Exploiting the right side of the Ramachandran plot: substitution of glycines by D-alanine can significantly increase protein stability |
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Authors: | Anil Burcu Song Benben Tang Yuefeng Raleigh Daniel P |
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Affiliation: | Department of Chemistry, State University of New York at Stony Brook, Stony Brook, New York 11794, USA. |
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Abstract: | A major goal of protein engineering is the enhancement of protein stability. Here we demonstrate a rational method for enhancing the stability of globular proteins by targeting glycine residues which adopt conformations with Phi > 0. Replacement of such a glycine by d-alanine can lead to a significant increase in stability. The approach is tested at three sites in two model proteins. NMR and CD indicated that the substitutions do not alter the structure. Replacement of glycine-24 of the N-terminal domain of L9 (NTL9) with d-Ala results in an increase in stability of 1.3 kcal mol-1, while replacement of glycine-34 of NTL9 leads to an increase of 1.9 kcal mol-1. Replacement of glycine-331 of the UBA domain with d-Ala leads to an increase in stability of 0.6 kcal mol-1. |
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