al., 2003). To test whether ERp57 modulates SERCA 2b activity in Xenopus oocytes, we coexpressed SERCA 2b with ERp57. We found that coexpression reduced the frequency of Ca2+ oscillations compared with overexpression of SERCA 2b by itself. A histogram of period and t1/2 shows that both were significantly prolonged suggesting that Ca2+ uptake into the ER is reduced (Fig. 1 A). Western blots demonstrated that expression levels of SERCA 2b were the same regardless of whether ERp57 was coexpressed with the pump (Fig. 1 B). These results are consistent with the hypothesis that ERp57 modulates ER thiol groups in SERCA 2b.

    Figure 1. ERp57 reduces the frequency of Ca2+ oscillations mediated by SERCA 2b. (A) Confocal images of Ca2+ oscillations in Xenopus oocytes expressing SERCA 2b alone (n = 22) or coexpressing ERp57 with SERCA 2b (n = 22). Traces represent changes in fluorescence (F/F) as a function of time. Each plot represents two independent experiments with 11 oocytes per group. Individual Ca2+ wave images are presented at the indicated time. The white square in each and subsequent images represents a 5 x 5 pixel area used in determining F/F. Histogram plots of the period between oscillations and the decay time (t1/2) are for individual oscillations at peak activity, defined as the highest frequency for a 100-s window of time. Asterisks indicate statistical significance (P < 0.05, t test). (B) Western blots of SERCA 2b and ERp57. One oocyte equivalent was loaded per lane and proteins were resolved through 10% SDS-PAGE. SERCA 2b migrates 110 kD and ERp57 60 kD as expected. The loading control lane in each and subsequent gels represents an invariant Xenopus protein that migrates at 42 kD. These gels represent three independent Western blots. Bar, 100 μm.

    L4 cysteine–deficient mutants of SERCA 2b exhibit higher frequency of Ca2+ oscillations

    To test whether the thiol groups in L4 are important in modulating Ca2+ oscillations enhanced by SERCA 2b, we imaged Ca2+ activity in oocytes overexpressing either the oxidizable form of SERCA 2b or two L4 cysteine–deficient mutants (SERCA 2b-C1SC2S and SERCA 2b-C1AC2A) that cannot form a disulfide bond and are a constitutively reduced form. Because these mutants did not express as efficiently as SERCA 2b in oocytes, we lowered expression levels of the pump to match expression levels of the mutants (Fig. 2 A). Under these conditions, we found that both mutants exhibited a higher frequency of Ca2+ oscillations and more rapid cytosolic Ca2+ uptake (i.e., shorter t1/2) than SERCA 2b (Fig. 2 B). We also overexpressed a single missense mutation found in a Darier disease pedigree that involves a cysteine to glycine mutation in L4 (SERCA 2b-C875G; Ruiz-Perez et al., 1999; Sakuntabhai et al., 1999; Ahn et al., 2003). When overexpressed in the oocytes, this mutant also exhibited a higher frequency of Ca2+ oscillations than the wild-type SERCA 2b (unpublished data). Together, with the previous data, our results suggest that ERp57 promotes disulphide bond formation in L4, thereby reducing the activity of the Ca2+ pump. When the disulfide bridge in L4 is disrupted, the Ca2+ ATPase appears to exhibit higher pump activity.

    Figure 2. L4 cysteine–deficient mutants of SERCA 2b exhibit higher frequencies of Ca2+ oscillations. (A) Western blots of SERCA 2b and L4 mutants were loaded as follows: (lane 1) SERCA 2b, (lane 2) SERCA 2b-C1SC2S and (lane 3) SERCA 2b-C1AC2A. Two oocyte equivalents were loaded per lane and proteins were resolved through 12% SDS-PAGE. Gels represent four independent Western blots. (B) Confocal images of Ca2+ oscillations are shown in oocytes expressing SERCA 2b (n = 34) or the L4 cysteine–deficient mutants SERCA 2b-C1SC2AS (n = 40) and SERCA 2b-C1AC2A (n = 38). Traces represent two independent experiments with 15–20 oocytes per group. Histogram plots t1/2 for (1) SERCA 2b, (2) SERCA 2b-C1SC2S, and (3) SERCA 2b-C1AC2A expressing oocytes. Asterisks indicate statistical significance (P < 0.05, t test) between SERCA 2b and each mutant group. Bar, 100 μm.

    Characterization of the catalytic activity of ERp57 and its mutants

    Two conserved thioredoxin motifs in ERp57 are thought to be responsible for catalytic activity of the enzyme (Hirano et al., 1995). One motif is positioned near the NH2-terminus (T1) and the other is near the COOH-terminus (T2). Two single mutants, ERp57-T1 and ERp57-T2, and a double mutant, ERp57-T1T2, were generated by mutagenesis of the relevant cysteines into serines in each motif (Fig. 3 A). To characterize the mutant ERp57 proteins, we generated GST fusion proteins and measured in vitro the catalytic activity using an insulin turbidity assay (Holmgren, 1979; Hirano et al., 1995). Protein disulfide isomerase (PDI), another ER resident oxidoreductase, was used as a positive control for this assay. We cloned the rat isoform and made purified GST-PDI. Both GST-PDI and GST-ERp57 exhibited strong enzymatic activity, although the latter exhibited slower kinetics. In comparison to ERp57, the ERp57-T2 mutant exhibited 70% activity, whereas the ERp57-T1 mutant exhibited only 30% activity. The double mutation ERp57-T1T2 completely abolished ERp57 enzymatic activity. There was no activity when GST alone or enzyme was absent in the assay (Fig. 3 B). Purified GST and GST fusion proteins are shown (Fig. 3 C). Together, these results suggest that the T1 motif plays a critical role in ERp57 enzymatic activity.

