Analysis of RNase A refolding intermediates by electrospray/mass spectrometry

FEBS Lett. 1994 Oct 3;352(3):301-6. doi: 10.1016/0014-5793(94)00966-x.

Abstract

Electrospray/mass spectrometry (ES/MS) was extensively used to obtain information on disulphide-containing intermediates formed during refolding of bovine pancreatic ribonuclease A. The analysis showed the existence of an equilibrated population of disulphide bonded intermediates, and indicates that intermediates containing two intramolecular S-S are predominant until late stages of the refolding process. Mixed disulphides with exogenous glutathione were also detected, supporting previous evidence of conformational restrictions on the ability of RNase A to form intramolecular disulphides. The results indicate that ES/MS is a suitable technique to detect and characterize refolding intermediates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Guanidine
  • Guanidines
  • Kinetics
  • Mass Spectrometry
  • Pancreas / enzymology
  • Protein Denaturation
  • Protein Folding*
  • Ribonuclease, Pancreatic / chemistry*
  • Ribonuclease, Pancreatic / metabolism
  • Sulfhydryl Compounds
  • Sulfhydryl Reagents
  • Time Factors
  • Urea

Substances

  • Guanidines
  • Sulfhydryl Compounds
  • Sulfhydryl Reagents
  • Urea
  • Ribonuclease, Pancreatic
  • Guanidine