TY - JOUR
T1 - Downhill dynamics and the molecular rate of protein folding
AU - Liu, Feng
AU - Gruebele, Martin
N1 - Funding Information:
This work was supported by grant MCB 0613643 of the National Science Foundation, and by a William and Janet Lycan Professorship.
PY - 2008/8/8
Y1 - 2008/8/8
N2 - Proteins are held together by many weak contacts, each corresponding to a local reaction coordinate. The activation barrier for folding is distributed along a resultant global folding coordinate. Hence folding barriers are low, and could even become comparable to the thermal energy kT. In that case, proteins become downhill folders, with folding times in the microsecond region. Small barriers allow the diffusion of population along the reaction coordinate - the molecular rate - to be observed directly. Five simple free energy building blocks can explain all experimentally observed fast folding data, revealing a range of behaviors from low barrier crossings to completely downhill folding.
AB - Proteins are held together by many weak contacts, each corresponding to a local reaction coordinate. The activation barrier for folding is distributed along a resultant global folding coordinate. Hence folding barriers are low, and could even become comparable to the thermal energy kT. In that case, proteins become downhill folders, with folding times in the microsecond region. Small barriers allow the diffusion of population along the reaction coordinate - the molecular rate - to be observed directly. Five simple free energy building blocks can explain all experimentally observed fast folding data, revealing a range of behaviors from low barrier crossings to completely downhill folding.
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U2 - 10.1016/j.cplett.2008.04.075
DO - 10.1016/j.cplett.2008.04.075
M3 - Article
AN - SCOPUS:48149114503
SN - 0009-2614
VL - 461
SP - 1
EP - 8
JO - Chemical Physics Letters
JF - Chemical Physics Letters
IS - 1-3
ER -