PEGylated substrates of NSP4 protease: A tool to study protease specificity

نویسندگان

  • Magdalena Wysocka
  • Natalia Gruba
  • Renata Grzywa
  • Artur Giełdoń
  • Remigiusz Bąchor
  • Krzysztof Brzozowski
  • Marcin Sieńczyk
  • Jenne Dieter
  • Zbigniew Szewczuk
  • Krzysztof Rolka
  • Adam Lesner
چکیده

Herein we present the synthesis of a novel type of peptidomimetics composed of repeating diaminopropionic acid residues modified with structurally diverse heterobifunctional polyethylene glycol chains (abbreviated as DAPEG). Based on the developed compounds, a library of fluorogenic substrates was synthesized. Further library deconvolution towards human neutrophil serine protease 4 (NSP4) yielded highly sensitive and selective internally quenched peptidomimetic substrates. In silico analysis of the obtained peptidomimetics revealed the presence of an interaction network with distant subsites located on the enzyme surface.

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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2016