    Figure 3. Enzymatic activity of ERp57 and mutants measured in vitro. (A) ERp57 mutants lacking thioredoxin motifs. Two conserved WCGHCK motifs of ERp57 are thought to be the active sites for thiol-dependent oxidoreductase activity. Cysteines in each motif are indicated in black circles. Mutagenesis of relevant cysteines into serines is indicated by white circles. (B) Thiol-dependent catalytic activity of GST-PDI (positive control) and GST-ERp57 or mutant GST-ERp57 fusion proteins measured in vitro by the insulin turbidity assay at 300 μM . GST alone and lack of enzyme input are used as negative controls in this assay. Triplicate absorbanceOD 650 values were taken in three independent experiments and plotted as a function of time. Input amount of GST fusion proteins was 0.8 μM except for GST (22.04 μM). (C) Coomassie blue staining of GST and GST fusion proteins as labeled after one-step affinity purification. Proteins (5 μg each) were resolved through 12% SDS-PAGE.

    ERp57 catalytic activity correlates with the reduction in SERCA 2b activity

    To determine the relationship between ERp57 catalytic activity with Ca2+ pump activity, we coexpressed wild-type or mutant ERp57 with SERCA 2b. As expected, ERp57 had the highest effect in reducing the frequency of Ca2+ oscillations (i.e., reduced pump activity). The ERp57-T2 mutant that had 70% enzymatic activity in the insulin assay exhibited intermediate levels of pump inhibition. Neither ERp57-T1 (30% enzyme activity) nor ERp57-T1T2 (devoid of enzyme activity) affected the Ca2+ wave period and t1/2 that was enhanced by SERCA 2b overexpression (Fig. 4, A and B). Western blots demonstrated that ERp57 and its mutants as well as SERCA 2b expression levels were similar throughout expression groups (Fig. 4 C). Independent confirmation that all ERp57 mutants were correctly processed in the ER was provided by in vitro translations supplemented with canine microsomes (Fig. 4 D). Together, these results strongly suggest that ERp57 oxidoreductase activity is responsible for the modulation of Ca2+ uptake by SERCA 2b.

    Figure 4. Enzymatic activity of ERp57 plays a critical role in modulating SERCA 2b. (A) Confocal images of Ca2+ oscillations shown in oocytes overexpressing proteins as labeled: SERCA 2b alone (n = 23); SERCA 2b + ERp57 (n = 24); SERCA 2b + ERp57-T1 (n = 20); SERCA 2b + ERp57-T2 (n = 23); and SERCA 2b + ERp57-T1T2 (n = 32). Traces represent two independent experiments with 11–15 oocytes per group. (B) Histograms of period and t1/2 for the experiment in A. Asterisks indicate statistical significance (P < 0.05, t test) between SERCA 2b and SERCA 2b + ERp57 or SERCA 2b + ERp57-T2. (C) Western blots of SERCA 2b and ERp57 from lysates of experimental oocytes. One oocyte equivalent was loaded per lane and proteins were resolved through 12% SDS-PAGE. Gels represent three independent Western blots. (D) In vitro translations of ERp57 and mutants in rabbit reticulocytes in the absence or presence of canine pancreatic microsomes. Note that the signal peptide was proteolytically cleaved in reactions supplemented with microsomes. This gel is representative of four independent experiments. Bar, 100 μm.

    The interaction between ERp57 and L4 is specific and Ca2+ dependent

    To investigate the interaction between ERp57 and its potential target L4, we performed an in vitro GST pull-down experiment under various Ca2+ concentrations: the highest being 300 μM to mimic full Ca2+ store content and the lowest being 10 μM to mimic Ca2+ store depletion. Interestingly, ERp57 binds to L4 in a Ca2+-dependent manner: the interaction is strongest at high Ca2+ (300 μM) and is significantly reduced at low Ca2+ (10 μM; Fig. 5 A). To test the specificity of this interaction we performed a similar GST pull-down experiment with GST-PDI. Neither GST-PDI nor GST alone interacted with the L4 (Fig. 5 B). This suggests that the interaction between ERp57 and L4 is specific. Moreover, this interaction occurs preferentially at high Ca2+ concentrations that are indicative of full Ca2+ stores (Pozzan et al., 1994).

    Figure 5. The interaction between ERp57 and L4 is Ca2+ dependent and specific. (A) GST pull-down assays performed at the indicated in micromolars. The gel is loaded as follows: input of in vitro–translated L4 (lane 1); pull downs for 30 μg GST control (lanes 2–5); pull downs for 10 μg GST-ERp57 (lanes 6–9). Proteins were resolved through 15% SDS-PAGE. L4 migrates 11 kD (109 aa). Data represent three independent experiments. Histogram depicts densitometric analysis from these experiments. L4 bands were normalized to the intensity of the band at 300 μM Ca2+. Asterisks indicate statistical significance (P < 0.05, one-way ANOVA). (B) The interaction between ERp57 and L4 is specific by GST pull-down assay. Lanes were loaded as follows: input of in vitro–translated L4 (lane 1); 30 μg GST negative control at the indicated (lanes 2 and 3); 10 μg GST-ERp57 (lanes 4 and 5); 10 μg GST-PDI (lanes 6 and 7). Proteins were resolved through 15% SDS-PAGE. The gel represents three independent experiments. (Right gel) Coomassie blue stain of 3 μg purified GST (lane 1); 1 μg GST-ERp57 (lane 2), and 1 μg GST-PDI (lane 3). Proteins were resolved through 13% SDS-PAGE. GST migrates 27 kD, and GST-ERp57 and GST-PDI migrate 80 kD (mature rPDI is 489 aa, mature hERp57 is 481 aa). The arrowheads correspond to L4. (C) The L4 protein localizes to the ER. (Top) Coexpression in Xenopus oocytes of GFP-L4 (green) with DsRed-IP3R (red). The IP3R is used as a marker of ER localization. The overlay (yellow) demonstrates that the L4 localizes in the ER. (Bottom) Cytosolic GFP (green) used a negative control, is coexpressed with DsRed-IP3R (red). Note that the cytosolic GFP expression pattern is more diffused than that of the GFP-L4 and that there is no overlap of the two proteins indicating lack of colocalization. High magnification of the small square regions are shown as insets in each figure. Bar, 5 μm.

