Literature DB >> 20133683

Capillarity theory for the fly-casting mechanism.

Emmanuel Trizac1, Yaakov Levy, Peter G Wolynes.   

Abstract

Biomolecular folding and function are often coupled. During molecular recognition events, one of the binding partners may transiently or partially unfold, allowing more rapid access to a binding site. We describe a simple model for this fly-casting mechanism based on the capillarity approximation and polymer chain statistics. The model shows that fly casting is most effective when the protein unfolding barrier is small and the part of the chain which extends toward the target is relatively rigid. These features are often seen in known examples of fly casting in protein-DNA binding. Simulations of protein-DNA binding based on well-funneled native-topology models with electrostatic forces confirm the trends of the analytical theory.

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Year:  2010        PMID: 20133683      PMCID: PMC2840330          DOI: 10.1073/pnas.0914727107

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  35 in total

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4.  Fly-casting in protein-DNA binding: frustration between protein folding and electrostatics facilitates target recognition.

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  38 in total

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Journal:  J Mol Biol       Date:  2018-06-05       Impact factor: 5.469

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