Theory of the Kinetics of Conformational Transitions in Polymers

1971 ◽  
Vol 54 (11) ◽  
pp. 4651-4661 ◽  
Author(s):  
Eugene Helfand
Polymer ◽  
2010 ◽  
Vol 51 (11) ◽  
pp. 2410-2416 ◽  
Author(s):  
Kun Tian ◽  
David Porter ◽  
Jinrong Yao ◽  
Zhengzhong Shao ◽  
Xin Chen

Biochemistry ◽  
2006 ◽  
Vol 45 (5) ◽  
pp. 1435-1441 ◽  
Author(s):  
Ken Solt ◽  
Jonas S. Johansson ◽  
Douglas E. Raines

1985 ◽  
Vol 43 (2) ◽  
pp. 891-895
Author(s):  
P. M. Pakhomov ◽  
I. I. Novak ◽  
M. V. Shablygin ◽  
V. E. Korsukov

1980 ◽  
Vol 72 (10) ◽  
pp. 5489-5500 ◽  
Author(s):  
Jeffrey Skolnick ◽  
Eugene Helfand

1985 ◽  
Vol 63 (6) ◽  
pp. 693-703
Author(s):  
James G. Foulks ◽  
Lillian Morishita

D2O and perchlorate manifest opposing effects on the contractile function of skeletal muscle (amplitude of twitches and maximum K contractures, potential dependence of contraction activation and inactivation), and when combined the influence of one may effectively antagonize that of the other. The ratio of perchlorate concentrations required to produce effects of equal intensity (e.g., twitch enhancement and restoration of maximum K contractures in media lacking divalent cations or containing a depressant concentration of a cationic amphipath) in H2O and D2O solutions was generally rather constant. These findings are compatible with the view that both agents can influence contractile function by virtue of their effects on solvent structure. In the absence of divalent cations, the effects of reduced temperature resemble those of D2O whereas the effects of increased temperature resemble those of the chaotropic anion. However, in other media, variation in temperature was found to result in additional nonsolvent effects so that low temperature could oppose rather than enhance the effects of D2O. These observations are discussed in terms of a model which postulates a role for solvent influences on the kinetics of two separate potential-dependent conformational transitions of membrane proteins which mediate the activation and inactivation of contraction in skeletal muscle.


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