    Translational scanning studies of SERCAs indicate that they have intrinsic sequences that determine topologic insertion into the ER membrane (Bayle et al., 1995, 1997). To ascertain that the L4 construct was correctly inserted into the ER, a GFP-L4 fusion construct was coexpressed in Xenopus oocytes with a marker for ER localization, a DsRed-IP3R fusion protein. As a control, cytosolic GFP was also coexpressed with DsRed-IP3R. As expected, GFP-L4 colocalized with the IP3R, whereas GFP had a more diffused cytosolic expression pattern (Fig. 5 C). These data indicate that the L4 construct was correctly localized in the ER.

    ERp57 and PDI catalytic activity lack Ca2+ dependence

    Because the association of ERp57 with the L4 substrate is stronger at higher Ca2+ concentrations, we tested whether the intrinsic activity of ERp57 is Ca2+ dependent. We measured in vitro the catalytic activity of purified GST-ERp57 at the same range of used in the GST pull-down assay (300, 150, 50, and 10 μM). The activity of ERp57 was only mildly but not significantly dependent on Ca2+ at the concentrations measured (Fig. 6 A). A similar assay was also performed for GST-PDI and in this case we found no Ca2+ dependence of its activity (Fig. 6 B).

    Figure 6. The catalytic activity of ERp57 and PDI is Ca2+ independent. Enzymatic activity is measured using the insulin turbidity assay at the indicated Ca2+ concentrations. AbsorbanceOD 650 values were collected in triplicate and plotted. These plots represent four independent experiments. The standard error bars were smaller than the size of the symbols. Input amounts of GST-ERp57 and GST-PDI fusion proteins was 0.8 μM.

    The effects of ERp57 on Ca2+ wave activity are specific for the SERCA 2b isoform

    CRT and CLNX inhibit Ca2+ oscillations via an interaction with the COOH-terminal sequence of SERCA 2b where a glycosylation consensus motif exists (John et al., 1998; Roderick et al., 2000). Furthermore, CRT does not interact with SERCA 2a, which lacks the 11th transmembrane segment and a COOH terminus in the ER lumen (John et al., 1998). ERp57 binds to CRT's P domain (Zapun et al., 1998; Oliver et al., 1999; Frickel et al., 2002; Leach et al., 2002). Based on these observations, we hypothesized that CRT binds the COOH-terminal sequence of the pump and recruits ERp57 to modulate L4 thiol groups and consequently pump activity. Because SERCA 2a also has the L4, we tested whether ERp57 modulates SERCA 2a directly or whether the effects are specific to SERCA 2b via CRT. We coexpressed ERp57 with SERCA 2a and found that ERp57 does not modulate Ca2+ oscillations in oocytes overexpressing this pump isoform (Fig. 7 A). We also coexpressed ERp57 with two mutants that eliminated the consensus glycosylation motif in SERCA 2b (SERCA 2b-N1036A and SERCA 2b-S1038A). We find that ERp57 does not modulate Ca2+ oscillations mediated by these two pump mutants (Fig. 7 B). Histograms of period and t1/2 are shown in Fig. 7 C, whereas Western blots for these experiments are shown in Fig. 7 D. Together, these experiments demonstrate that CRT is required to recruit ERp57 to the L4.

    Figure 7. ERp57 does not affect Ca2+ oscillations mediated by SERCA 2a, nor SERCA 2b glycosylation motif mutants. (A) Confocal images of Ca2+ oscillations in oocytes overexpressing SERCA 2b (n = 31), SERCA 2b + ERp57 (n = 39), SERCA 2a (n = 25), and SERCA 2a + ERp57 (n = 30). The traces represent two independent experiments with 12–20 oocytes per group. (B) Images of Ca2+ oscillations in oocytes overexpressing SERCA 2b-N1036A (n = 34), SERCA 2b-N1036A + ERp57 (n = 15), SERCA 2b-S1038A (n = 37), and SERCA 2b-S1038A + ERp57 (n = 16). The traces represent two independent experiments with 8–19 oocytes per group. (C) Histograms plot period and t1/2 for experiments in A and B, respectively. Asterisks indicate statistical significance (P < 0.05, t test) between SERCA 2b with SERCA 2b + ERp57 oocytes. (D) Western blots of SERCA 2a, SERCA 2b, or its mutants, and ERp57 from lysates of experimental oocytes as labeled. One oocyte equivalent was loaded per lane and proteins were resolved through 12% SDS-PAGE. Arrowheads indicate the protein as labeled at the top of each gel Bars: (A and B) 100 μm.

