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Article
"Click" reactions: a versatile toolbox for the synthesis of peptide-conjugates
Chemical Society Reviews
  • Wen Tang, University of Akron Main Campus
  • Matthew Becker, University of Akron
Document Type
Article
Publication Date
10-24-2014
Abstract

Peptides that comprise the functional subunits of proteins have been conjugated to versatile materials (biomolecules, polymers, surfaces and nanoparticles) in an effort to modulate cell responses, specific binding affinity and/or self-assembly behavior. However, the efficient and convenient synthesis of peptide-conjugates, especially the constructs with multiple types of peptide functionality remains challenging. In this critical review, we focus on "click" reactions that have been used to synthesis peptide-functionalized conjugates, introducing their reaction conditions, specifically elucidating parameters that influence reaction kinetics and total conversion, and highlighting examples that have been completed recently. Moreover, orthogonal "click" reactions that synthesize multi-functional biomaterials in a one-pot or sequential manner are noted. Through this review, a comprehensive understanding of "click" reactions aims to provide insight on how one might choose suitable "click" reactions to constitute peptide-functionalized molecules/surfaces/matrices for the development of advanced biomaterials.

Citation Information
Wen Tang and Matthew Becker. ""Click" reactions: a versatile toolbox for the synthesis of peptide-conjugates" Chemical Society Reviews Vol. 43 Iss. 20 (2014) p. 7013 - 7039
Available at: http://works.bepress.com/matthew_becker/95/