The Alkali Molten Globule State of Horse Ferricytochrome c: Observation of Cold Denaturation

dc.contributor.author Kumar, Rajesh
dc.contributor.author Prabhu, N. Prakash
dc.contributor.author Rao, D. Krishna
dc.contributor.author Bhuyan, Abani K.
dc.date.accessioned 2022-03-27T05:18:53Z
dc.date.available 2022-03-27T05:18:53Z
dc.date.issued 2006-12-01
dc.description.abstract Here, we present the basic structural properties and the thermodynamic description of a previously unknown alkali molten globule state of horse "ferricytochrome c". Both sodium and guanidinium cations stabilize the alkali-denatured state at pH 13, presumably by a charge screening mechanism. The Na+-stabilized conformation (B state) clearly meets with the molecular organizational definition of the generic molten globule state. The B state exhibits highly cooperative thermal unfolding transitions monitored by both near and far-UV CD. Analyses of these transitions show substantial heat capacity change, suggesting that the hydrophobic effect contributes considerably to its energetic stability. At low salt concentration where molten globules are less stable, the B state undergoes reversible cold denaturation. © 2006 Elsevier Ltd. All rights reserved.
dc.identifier.citation Journal of Molecular Biology. v.364(3)
dc.identifier.issn 00222836
dc.identifier.uri 10.1016/j.jmb.2006.09.025
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0022283606012162
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/8016
dc.subject B state
dc.subject cold denaturation
dc.subject cytochrome c
dc.subject molten globule
dc.subject protein folding
dc.title The Alkali Molten Globule State of Horse Ferricytochrome c: Observation of Cold Denaturation
dc.type Journal. Article
dspace.entity.type
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