Purification of putative Ca2+ channel protein from rabbit skeletal muscle. Determination of the amino-terminal sequence

J Biol Chem. 1987 May 15;262(14):6572-6.

Abstract

A putative Ca2+ channel protein was purified from rabbit skeletal muscle transverse tubules with the combined use of lectin affinity chromatography and ion-exchange chromatography, followed by sucrose density gradient centrifugation. The major component of the purified preparation detected by sodium dodecyl sulfate-gel electrophoresis was a protein of 150 kDa when reduced with 20 mM dithiothreitol and a 191-kDa protein when treated with 20 mM N-ethylmaleimide. Therefore, this protein appears to be identical with the alpha subunit previously described (Curtis, B. M., and Catterall, W. A. (1984) Biochemistry 23, 2113-2118). This protein was purified by preparative sodium dodecyl sulfate-gel electrophoresis, followed by electroelution and/or electroblotting, and its amino acid composition and NH2-terminal sequence were determined. The NH2-terminal sequence is: NH2-Glu-Pro-Phe-Pro-Ser-Ala-Val-X-Ile-Lys-Ser-X-Val-X-Lys-Met-Gln-.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Calcium / metabolism*
  • Calcium Channels
  • Ion Channels / metabolism*
  • Membrane Proteins / isolation & purification
  • Molecular Weight
  • Muscle Proteins / isolation & purification*
  • Muscles / metabolism*
  • Rabbits
  • Receptors, Nicotinic / isolation & purification*
  • Solubility

Substances

  • Calcium Channels
  • Ion Channels
  • Membrane Proteins
  • Muscle Proteins
  • Receptors, Nicotinic
  • Calcium