Porphyrinmaleimides: towards thiol probes for cysteine residues in proteins

Bioconjug Chem. 2008 Jan;19(1):5-9. doi: 10.1021/bc700267f. Epub 2007 Dec 8.

Abstract

Porphyrinmaleimides were synthesized and characterized. The thiol-containing amino acid L-cysteine reacted with 58% yield with these porphyrins to form bioconjugate adducts. The new thiol-active reagents were labeled cytoplasmic cysteine 140 and 316 in rhodopsin (Rh), a G protein coupled receptor (GPCR).

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cysteine / analysis*
  • Cysteine / chemistry*
  • Electrophoresis, Polyacrylamide Gel
  • Light
  • Maleimides / chemical synthesis*
  • Maleimides / chemistry*
  • Porphyrins / chemistry*
  • Rhodopsin / chemistry*
  • Sulfhydryl Compounds / chemistry*
  • Ultraviolet Rays

Substances

  • Maleimides
  • Porphyrins
  • Sulfhydryl Compounds
  • maleimide
  • Rhodopsin
  • Cysteine