Proceedings of the National Academy of Sciences · 1989 · 94 citations · 30 references
Life SciencesBiochemistryMolecular BiologyCellular BiochemistryMetabolic StabilityProtein EngineeringEnzyme StabilityThermostability EngineeringDirected MutagenesisPositionProtein Engineering For ThermostabilityProtein Thermal AdaptationThermostabilityThermostability Mechanisms
Two Saccharomyces cerevisiae yeast mutants, cyc1-73 and cyc1-190, contain nonfunctional and presumably unstable forms of iso-1-cytochrome c due to Gly-34----Ser and His-38----Pro replacements, respectively. Second-site reversions that produced Asn-57----Ile replacements at least partially restored function, presumably by alleviating the instability of these two altered iso-1-cytochromes c. Introduction of the Ile-57 replacement by site-directed mutagenesis in an otherwise normal protein resulted in a 17 degrees C increase in the transition temperature (Tm), corresponding to over a 2-fold increase in the free energy change (delta G degrees) for thermal unfolding.
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Prediction of protein conformation
Peter Y. Chou, Gerald D. Fasman · Biochemistry · 1974 · 3.3K citations