4.7 Article

Reconstitution of hybrid proteasomes from purified PA700-20 S complexes and PA28αβ activator:: Ultrastructure and peptidase activities

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JOURNAL OF MOLECULAR BIOLOGY
卷 313, 期 3, 页码 465-471

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ACADEMIC PRESS LTD
DOI: 10.1006/jmbi.2001.5063

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human; proteasome; activator; hybrid; electron microscopy

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The activity of the proteasome, the major non-lysosomal proteinase in eukaryotes, is stimulated by two activator complexes, PA700 and PA28. PA700-20 S-PA700 proteasorne complexes, generally designated as 26 S proteasomes, degrade proteins, whereas complexes of the type PA28-20 S-PA28 degrade only peptides. We report, for the first time; the in vitro reconstitution of previously identified hybrid proteasomes (PA700-20 S-PA28) from purified PA700-20 S proteasome complexes and PA28 activator. In electron micrographs, the hybrid appears as a corkscrew-shaped particle with a PA700 and a PA28 activator each bound to a terminal a-disk of the 20 S core proteasome. The multiple peptidase activities of hybrid proteasomes are not different from those of PA28-20 S-PA28 or PA700-20 S-PA700 complexes.

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