Relationships among the subunits of the high molecular weight proteinase, macropain (proteasome)

Lawrence W. Lee, Carolyn R. Moomaw, Kim Orth, Michael J. McGuire, George N. DeMartino, Clive A. Slaughter

Research output: Contribution to journalArticle

56 Citations (Scopus)

Abstract

An analysis of the subunits of the high molecular weight proteinase, macropain (multicatalytic proteinase or proteasome) from human erythrocytes has been conducted using N-terminal amino acid sequencing, gel electrophoresis and reverse-phase peptide mapping. This analysis provided evidence for the existence of 13 subunits of different primary structure. Five subunits were susceptible to the Edman degradation and yielded unique N-terminal sequences. Similarities among these sequences, however, indicated that the subunits are homologues. Two-dimensional gel electrophoresis discriminated 10 major components, which included two of the subunits for which N-terminal sequences had been determined and eight N-terminally blocked subunits. Tryptic peptide mapping indicated that all 10 of these components have a different amino acid sequence. Tryptic peptides from some of the subunits were subjected to amino acid sequence analysis, and the data indicated that all the subunits tested in this way are related by common ancestry. The data suggest that at least nine of the total of 13 subunits are encoded by members of the same gene family; the remaining four subunits have not yet been investigated in sufficient detail to establish their relationships. No evidence for a close relationship with any previously investigated proteinase family has been found. Finally, through a comparison of the 'latent' and 'active' forms of macropain, the study established a close similarity in the subunit composition of these catalytically very different species, although proteolytic degradation of selected subunits appears in the active form of the enzyme.

Original languageEnglish (US)
Pages (from-to)178-185
Number of pages8
JournalBiochimica et Biophysica Acta (BBA)/Protein Structure and Molecular
Volume1037
Issue number2
DOIs
StatePublished - Feb 9 1990
Externally publishedYes

Fingerprint

Proteasome Endopeptidase Complex
Peptide Hydrolases
Molecular Weight
Molecular weight
Peptide Mapping
Protein Sequence Analysis
Electrophoresis
Amino Acids
Peptides
Gels
Degradation
Electrophoresis, Gel, Two-Dimensional
Amino Acid Sequence
Genes
Erythrocytes
Enzymes
Chemical analysis

Keywords

  • Macropain
  • Proteasome
  • Proteinase

ASJC Scopus subject areas

  • Structural Biology
  • Biophysics
  • Biochemistry
  • Molecular Biology

Cite this

Relationships among the subunits of the high molecular weight proteinase, macropain (proteasome). / Lee, Lawrence W.; Moomaw, Carolyn R.; Orth, Kim; McGuire, Michael J.; DeMartino, George N.; Slaughter, Clive A.

In: Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular, Vol. 1037, No. 2, 09.02.1990, p. 178-185.

Research output: Contribution to journalArticle

Lee, Lawrence W. ; Moomaw, Carolyn R. ; Orth, Kim ; McGuire, Michael J. ; DeMartino, George N. ; Slaughter, Clive A. / Relationships among the subunits of the high molecular weight proteinase, macropain (proteasome). In: Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular. 1990 ; Vol. 1037, No. 2. pp. 178-185.
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