Quest for a turnover mechanism in peptide-based enzyme mimics

Tsukasa Takahashi, Michelle Cheung, Thomas Butterweck, Steve Schankweiler, Michael (Mike) Heller

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Creation of synthetic structures with an enzyme-like mechanism and turnover remains a significant challenge. In this study, peptides containing a cysteine thiol and histidine imidazole group were designed to mimic the active site of the cysteine protease papain. Ellman's reagent trapping experiments showed that rapid acetyl group exchange exists between the thiol and imidazole groups. This exchange rate increased significantly in peptides with bulky R-groups (phenylalanine) between the cysteine and histidine. A reduction of the cysteine thiol pKa and NMR results further supports closer proximity of the thiol and imidazole groups in peptides with faster acetyl group exchange.

Original languageEnglish (US)
Pages (from-to)206-210
Number of pages5
JournalCatalysis Communications
Volume59
DOIs
StatePublished - Jan 10 2015
Externally publishedYes

Fingerprint

Sulfhydryl Compounds
Peptides
Enzymes
Cysteine
Histidine
Papain
Dithionitrobenzoic Acid
Cysteine Proteases
Phenylalanine
Nuclear magnetic resonance
Experiments
imidazole

Keywords

  • Enzyme mimics
  • Papain Proteases
  • Synthetic peptides
  • Synzymes

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Process Chemistry and Technology

Cite this

Quest for a turnover mechanism in peptide-based enzyme mimics. / Takahashi, Tsukasa; Cheung, Michelle; Butterweck, Thomas; Schankweiler, Steve; Heller, Michael (Mike).

In: Catalysis Communications, Vol. 59, 10.01.2015, p. 206-210.

Research output: Contribution to journalArticle

Takahashi, Tsukasa ; Cheung, Michelle ; Butterweck, Thomas ; Schankweiler, Steve ; Heller, Michael (Mike). / Quest for a turnover mechanism in peptide-based enzyme mimics. In: Catalysis Communications. 2015 ; Vol. 59. pp. 206-210.
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