Modeling distinct compartments
http://www.100md.com
《细胞学杂志》
Heinrich and Rapoport (page 271) have used mathematical modeling to generate the first explanation of how a bidirectional transport system can generate unique compartments, such as the ER and Golgi, despite constant vesicle movement between them. The model provides testable predictions about the vesicle transport system in cells.In modeling a two-organelle system, the team found that they only needed to include two molecular components of the vesicle transport system: the coat proteins for budding; and the SNARE proteins for fusion. Coat proteins regulate budding from distinct compartments: COPI from the Golgi (to the ER); and COPII from the ER (to the Golgi). Meanwhile, SNARE proteins work in pairs, with a v-SNARE localized in the vesicle membrane and the t-SNARE in the target membrane. Different SNAREs direct vesicle fusion to specific organelles.
The new model only worked when it incorporated differential affinity of one coat protein for one set of SNARE proteins versus the other. If both coat proteins bound all SNAREs with equal affinity, then bidirectional vesicle transport would result in two uniform organelles. If the model assumed that one coat protein bound one pair of SNAREs with at least a 10-fold preference over the other SNARE pair, then the model accurately maintained two unique compartments.
One nonintuitive aspect of the model is that it predicts that both members of a SNARE pair, the v- and t-SNAREs, accumulate in the target compartment, a prediction borne out by experimental observations from other groups.
COPII is known to have high affinity for SNAREs that target the Golgi, and the model predicts that COPI should preferentially bind to ER SNAREs. If, however, the coat protein's binding affinity for a SNARE pair is too strong, then all of those SNARE proteins would accumulate in the target compartment, leaving vesicles to bud from the other compartment without any SNAREs that would allow it to fuse to the target membrane. The model also predicts that if one SNARE pair is overexpressed, then the size of its target compartment would increase.
Rbiya S. Tuma
rabiya@nasw.org
Reinhart Heinrich and Tom A. Rapoport
J. Cell Biol. 2005 168: 271-280.(Differential affinities between coats an)
The new model only worked when it incorporated differential affinity of one coat protein for one set of SNARE proteins versus the other. If both coat proteins bound all SNAREs with equal affinity, then bidirectional vesicle transport would result in two uniform organelles. If the model assumed that one coat protein bound one pair of SNAREs with at least a 10-fold preference over the other SNARE pair, then the model accurately maintained two unique compartments.
One nonintuitive aspect of the model is that it predicts that both members of a SNARE pair, the v- and t-SNAREs, accumulate in the target compartment, a prediction borne out by experimental observations from other groups.
COPII is known to have high affinity for SNAREs that target the Golgi, and the model predicts that COPI should preferentially bind to ER SNAREs. If, however, the coat protein's binding affinity for a SNARE pair is too strong, then all of those SNARE proteins would accumulate in the target compartment, leaving vesicles to bud from the other compartment without any SNAREs that would allow it to fuse to the target membrane. The model also predicts that if one SNARE pair is overexpressed, then the size of its target compartment would increase.
Rbiya S. Tuma
rabiya@nasw.org
Reinhart Heinrich and Tom A. Rapoport
J. Cell Biol. 2005 168: 271-280.(Differential affinities between coats an)