    Mechanism of ERp57 modulation of Ca2+ oscillations

    The globular domain of CRT comprises the N and C domains and interacts with substrate glycoproteins, whereas the tip of the P domain binds to ERp57 and promotes disulfide bond formation (Ellgaard et al., 2001, 2002; Schrag et al., 2001; Frickel et al., 2002; Leach et al., 2002). Previous observations from our group demonstrated that CRT-NP (i.e., CRT lacking the C domain) modulated SERCA 2b just like wild-type CRT, indicating that in this case the C domain might not be necessary for the interaction (Camacho and Lechleiter, 1995; John et al., 1998). Thus, CRT most likely targets the COOH-terminal sequence of SERCA 2b via its N domain, whereas the P domain recruits ERp57 to interact with the L4. To test this hypothesis, we overexpressed four dominant negative constructs (L4, CRT-NC, CRT-N, or CRT-P) to determine whether they would interrupt the interaction between endogenous SERCA 2b with the ERp57–CRT complex. We found that oocytes overexpressing these four constructs exhibited shorter t1/2 values (faster SERCA 2b activity) than control oocytes. In contrast, oocytes overexpressing CRT or CRT-NP exhibited longer t1/2 values, consistent with previous findings (Camacho and Lechleiter, 1995; John et al., 1998; Fig. 8).

    Figure 8. Overexpression of L4, NC, N, or P domains of CRT increase Ca2+ oscillation frequency. Representative confocal images of Ca2+ oscillations in oocytes as labeled: H2O (n = 46); L4 (n = 31); CRT (n = 22); CRT-NP (n = 28); CRT-NC (n = 28); CRT-N domain (n = 45); and CRT-P domain (n = 49). Two independent experiments with 11–25 oocytes per group were performed. Histogram plots t1/2 of individual waves normalized to the H2O control group. Asterisks indicate statistical significance (P < 0.05, t test) between L4, CRT, CRT-NP, CRT-NC, CRT-N, CRT-P, and the control group. Bar, 100 μm.

    To determine the specificity of these dominant negative constructs for SERCA 2b, we also coexpressed them with either SERCA 2a or SERCA 2b. Oocytes coexpressing L4, CRT-NC, CRT-N, or CRT-P with SERCA 2b exhibited significantly shorter t1/2 values than SERCA 2b overexpressing oocytes, consistent with our observations presented in the previous paragraph. Note that control oocytes coexpressing CRT with SERCA 2b exhibited the longest t1/2 values (lowest frequency of Ca2+ oscillations; Camacho and Lechleiter, 1995; Fig. 9, A and B). In agreement with the results reported in Fig. 7, we found that Ca2+ oscillations enhanced by SERCA 2a were not affected by coexpression with these constructs (Fig. 9 C). Together, these data support our model that CRT recruits ERp57 to the lumenal L4 in SERCA 2b, modulating pump activity to maintain ER Ca2+ homeostasis (Fig. 10).

    Figure 9. Dominant negative constructs increase the frequency of Ca2+ oscillations enhanced by SERCA 2b, but not SERCA 2a. (A) Confocal images of Ca2+ oscillations in Xenopus oocytes overexpressing SERCA 2b (n = 22); or coexpressing SERCA 2b with L4 (n = 22); CRT (n= 22); CRT-NC (n = 21); CRT-N (n = 21); and CRT-P (n = 21) are shown. Two independent experiments with 10–11 oocytes per group were performed. (B) Histogram plots t1/2 of individual waves. Asterisks indicate statistically significant difference (P < 0.05, t test) between L4, CRT, CRT-NC, CRT-N, and CRT-P with respect to the SERCA 2b (S2b) overexpression. (C) Histogram shows the result of a similar experiment performed for SERCA 2a. Confocal images of Ca2+ oscillations in oocytes overexpressing SERCA 2a (n = 21) or coexpressing SERCA 2a with L4 (n = 20); CRT (n = 20); CRT-N (n = 20); CRT-P (n = 20); and CRT-NC (n = 20) are not depicted. Note that on the same y-axis scale as in experiment in B, none of the tested constructs display a significant difference with respect to SERCA 2a (labeled S2a). Bar, 100 μm.

    Figure 10. Model depicting the functional consequences of the interaction between ERp57–CRT with SERCA 2b. At rest, the ER Ca2+ stores are full (high ER), the N domain of CRT interacts with the COOH-terminal sequence of SERCA 2b, whereas the P domain recruits ERp57 to target L4 in SERCA 2b. At high ER our data suggest that ERp57 promotes disulfide bond formation between thiol groups in the loop, reducing pump activity (i.e., decreasing the frequency of Ca2+ oscillations and t1/2). This activity of ERp57 favors disulfide bond formation because the prevailing conditions in the ER are relatively oxidizing. As ER decreases below 50 μM, ERp57 dissociates from L4, allowing SERCA 2b in its reduced form (cysteine mutagenesis) to be more active. Thus, at low ER SERCA 2b favors ER store refilling. The arrow indicates the point of divergence between SERCA 2a and SERCA 2b. NFS is the glycosylation consensus motif at the COOH-terminal sequence of SERCA 2b.

