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Fast Folding of a Helical Protein Initiated by the Collision of Unstructured Chains
W. Kevin Meisner, Tobin R. Sosnick and Michael Levitt
Proceedings of the National Academy of Sciences of the United States of America
Vol. 101, No. 37 (Sep. 14, 2004), pp. 13478-13482
Published by: National Academy of Sciences
Stable URL: http://www.jstor.org/stable/3373336
Page Count: 5
You can always find the topics here!Topics: Biochemistry, Hydrogen bonds, Kinetics, Modeling, pH, Solvents, Monomers, Molecular chains, Sodium, Free energy
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To examine whether helix formation necessarily precedes chain collision, we have measured the folding of a fully helical coiled coil that has been specially engineered to have negligible intrinsic helical propensity but high overall stability. The folding rate approaches the diffusion-limited value and is much faster than possible if folding is contingent on precollision helix formation. Therefore, the collision of two unstructured chains is the initial step of the dominant kinetic pathway, whereas helicity exerts its influence only at a later step. Folding from an unstructured encounter complex may be efficient and robust, which has implications for any biological process that couples folding to binding.
Proceedings of the National Academy of Sciences of the United States of America © 2004 National Academy of Sciences