Specific fluorescent derivatives of macromolecules. Reaction of dansyl fluoride with serine proteinases

Biochim Biophys Acta. 1976 Jul 19;439(1):194-205. doi: 10.1016/0005-2795(76)90175-6.

Abstract

5-Dimethylaminonaphthalene-1-sulfonyl fluoride was evaluated as a reagent for the selective labeling of proteins. In a comparative study with Dns-chloride a greatly increased selectivity of the fluoride was found with a number of proteins. The reaction of Dns-fluoride with alpha-chymotrypsin, subtilisin Carlsberg and trypsin was found to be highly specific, resulting in a stoichiometric incorporation of the Dns label with concomitant loss of enzymatic activity. The reaction of Dns-chloride with the same proteinases is unspecific. Evidence was obtained to indicate that reaction of the serine esterases with Dns-fluoride occurs exclusively at the active serine residue. The stability of Dns-fluoride labeled chymotrypsin was investigated. The conjugate was found to be fairly stable in the pH range from 3 to 9 at 25 degrees C and is therefore suitable for fluorescence investigations of the chymotrypsin active-site. Molar extinction coefficients for Dns-labeled serine proteinases were determined using radiocative label.

MeSH terms

  • Binding Sites
  • Chlorides
  • Dansyl Compounds
  • Endopeptidases* / metabolism
  • Fluorides
  • Hydrogen-Ion Concentration
  • Kinetics
  • Protein Binding
  • Protein Conformation
  • Serine
  • Spectrometry, Fluorescence

Substances

  • Chlorides
  • Dansyl Compounds
  • Serine
  • Endopeptidases
  • Fluorides