    Discussion

    It is well established that CRT or CLNX form a macromolecular complex with ERp57 to assist in glycoprotein folding. In particular, CRT interacts with targeting glycoproteins via its globular domain, whereas the tip of the P domain recruits ERp57 to the glycoprotein substrate to promote intra/inter disulfide bond formation (High et al., 2000; Ellgaard et al., 2001, 2002; Schrag et al., 2001, 2003; Frickel et al., 2002; Leach et al., 2002; Ellgaard and Helenius, 2003; Kostova and Wolf, 2003). From our work using the Ca2+ oscillation assay in Xenopus oocytes, we have found that both the N and P domains of CRT are necessary for inhibition of Ca2+ oscillations enhanced by SERCA 2b, whereas the C domain is not required (Camacho and Lechleiter, 1995; John et al., 1998; Roderick et al., 2000). In this paper, we are led to the conclusion that CRT uses the N domain to target the COOH-terminal sequence of SERCA 2b, and the P domain to recruit ERp57 to interact with the L4 of SERCA 2b. Several of our findings support this conceptual model. ERp57 does not affect Ca2+ oscillations enhanced by SERCA 2a, nor SERCA 2b mutants defective in the COOH-terminal glycosylation motif. Overexpression of L4 or the NC, N, or P domains of CRT exhibit dominant negative effects that presumably act by disrupting the interaction between the endogenous CRT–ERp57 complex and SERCA 2b. In particular, overexpression of the first construct, L4, should bind endogenous ERp57 preventing it from regulating the pump. The second construct, CRT-NC, contains the entire globular domain that binds the glycosylated NFS motif of SERCA 2b, but lacks the ability to recruit ERp57 (Schrag et al., 2001; Leach et al., 2002). Its overexpression should compete with the interaction of endogenous CRT with SERCA 2b, thereby preventing ERp57 from regulating pump activity. The third construct, CRT-N, contains two residues that are responsible for binding glucose (Schrag et al., 2001). Its overexpression has the same effect as CRT-NC, indicating that this construct is sufficient to target the SERCA 2b COOH-terminal sequence. The fourth construct, CRT-P, contains the repeat known as 1112, which is longer than the fragment used by Ellgaard and colleagues (Ellgaard et al., 2002), who found that a shorter fragment (repeat 112) was sufficient to interact with ERp57. Without the globular NC domain, the P domain itself is unable to target the glycan (Leach et al., 2002). Consequently, overexpression of CRT-P should bind endogenous ERp57 and prevent regulation of SERCA 2b.

    ERp57 and its homologue PDI have different substrate specificities (Freedman et al., 2002; Clissold and Bicknell, 2003). ERp57 specifically associates with N-linked glycoproteins, whereas PDI does not. This specificity is mainly mediated by an interaction with CRT or CLNX (Oliver et al., 1997, 1999; Van der Wal et al., 1998; Zapun et al., 1998; High et al., 2000; Frickel et al., 2002). Using in vitro GST pull-down experiments, we also demonstrated that ERp57 specifically interacts with the L4 of SERCA 2b, whereas PDI did not. It is possible that there is a direct interaction between ERp57 and L4, but it is equally likely that an indirect protein interaction is occurring in a pull-down assay. For example, microsomes contain CRT and glycoproteins (e.g., SERCA 2b), which could then link ERp57 to L4. In fact, the bulk of our results favor the requirement of CRT to recruit ERp57 to the L4.

    The mechanisms that regulate SERCA activity from the ER have been until now somewhat unclear. Decreased lumenal Ca2+ induces a strong stimulation of SERCA activity in isolated pancreatic acinar cells (Mogami et al., 1998). We demonstrate that the association of ERp57 with the L4 is Ca2+ dependent in the physiological range of ER lumenal Ca2+ (10, 50, 150, and 300 μM). The Ca2+ dependency of the association between ERp57 and L4 is likely to be mediated by CRT, because Ca2+ does not regulate the intrinsic enzyme activity of the ERp57. It has been reported that Ca2+ is required for CRT binding to oligosaccharides, although these experiments were conducted beyond physiological (10 mM Ca2+; Vassilakos et al., 1998). Ca2+ has also been shown to modulate the interaction between CRT and ERp57 (Corbett et al., 1999). Together, our data suggest the following role of ER Ca2+ in the feedback mechanism that regulates SERCA 2b activity (Fig. 10). When ER Ca2+ stores are full (300 μM Ca2+), ERp57 binds to L4 promoting disulfide bond formation in the loop, which inhibits pump activity. When Ca2+ stores become depleted (10 μM Ca2+), ERp57 dissociates from L4, resulting in the reduced form of SERCA 2b that is more active. The mechanism by which thiol groups in the L4 are reduced after ERp57 dissociates from the pump is unknown. The ER lumen maintains a neutral to slightly oxidized environment (GSH–GSSG 1–3; Hwang et al., 1992). Our results suggest that ERp57 must be bound to L4 in order to maintain it in an oxidized state. It is possible that additional ER proteins play a role here. Regardless of the precise underlying mechanism, our data clearly indicate that the reduced form of L4 supports higher pump activity to rapidly refill the ER.

    The CLNX–CRT cycle has a well-established role in productive glycoprotein folding and quality control of nascent glycoproteins undergoing folding (High et al., 2000; Ellgaard and Helenius, 2003; Kostova and Wolf, 2003; Schrag et al., 2003). Our observations indicate that these ER chaperones interact with a mature ER resident glycoprotein (SERCA 2b). Association/dissociation of other ER chaperones with mature proteins has also been reported during the unfolded protein response (Bertolotti et al., 2000). We speculate that the classical CLNX–CRT cycle and the system we have characterized here exist in parallel and that the action of CRT–CLNX on SERCA 2b provides the homeostatic feedback necessary to maintain Ca2+ conditions that promote productive glycoprotein folding. Without it, Ca2+ depletion could result in the well-known unfolded protein response, which can bring about cellular apoptosis under certain stress conditions (Kaufman, 1999; Welihinda et al., 1999; Patil and Walter, 2001; Harding et al., 2002). Maintaining optimal Ca2+ concentrations in the ER is clearly important for nascent protein folding (Hardman and Wetmore, 1996; Chen et al., 1997; Stevens and Argon, 1999; Ramsden et al., 2000). The ability of the lectin chaperones to "talk" to a mature protein in the Ca2+ signaling machinery provides the mechanism by which the optimal Ca2+ environment is maintained for protein folding.

