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March 20, 2015Journal of the American Chemical Society192 citationsOpen Access

Peptide/Protein Stapling and Unstapling: Introduction of s -Tetrazine, Photochemical Release, and Regeneration of the Peptide/Protein

SBStephen P. BrownASAmos B. Smith

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Abstract

Protocols have been achieved that permit facile introduction of s-tetrazine into unprotected peptides and the protein, thioredoxin, between two cysteine sulfhydryl groups (i.e., staple), followed by photochemical release (i.e., unstaple) and regeneration of the peptide/protein upon removal of the cyano groups from the derived bisthiocyanate. The S,S-tetrazine macrocycles in turn provide a convenient handle for probe introduction by exploiting the inverse electron demand Diels-Alder reactivity of the tetrazine.

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Cite This Study

Brown et al. (2015) studied this question.

synapsesocial.com/papers/6a1279121292a1e50c350237https://doi.org/10.1021/ja512880g
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