The mechanism of papain inhibition by peptidyl aldehydes

Michael Shokhen, Netaly Khazanov, Amnon Albeck

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Various mechanisms for the reversible formation of a covalent tetrahedral complex (TC) between papain and peptidyl aldehyde inhibitors were simulated by DFT calculations, applying the quantum mechanical/self consistent reaction field (virtual solvent) [QM/SCRF(VS)] approach. Only one mechanism correlates with the experimental kinetic data. The His-Cys catalytic diad is in an N/SH protonation state in the noncovalent papain-aldehyde Michaelis complex. His159 functions as a general base catalyst, abstracting a proton from the Cys25, whereas the activated thiolate synchronously attacks the inhibitor's carbonyl group. The final product of papain inhibition is the protonated neutral form of the hemithioacetal TC(OH), in agreement with experimental data. The predicted activation barrier genz≠ = 5.2 kcal mol -1 is close to the experimental value of 6.9 kcal mol -1. An interpretation of the experimentally observed slow binding effect for peptidyl aldehyde inhibitors is presented. The calculated gcat≠ is much lower than the rate determining activation barrier of hemithioacetal formation in water, gw≠, in agreement with the concept that the preorganized electrostatic environment in the enzyme active site is the driving force of enzyme catalysis. We have rationalized the origin of the acidic and basic pK a's on the k 2/K S versus pH bell-shaped profile of papain inhibition by peptidyl aldehydes.

Original languageEnglish
Pages (from-to)975-985
Number of pages11
JournalProteins: Structure, Function and Bioinformatics
Volume79
Issue number3
DOIs
StatePublished - Mar 2011

Keywords

  • Enzyme mechanism
  • Molecular modelling
  • PK in proteins
  • Papain
  • Quantum mechanics
  • Solvation

Fingerprint

Dive into the research topics of 'The mechanism of papain inhibition by peptidyl aldehydes'. Together they form a unique fingerprint.

Cite this