    Oxidant treatment inactivates SERCA 2b to a greater extent than other pump isoforms (Grover et al., 1997; Barnes et al., 2000). Our observations imply that SERCA 2b is in fact a redox sensor. In the oxidized state of L4, this pump exhibits lower activity. On the other hand, the pump favors rapid Ca2+ uptake in the L4 mutants that are constitutively reduced by cysteine mutagenesis. Interestingly, the ryanodine receptor, a Ca2+ release channel located on the SR–ER is also a redox sensor (Zable et al., 1997; Xia et al., 2000; Sun et al., 2001). The oxidized channel correlates with the open state, whereas the reduced form correlates with channel closure. The IP3R may also sense the redox potential because it contains cysteines in the ER lumenal facing loop that line the channel pore. Consequently, modulation of redox potential of reactive thiols in the ER might be a general mechanism by which SERCA 2b, IP3R, and ryanodine receptor control ER Ca2+. In terms of Ca2+ homeostasis, our observations with ERp57 fit the view that ER redox modulates Ca2+ release and uptake in coordinate and opposite directions. In particular, oxidization appears to favor Ca2+ release by opening Ca2+ channels and inhibiting Ca2+ pumping. On the other hand, reduction seems to favor Ca2+ uptake by channel closure and increasing Ca2+ pumping. The combined effect of these two actions helps to minimize the loss of ER Ca2+ and maximize refilling of the stores, thereby protecting the physiological functions of the ER such as glycoprotein folding.

    Materials and methods

    Vectors and reagents

    The Xenopus expression vectors for rat SERCA 2a and SERCA 2b have been described previously (John et al., 1998). L4 cysteine–deficient mutants of SERCA 2b were generated as follows: cysteines 875 and 887 were mutated to serines (mutant SERCA 2b-C1SC2S) or to alanines (mutant SERCA 2b-C1AC2A). A two-step mutagenesis protocol was performed. To generate the SERCA 2b-C1SC2S mutation primers 5'-GCTGAGTCATTTCCTGCAGTCAAAGGAGGACAACCC-3' and 5'-CCAGACTTCGAAGGAGTGGATTCAGCAATCTTTGAGTCCC-3' with their respective reverse complement primers were used. Primers 5'-GCTGAGTCATTTCCTGCAGGCTAAGGAGGACAACCC-3' and 5'-CCAGACTTCGAAGGAGTGGATGCTGCAATCTTTGAGTCCC-3' and their respective reverse complement primers were used for the SERCA 2b-C1C2A mutant. Plasmid pHN-SERCA 2b-C875G was generated using the forward primer 5'-GCTGAGTCATTTCCTGCAGGGTAAGGAGGACAACCC-3' and its reverse complement. Plasmid pHN-SERCA 2b-N1036A has been generated and published previously (John et al., 1998). Mutant SERCA 2b-S1038A (plasmid pHN SERCA 2b-S1038A) was generated by PCR using the forward primer 5'-AGCACAGACACTAACTTTGCTGATATGTTCTGG-3' and the reverse primer 5'-CCAGAACATATCAGCAAAGTTAGTGTCTGTGCT-3'.

    A construct encoding the L4 of SERCA 2b was generated by PCR amplification spanning methionine 814 and arginine 922 with primers 5'-ACTGGGATCCATGAACAAACCCCCACGGAACCCA-3' and 5'-ACTGAAGCTTTTACCTCAGCAGGGACTGGTTTTC-3'. The PCR product was ligated into the BamHI and HindIII sites of the similarly digested vector pHN (plasmid pHN-SERCA 2b-L4). To generate plasmid pHN-GFP-L4, a BamHI fragment from pHN-GFP-S65T-TAA, as described previously (John et al., 1998), was subcloned into plasmid pHN-SERCA 2b-L4 that was digested with BamHI and treated with calf intestinal phosphatase. Plasmid pHN-GFT S65T was generated previously (John et al., 1998). The Xenopus expression vector of DsRed-IP3R was generated by a three-step PCR protocol to create a fusion of DsRed to the NH2-terminal sequence of the IP3R. First, the full-length DsRed was amplified by PCR from the template of pDSRed 1-N1 (CLONTECH Laboratories, Inc.). The forward and reverse primers were 5'-ACTGGAATTCATGGTGCGCTCCTCCAAGAACGTC-3' and 5'-AAGAAAGCTGGACATTTCATTCATCAGGAACAGGTGGTGGCGGCC-3'. Second, the NH2 terminus of IP3R was amplified by PCR from template pHN-IP3R with the forward and reverse primers as 5'-GGCCGCCACCACCTGTTCCTGATGAATGAAATGTCCAGCTTTCTT-3' and 5'-GTGCACATGTAGCATCAGGTGGCAGAATGA-3'. The purified PCR products served as templates to create the final product DsRe-IP3R. In this PCR reaction, the forward and reverse primers were 5'-ACTGGAATTCATGGTGCGCTCCTCCAAGAACGTC-3' and 5'-GTGCACATGTAGCATCAGGTGGCAGAATGA-3'. The final PCR fusion product was digested with EcoRI and NsiI and subcloned into the EcoRI and NsiI sites of PHN-IP3R.

