Binding takes cooperation
http://www.100md.com
《细胞学杂志》
Klein/Elsevier
The CDK inhibitor Sic1 gets proteolyzed in late G1, but the regulation of its binding to the Cdc4 ubiquitin ligase subunit has been a conundrum. The proteins do not bind unless Sic1 is phosphorylated on at least six of its nine sites, yet Cdc4 can harbor only one phosphorylated epitope. Traditional thermodynamic arguments cannot explain this puzzle, but a new mathematical model from Peter Klein (Fox Run Management, Greenwich, CT), Tony Pawson, and Mike Tyers (University of Toronto, Toronto, Canada) offers an explanation.
The group imagined that additional binding sites might make Sic1 more likely to rebind at another site than to diffuse away from Cdc4. "It's like seaweed floating in the waves," says Klein. "Pieces get stuck on a rock. A wave might knock it off, but before it floats away, another arm can get stuck." Their model shows that the affinity of Cdc4 for Sic1 grows exponentially with each Sic1 phosphorylation, an effect they call allovalency. As long as diffusion is sufficiently slow and rebinding is rapid enough, the model is possible kinetically when biophysically realistic numbers are considered.
Extension of this model is possibly limited by the critical assumption that each binding site must be able to move independently, as is the case for the unstructured Sic1. Lectins and their long-chain carbohydrate ligands might also fit this sort of model.
Reference:
Klein, P., et al. 2003. Curr. Biol. 13:1669–1678.(The odds of binding rise rapidly with mo)
The CDK inhibitor Sic1 gets proteolyzed in late G1, but the regulation of its binding to the Cdc4 ubiquitin ligase subunit has been a conundrum. The proteins do not bind unless Sic1 is phosphorylated on at least six of its nine sites, yet Cdc4 can harbor only one phosphorylated epitope. Traditional thermodynamic arguments cannot explain this puzzle, but a new mathematical model from Peter Klein (Fox Run Management, Greenwich, CT), Tony Pawson, and Mike Tyers (University of Toronto, Toronto, Canada) offers an explanation.
The group imagined that additional binding sites might make Sic1 more likely to rebind at another site than to diffuse away from Cdc4. "It's like seaweed floating in the waves," says Klein. "Pieces get stuck on a rock. A wave might knock it off, but before it floats away, another arm can get stuck." Their model shows that the affinity of Cdc4 for Sic1 grows exponentially with each Sic1 phosphorylation, an effect they call allovalency. As long as diffusion is sufficiently slow and rebinding is rapid enough, the model is possible kinetically when biophysically realistic numbers are considered.
Extension of this model is possibly limited by the critical assumption that each binding site must be able to move independently, as is the case for the unstructured Sic1. Lectins and their long-chain carbohydrate ligands might also fit this sort of model.
Reference:
Klein, P., et al. 2003. Curr. Biol. 13:1669–1678.(The odds of binding rise rapidly with mo)