1993
DOI: 10.1159/000468682
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Subunit Stoichiometry of Human Proteasomes

Abstract: Subunits from human placental proteasomes were separated by two-dimensional polyacrylamide gel electrophoresis. The amino acid composition of proteins from individual spots were determined. Some of the spots had identical amino acid compositions, confirming that they contain isoforms of the same subunit. Proteasomes from HeLa cells, labelled with 3Hleucine, were precipitated with an antibody and similarly separated into subunits. The radioactivity in each subunit was measured. The subunit stoichiometry was the… Show more

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Cited by 14 publications
(9 citation statements)
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“…Levels of α7 were two-fold higher in naked mole-rat lysates when compared to mice whereas α4 and β4 were three and four-fold higher in lysates from the longer lived species (Figure 4 A, B). These diverse trends in changes of the total content of constitutive and catalytic proteasome subunits that should exist in relatively equal amounts [9], [44] can be explained by upstream upregulation of the genes responsible for those protein products or by a mixed population of proteasome assemblies. To test the latter hypothesis, the contents of two immunoproteasome catalytic subunits β5i and β2i were also measured.…”
Section: Resultsmentioning
confidence: 99%
“…Levels of α7 were two-fold higher in naked mole-rat lysates when compared to mice whereas α4 and β4 were three and four-fold higher in lysates from the longer lived species (Figure 4 A, B). These diverse trends in changes of the total content of constitutive and catalytic proteasome subunits that should exist in relatively equal amounts [9], [44] can be explained by upstream upregulation of the genes responsible for those protein products or by a mixed population of proteasome assemblies. To test the latter hypothesis, the contents of two immunoproteasome catalytic subunits β5i and β2i were also measured.…”
Section: Resultsmentioning
confidence: 99%
“…The method used was that described by Hendil [41], with a few modifications. Briefly, 5 × 10 6 monolayer tumour cells were grown in 125 cm 2 tissue culture flasks (A/S Nunc) for 24 h with 15 ml Eagles' minimal essential medium supplemented with 5% FCS, 0 .…”
Section: Labelling and Immunoprecipitation Of Proteasome Subunitsmentioning
confidence: 99%
“…[26][27][28] The subtype pattern of these proteasomes analysed by high-resolution anionexchange chromatography comprises three subtypes designated HLI, HLII and HLIII Figure 1(a). Figure 1.…”
mentioning
confidence: 99%