4.7 Article

Polymerization of a peptide-based enzyme substrate

期刊

CHEMICAL COMMUNICATIONS
卷 49, 期 28, 页码 2873-2875

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc40472b

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资金

  1. NIH T32 [5T32EB005970]
  2. Dept. of Radiology
  3. AFOSR-PECASE [FA9550-11-1-0105]
  4. ARO [W911NF-11-1-0264]
  5. NIH [NIBIB 1R01EB011633]
  6. NIH Transformative Research Award [R01HL117326]
  7. NIH Director's New Innovator Award [1DP2OD008724]
  8. Henry & Camille Dreyfus Foundation

向作者/读者索取更多资源

Polymers of norbornenyl-modified peptide-based enzyme substrates have been prepared via ring-opening metathesis polymerization (ROMP). Peptides displayed on water-soluble homopolymers retain the ability to be enzymatically processed by a disease-associated enzyme. In contrast, when the peptides are densely arrayed on a nanoparticle derived from a self-assembled amphiphilic block-copolymer, they function with reduced activity as enzymatic substrates.

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