4.8 Article

Redox-Switchable Surface for Controlling Peptide Structure

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 133, Issue 23, Pages 8870-8873

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja203198y

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Funding

  1. Carolina Center for Cancer Nanotechnology Excellence (National Cancer Institute)
  2. NSF
  3. Burroughs Wellcome Foundation

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A general surface chemistry strategy is described for the development of a new switchable material. The method modulates a surface-immobilized-molecules structure by using two orthogonal click reactions based on Huisgen cycloaddition and oxime chemistry, where the oxime linkage is redox active and switchable. We demonstrate this strategy by developing a noninvasive, biocompatible, in situ surface chemistry that is able to modulate the affinity of a cell-adhesive peptide to cell integrin receptors to study dynamic cell adhesion and cell migration in real time and as a new hide-and-reveal strategy for application in new types of smart biofouling biomaterials.

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