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Synthesis and folding of a mirror-image enzyme reveals ambidextrous chaperone activity.


ABSTRACT: Mirror-image proteins (composed of D-amino acids) are promising therapeutic agents and drug discovery tools, but as synthesis of larger D-proteins becomes feasible, a major anticipated challenge is the folding of these proteins into their active conformations. In vivo, many large and/or complex proteins require chaperones like GroEL/ES to prevent misfolding and produce functional protein. The ability of chaperones to fold D-proteins is unknown. Here we examine the ability of GroEL/ES to fold a synthetic d-protein. We report the total chemical synthesis of a 312-residue GroEL/ES-dependent protein, DapA, in both L- and D-chiralities, the longest fully synthetic proteins yet reported. Impressively, GroEL/ES folds both L- and D-DapA. This work extends the limits of chemical protein synthesis, reveals ambidextrous GroEL/ES folding activity, and provides a valuable tool to fold d-proteins for drug development and mirror-image synthetic biology applications.

SUBMITTER: Weinstock MT 

PROVIDER: S-EPMC4136631 | biostudies-literature | 2014 Aug

REPOSITORIES: biostudies-literature

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Synthesis and folding of a mirror-image enzyme reveals ambidextrous chaperone activity.

Weinstock Matthew T MT   Jacobsen Michael T MT   Kay Michael S MS  

Proceedings of the National Academy of Sciences of the United States of America 20140728 32


Mirror-image proteins (composed of D-amino acids) are promising therapeutic agents and drug discovery tools, but as synthesis of larger D-proteins becomes feasible, a major anticipated challenge is the folding of these proteins into their active conformations. In vivo, many large and/or complex proteins require chaperones like GroEL/ES to prevent misfolding and produce functional protein. The ability of chaperones to fold D-proteins is unknown. Here we examine the ability of GroEL/ES to fold a s  ...[more]

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