Open Access. Powered by Scholars. Published by Universities.®
Physical Sciences and Mathematics Commons™
Open Access. Powered by Scholars. Published by Universities.®
Articles 1 - 2 of 2
Full-Text Articles in Physical Sciences and Mathematics
Folding Under Inequilibrium Conditions As A Possible Reason For Partial Irreversibility Of Heat-Denatured Proteins: Computer Simulation Study, Sergey A. Potekhin, Evgueni Kovriguine
Folding Under Inequilibrium Conditions As A Possible Reason For Partial Irreversibility Of Heat-Denatured Proteins: Computer Simulation Study, Sergey A. Potekhin, Evgueni Kovriguine
Chemistry Faculty Research and Publications
Using computer simulations we have studied possible effects of heating and cooling at different scan rates on unfolding and refolding of macromolecules. We have shown that even the simplest two-state reversible transition can behave irreversibly when an unfavorable combination of cooling rate, relaxation time and activation energy of refolding occurs. On the basis of this finding we suppose that apparent irreversibility of some proteins denatured by heat may result from slow relaxation on cooling rather than thermodynamic instability and/or irreversible alterations of the polypeptide chain. Using this kinetic reversible two-state model, we estimated the effects of the scan rate and …
A Kinetic Study Of The Photolysis Of Ethylferrocene In Chloroform, Son L. Phan, Patrick E. Hoggard
A Kinetic Study Of The Photolysis Of Ethylferrocene In Chloroform, Son L. Phan, Patrick E. Hoggard
Chemistry and Biochemistry
The photooxidation of ethylferrocene to ethylferricinium ion and tetrachloroferrate in CHCl3 under 254 nm irradiation proceeds through light absorption by both ethylferrocene and chloroform. The products remain in solution at concentrations below 10-3 M. The fraction occurring through a solvent-initiated pathway increases during the course of the reaction. A secondary thermal reaction is responsible for generating tetrachloroferrate from ethylferricinium ion. The rate of the reaction increases during the early stages, and the data throughout the course of the reaction are consistent with the rate law ( afs + bfR)/ (1 + c[R]/[P]-d[R]/[Cl ]), where [R] and [P] are the concentrations …