GroEL/ES Buffering and Compensatory Mutations Promote Protein Evolution by Stabilizing Folding Intermediates

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• 作者：Kirsten T. Wyganowski ; Miriam Kaltenbach ; Nobuhiko Tokuriki
• 关键词：PTE ; phosphotriesterase ; 2NH ; 2-naphthyl hexanoate ; bis-ANS ; 4 ; 4&prime ; -bis(1-anilinonaphthalene 8-sulfonate) ; GdnHCl ; guanidine hydrochloride ; amp ; ampicillin ; cam ; chloramphenicol
• 刊名：Journal of Molecular Biology
• 出版年：2013
• 出版时间：23 September, 2013
• 年：2013
• 卷：425
• 期：18
• 页码：3403-3414
• 全文大小：979 K

文摘

Maintaining stability is a major constraint in protein evolution because most mutations are destabilizing. Buffering and/or compensatory mechanisms that counteract this progressive destabilization during functional adaptation are pivotal for protein evolution as well as protein engineering. However, the interplay of these two mechanisms during a full evolutionary trajectory has never been explored. Here, we unravel such dynamics during the laboratory evolution of a phosphotriesterase into an arylesterase. A controllable GroEL/ES chaperone co-expression system enabled us to vary the selection environment between buffering and compensatory, which smoothened the trajectory along the fitness landscape to achieve a > 10⁴ increase in arylesterase activity. Biophysical characterization revealed that, in contrast to prevalent models of protein stability and evolution, the variants' soluble cellular expression did not correlate with in vitro stability, and compensatory mutations were linked to a stabilization of folding intermediates. Thus, folding kinetics in the cell are a key feature of protein evolvability.