    The Xenopus expression vector of ERp57 (plasmid pHN-ERp57) was generated in a three-step PCR protocol. First, the mature human ERp57 was amplified from the template pET9-ERp613 (a gift from D.Y. Thomas, Biotechnology Research Institute, Montréal, Canada) with primers 5'-CTGCTCGGCCTGGCCGCCGCCTCCGACGTGCTAGAACTCACG-3' and 5'-ACGTAAGCTTTTAGAGATCCTCCTGTGCCTTCTT-3'. A second PCR generated the signal peptide of CRT from the template pHN-CRT (Camacho and Lechleiter, 1995) using primers 5'-TAATACGACTCACTATAGGG-3' and 5'-CGTGAGTTCTAGCACGTCGGAGGCGGCGGCCAGGCCGAGCAG-3'. The purified PCR products served as templates to generate a fusion of the CRT signal peptide and mature ERp57. In this PCR reaction, the forward and reverse primers were 5'-TAATACGACTCACTATAGGG-3' and 5'-ACGTAAGCTTTTAGAGATCCTCCTGTGCCTTCTT-3'. The final PCR fusion product was subcloned into the HindIII and SSTI sites of the Xenopus expression vector pHN. Three mutants of ERp57 were generated. The first mutant had cysteines 57 and 60 mutated to serines in the NH2-terminal thioredoxin motif (mutant ERp57-T1) and was generated by PCR using primer 5'-CGAGTTCTTCGCTCCCTGGTCTGGACACTCCAAGAGACTTGCACC-3' and its reverse complement. The second construct had cysteines 406 and 409 in the COOH-terminal thioredoxin motif mutated to serines (mutant ERp57-T2) and was generated using primer 5'-GAATTTTATGCCCCTTGGTCTGGTCATTCTAAGAACCTGGAGCCC-3' and its reverse complement. The third construct was a double mutant generated in two PCR steps with the above primers (mutant ERp57-T1T2).

    Rat PDI cDNA was cloned from a rat liver cDNA library (Invitrogen) by PCR using primers 5'-ACTGGGATCCATGCTGAGCCGTGCTTTGCTGTGC-3' and 5'-ACTGTCTAGACTACAGTTCATCCTTCACGGC-3' based on the GenBank/EMBL/DDBJ accession no. X02918. The PCR product was subcloned into the BamHI and XbaI sites of pHN and fully sequenced.

    To obtain GST-ERp57 fusion proteins including wild type and mutants as well as GST-PDI, we amplified the corresponding mature cDNA fragments by PCR and subcloned them into pGEX-4T-2 vector (Amersham Biosciences). For ERp57 and its mutants, the primers were 5'-TCGAGGATCCATGTCCGACGTGCTAGAACTCACG-3' and 5'-ACTGCTCGAGTTAGAGATCCTCCTGTGCCTTCTT-3', whereas for PDI, the primers were 5'-ACTGGGATCCATGGACGCTCTGGAGGAGGAGGAC-3' and 5'-ACTGCTCGAGCTACAGTTAATCCTTCACGGC-3'. The PCR products were ligated into the BamHI and XhoI sites of pGEX-4T-2.

    The Xenopus vectors encoding CRT, CRT-NP, CRT-NC, and CRT-N domains have been published previously (Camacho and Lechleiter, 1995). The construct for expression of the P domain (plasmid pHN-CRT-P) was generated by PCR mutagenesis designed to remove the N domain from template pHN-CRT-NP (Camacho and Lechleiter, 1995). The primers used had sequence 5'-GCCGCCGAGCCCGATGACTGGGACTTCCTACCCCCCAAGAAGATAAAGGACCCA-3' and 5'-TGGGTCCTTTATCTTCTTGGGGGGTAGGAAGTCCCAGTCATCGGGCTCGGCGGC-3'. The resulting construct contains the CRT signal peptide followed by the P domain (amino acids 181–260) and a KDEL sequence for ER retention.

    Automatic sequencing of all cDNA constructs was performed at the UTHSCSA Advance Nucleic Acid Core Facility. All primers were purchased from Operon Technologies (QIAGEN). Unless otherwise specified, all chemicals were purchased from Sigma-Aldrich and all restriction enzymes were purchased from Invitrogen Life Technologies.

    In vitro transcriptions and translations

    Synthetic mRNA was prepared as described previously (Camacho and Lechleiter, 1995). In vitro translations were performed as described previously (Roderick et al., 2000).

    Western blots

    Oocytes extracts were prepared as described previously (Camacho and Lechleiter, 1995). In brief, 5–10 oocytes were pooled and homogenized in buffer containing 20 mM Tris-HCl, pH 7.6, 140 mM NaCl, 250 mM sucrose, and protease inhibitors in a mix containing 0.2 mM AEBSF, 10 μM leupeptin, 1 μM pepstatin A, and 0.8 mM benzamidine (Calbiochem). After centrifugation at 4,500 g for 15 min at 4°C, the supernatant was ultracentrifuged at 125,000 g for 20 min at 4°C. Microsomal pellets were resuspended in solubilization buffer (10 mM Tris-HCl, pH 7.6, 140 mM NaCl, 1% Triton X-100, and protease inhibitors). A second centrifugation (15,000 g for 10 min) was performed to discard the insoluble material. SDS-PAGE was performed by loading 1–2 oocyte equivalents per lane and transferred to nitrocellulose. A polyclonal rabbit anti-SERCA antibody ( NI, 1:8,000 dilution, a gift from J. Lytton, University of Calgary, Calgary, Canada) was used to detect SERCA 2b. A rabbit anti-ERp57 polyclonal antibody (1:4,000 dilution, a gift from S. High, University of Manchester, Manchester, UK) was used to detect ERp57. HRP-conjugated donkey anti–rabbit IgG secondary antibodies (Jackson ImmunoResearch Laboratories) in a dilution of 1:10,000 were used in all Western blots and visualized by ECL (PerkinElmer Life Sciences, Inc.).

    GST fusion protein purification

    BL21 bacteria transformed with pGEX-4T-2, pGEX-4T-2-PDI or pGEX-4T-2-ERp57 (and mutants) were grown to OD 600 nm 0.6. Isopropyl-?-D-thiogalactopyranoside (Research Products International Corp.) was added to a final concentration of 1 mM to induce protein expression for 4 h at 37°C. Bacteria were lysed by sonication in 1x PBS containing 100 mM EDTA and a mix of protease inhibitors including (200 μM AEBSF, 10 μM leupeptin, and 1.5 μM pepstatin A) and 0.8 mM benzamidine. Bacterial lysates were centrifuged at 22,000 g and the supernatant collected. Binding of GST or GST fusion proteins to glutathione-Sepharose 4B (Amersham Biosciences) was performed at 4°C for 1 h followed by three washes with equilibration buffer (0.5 M Tris-HCl, pH 8.0, 4 mM EDTA, 0.1% ?-ME, 5% glycerol). Elution of bound protein was performed in this buffer supplemented with 15 mM glutathione. Proteins were dialysed against 0.05 M Tris-HCl, pH 7.5, containing 1 mM EDTA, 0.2% ?-ME, and stored at –80°C.

