Isolation of sarcoplasmic reticulum by zonal centrifugation and purification of Ca2+-pump and Ca2+-binding proteins

Gerhard Meissner, Gregory E Conner, Sidney Fleischer

Research output: Contribution to journalArticle

313 Citations (Scopus)

Abstract

A procedure for the isolation of highly purified sarcoplasmic reticulum vesicles from rabbit skeletal muscle has been described using sucrose gradient centrifugation in zonal rotors. The yield of our purest fraction was 300 mg of sarcoplasmic reticulum protein using 1 kg muscle. The sarcoplasmic reticulum vesicles were relatively simple in composition. The Ca2+-pump protein accounted for most (approx. two-thirds) of the sarcoplasmic reticulum protein. Two other protein components, a Ca2+-binding protein and a M55 protein (approx. 55 000 daltons) each accounted for about 5-10% of the protein. Enrichment in the level of phosphoenzyme by the Ca2+-pump protein was regarded as an important index of the purification of sarcoplasmic reticulum vesicles. The sarcoplasmic reticulum vesicles were capable of forming 6.4 nmoles of 32P-labelled phosphoenzyme per mg protein and had a high capacity of energized Ca2+ uptake. The Ca2+-dependent formation of phosphoenzyme has been used to estimate the sarcoplasmic reticulum protein content in rabbit skeletal muscle and found to be about 2.5% of the total muscle protein. The Ca2+-pump and Ca2+-binding proteins were isolated with a purity of 90% or more by treating the purified sarcoplasmic reticulum vesicles with bile acids in the presence of salt. The solubilized Ca2+-pump protein reaggregated during dialysis together with phospholipid to form membranous vesicles which were capable of forming approx. 9 nmoles 32P-labelled phosphoenzyme per mg protein. The Ca2+-binding protein was water soluble and contained a high percentage of acidic amino acids (35% of total residues). Ca2+ binding by sarcoplasmic reticulum vesicles and by the Ca2+-pump and Ca2+-binding proteins was studied by equilibrium dialysis. Sarcoplasmic reticulum vesicles and Ca2+-pump protein contained nonspecific high-affinity Ca2+ binding sites with a capacity of 90-100 and 55-70 nmoles Ca2+ per mg protein, respectively. Both of them specifically bound 10-15 nmoles Ca2+ per mg protein. The binding constants for nonspecific and specific Ca2+ binding by both preparations were approx. 1 μM-1. The Ca2+-binding protein nonspecifically bound 900-1000 nmoles Ca2+ per mg protein with a binding constant of about 0.25 μM-1.

Original languageEnglish
Pages (from-to)246-269
Number of pages24
JournalBBA - Biomembranes
Volume298
Issue number2
DOIs
StatePublished - Mar 16 1973
Externally publishedYes

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Zonal Centrifugation
Centrifugation
Sarcoplasmic Reticulum
Purification
Carrier Proteins
Pumps
Proteins
Muscle
Dialysis
Skeletal Muscle
Rabbits
Acidic Amino Acids
Muscle Proteins

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Cell Biology
  • Medicine(all)

Cite this

Isolation of sarcoplasmic reticulum by zonal centrifugation and purification of Ca2+-pump and Ca2+-binding proteins. / Meissner, Gerhard; Conner, Gregory E; Fleischer, Sidney.

In: BBA - Biomembranes, Vol. 298, No. 2, 16.03.1973, p. 246-269.

Research output: Contribution to journalArticle

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