Preparation of hybrid (19S-20S-PA28) proteasome complexes and analysis of peptides generated during protein degradation

被引:28
作者
Cascio, P
Goldberg, AL
机构
来源
UBIQUITIN AND PROTEIN DEGRADATION, PART A | 2005年 / 398卷
关键词
D O I
10.1016/S0076-6879(05)98028-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
PA28 (also named REG or 11S) is a ring-shaped (180-kDa) interferon-gamma-induced complex that associates with the 20S proteasome and dramatically stimulates the breakdown of short peptides. Immunoprecipitation studies indicate that in vivo PA28 also exists in larger complexes that also contain the 19S particle, which is required for the ATP-ubiquitin-dependent degradation of proteins. However, because of its lability (e.g., it does not withstand exposure to high ionic strength buffers), this larger complex cannot be purified by standard biochemical protocols. Therefore, we developed a method to reconstitute in vitro such hybrid proteasomes (i.e., PA28-20S-19S) from highly purified components. This chapter describes conditions that allow the association of PA28 with "singly capped" 26S (i.e., 19S-20S) particles. In addition assays are described to measure absolute rates of degradation of several nonubiquitinated proteins by 26S and 20S proteasomes and methods to analyze the pattern and size distribution of peptides generated during the degradation of these proteins.
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页码:336 / 352
页数:17
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共 56 条
[1]  
AHN JY, 1995, FEBS LETT, V366, P37, DOI 10.1016/0014-5793(95)00492-R
[2]   Processive degradation of proteins and other catalytic properties of the proteasome from Thermoplasma acidophilum [J].
Akopian, TN ;
Kisselev, AF ;
Goldberg, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (03) :1791-1798
[3]   The proteasome:: Paradigm of a self-compartmentalizing protease [J].
Baumeister, W ;
Walz, J ;
Zühl, F ;
Seemuller, E .
CELL, 1998, 92 (03) :367-380
[4]   ATP hydrolysis by the proteasome regulatory complex PAN serves multiple functions in protein degradation [J].
Benaroudj, N ;
Zwickl, P ;
Seemüller, E ;
Baumeister, W ;
Goldberg, AL .
MOLECULAR CELL, 2003, 11 (01) :69-78
[5]   PAN, the proteasome-activating nucleotidase from archaebacteria, is a protein-unfolding molecular chaperone [J].
Benaroudj, N ;
Goldberg, AL .
NATURE CELL BIOLOGY, 2000, 2 (11) :833-839
[6]   The unfolding of substrates and ubiquitin-independent protein degradation by proteasomes [J].
Benaroudj, N ;
Tarcsa, E ;
Cascio, P ;
Goldberg, AL .
BIOCHIMIE, 2001, 83 (3-4) :311-318
[7]   Interferon-γ can stimulate post-proteasomal trimming of the N terminus of an antigenic peptide by inducing leucine aminopeptidase [J].
Beninga, J ;
Rock, KL ;
Goldberg, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (30) :18734-18742
[8]   The base of the proteasome regulatory particle exhibits chaperone-like activity [J].
Braun, BC ;
Glickman, M ;
Kraft, R ;
Dahlmann, B ;
Kloetzel, PM ;
Finley, D ;
Schmidt, M .
NATURE CELL BIOLOGY, 1999, 1 (04) :221-226
[9]   Properties of the hybrid form of the 26S proteasome containing both 19S and PA28 complexes [J].
Cascio, P ;
Call, M ;
Petre, BM ;
Walz, T ;
Goldberg, AL .
EMBO JOURNAL, 2002, 21 (11) :2636-2645
[10]   26S proteasomes and immunoproteasomes produce mainly N-extended versions of an antigenic peptide [J].
Cascio, P ;
Hilton, C ;
Kisselev, AF ;
Rock, KL ;
Goldberg, AL .
EMBO JOURNAL, 2001, 20 (10) :2357-2366