    GST pull-down assays

    In vitro translation of L4 was accomplished in a rabbit reticulocyte lysates supplement with canine pancreatic microsomes (both from Promega) and L-methionine (PerkinElmer Life Sciences). Microsomes were isolated and resuspended in solubilization buffer (10 mM Tris-HCl, pH 7.6, 140 mM NaCl, 1% Triton X-100 and a mixture of the protease inhibitors described in Western blots). Binding of in vitro–translated L4 to GST-ERp57 fusion protein(s) was performed at 4°C overnight in the presence of glutathione Sepharose 4B (Amersham Biosciences) in binding solution containing in mM 10 Tris-HCl, pH 8.0, 70 KCl, 2 MgCl2, 50 μM EGTA, 5% BSA, and protease inhibitors supplemented with experimental CaCl2 concentrations (60, 100, 200, and 350 μM). Proteins bound to glutathione Sepharose beads were washed three times in buffer containing 0.2 M Tris-HCl, pH 8.0, 0.1% Triton X-100, 70 mM KCl, 2 mM MgCl2, 50 μM EGTA, protease inhibitors, and corresponding CaCl2 concentrations. Proteins were resolved by 15% SDS-PAGE and visualized by autoradiography. Ca2+ concentrations were calculated according to existing algorithms (Fabiato and Fabiato, 1979).

    Insulin turbidity assay

    The insulin turbidity assay was performed as described previously (Holmgren, 1979; Hirano et al., 1995). In this assay, oxidized insulin was used as substrate to measure thiol-dependent reductase activity of ERp57. Under reducing conditions, the two interchain disulphide bonds of insulin are cleaved, resulting in the formation of a white insoluble precipitate. 10 mg/ml of insulin (Sigma-Aldrich) stock solution was prepared as described previously (Holmgren, 1979). In brief, 100 mg of insulin was first resuspended in 8 ml 0.05 M Tris-HCl, pH 8.0. Subsequently, the pH was adjusted between 2.0 and 3.0 by adding 1 M HCl and rapidly titrated to pH 8.0 with 1 M NaOH. The final volume of the solution was adjusted to 10 ml with H2O. The clear stock solution was stored at –20°C. On the experimental day, the insulin stock solution was diluted to 1 mg/ml with a buffer containing in 100 mM KAC, pH 7.5, and 2 mM EDTA, supplemented with CaCl2 concentrations (2.44, 2.28, 2.17, and 2.12 mM) to yield free of 300, 150, 50, and 10 μM. The final reaction volume was adjusted to 1 ml after purified ERp57 or its mutants were added. The reaction was initiated by adding 3 μl of 100 mM DTT. Abs650 nm was measured every 5 min in a BioSpec-1601 spectrophotometer (Shimadzu). Enzyme activity was defined by measuring the slope of the linear portion of the absorbance curve. Ca2+ concentrations were calculated according to known algorithms (Fabiato and Fabiato, 1979).

    Oocyte methods and confocal imaging

    Stage VI–defolliculated oocytes were injected a bolus of 50 nl of 1 μg mRNA using a standard positive pressure injector (Drummond Scientific). Oocytes were cultured in 50% L-15 media (Invitrogen) for 5–7 d at 18°C. Intracellular Ca2+ was imaged as described previously (Roderick et al., 2000). Oocytes were injected with fluorescent Ca2+ indicator Oregon green II (12.5 μM final; Molecular Probes) 30–60 min before imaging. Ca2+ release was initiated by injecting a 50 nl bolus of 6 μM IP3 (Calbiochem) to yield 300 nM final concentration. Imaging was performed in ND96 buffer containing 1 mM EGTA. Images were acquired at a rate of 0.75 s /frame on a confocal laser scanning microscope (model PCM2000; Nikon) using a 10x objective (NA = 0.45) at zoom 1.

    To characterize the ER localization of L4, GFP-L4 was coexpressed in oocytes with DsRed-IP3R. Fluorescence was monitored using a confocal microscope (model Fluoview 500; Olympus). GFP-L4 as well as GFP (as a negative control) were detected using a 488-nm laser line for excitation and a combination of a 510-nm long pass and a 550-nm short pass barrier filter for signal emission. DsRed fluorescence was obtained with a 568-nm laser line for excitation and a 585-nm long pass barrier filter for emission. Emission signals were collected using a 60x oil (NA = 1.4) objective (Olympus) at zoom 5.

    Imaging analysis

    The analysis of Ca2+ images was performed using the public domain NIH ImageJ program (developed at the National Institutes of Health and available at http://rsb.info.nih.gov/ij/).

    Statistical analysis

    Statistical significance was determined by t test or one-way ANOVA as appropriate and accepted at P < 0.05.

    Acknowledgments

    We wish to thank David Y. Thomas for the cDNA encoding mature human ERp57, Stephen High for rabbit ERP57 antibody, and Johnathan Lytton for rabbit SERCA 2 antibody. We also thank James Lechleiter, Da-Ting Lin, and Marianna Bollo for critical reading of the manuscript.

    This work was funded by National Institutes of Health grant R01 GM55372 to P. Camacho.

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