Title of article :
Kinetics of breaking a salt-bridge critical in protein unfolding
Author/Authors :
Gruia، نويسنده , , Andreea D. and Fischer، نويسنده , , Stefan Bo Smith، نويسنده , , Jeremy C.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
4
From page :
337
To page :
340
Abstract :
The rate of breaking an Arg–Glu salt bridge on the surface of a globular protein (Staphylococcal nuclease) is determined by using molecular dynamics simulations to derive the free energy activation barrier to dissociation and the pre-exponential rate factor for that reaction. The dissociation barrier obtained is 7 kcal/mol. The pre-exponential factor is derived using a novel method in which simulations are performed for the same system with the salt bridge weakened such that the rate can be observed directly. Combining the prefactor thus obtained (5×1011 s−1) with the above dissociation barrier height yields an estimated lifetime of the salt-bridge of 200 ns, suggesting that surface salt-bridges can cause significant kinetic barriers to protein folding or unfolding.
Journal title :
Chemical Physics Letters
Serial Year :
2004
Journal title :
Chemical Physics Letters
Record number :
1783087
Link To Document :
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