Proteasome inhibitors: valuable new tools for cell biologists

被引:1275
作者
Lee, DH [1 ]
Goldberg, AL [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
D O I
10.1016/S0962-8924(98)01346-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Proteasomes are major sites for protein degradation in eukaryotic cells. The recent identification of selective proteasome inhibitors has allowed a definition of the roles of the ubiquitin-proteasome pathway in various cellular processes, such as antigen presentation and the degradation of regulatory or membrane proteins. This review describes the actions of these inhibitors, how they can be used to investigate cellular responses, the functions of the proteasome demonstrated by such studies and their potential applications in the future.
引用
收藏
页码:397 / 403
页数:7
相关论文
共 49 条
  • [1] Novel inhibitors of the proteasome and their therapeutic use in inflammation
    Adams, J
    Stein, R
    [J]. ANNUAL REPORTS IN MEDICINAL CHEMISTRY, VOL 31, 1996, 31 : 279 - 288
  • [2] Potent and selective inhibitors of the proteasome: Dipeptidyl boronic acids
    Adams, J
    Behnke, M
    Chen, SW
    Cruickshank, AA
    Dick, LR
    Grenier, L
    Klunder, JM
    Ma, YT
    Plamondon, L
    Stein, RL
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (04) : 333 - 338
  • [3] Interferon-γ can stimulate post-proteasomal trimming of the N terminus of an antigenic peptide by inducing leucine aminopeptidase
    Beninga, J
    Rock, KL
    Goldberg, AL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (30) : 18734 - 18742
  • [4] Beninga J, 1998, UBIQUITIN BIOL CELL, P191
  • [5] Covalent modification of the active site threonine of proteasomal beta subunits and the Escherichia coli homolog HslV by a new class of inhibitors
    Bogyo, M
    McMaster, JS
    Gaczynska, M
    Tortorella, D
    Goldberg, AL
    Ploegh, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) : 6629 - 6634
  • [6] ER-associated and proteasome-mediated protein degradation: How two topologically restricted events came together
    Brodsky, JL
    McCracken, AA
    [J]. TRENDS IN CELL BIOLOGY, 1997, 7 (04) : 151 - 156
  • [7] Bush KT, 1997, J BIOL CHEM, V272, P9086
  • [8] THE UBIQUITIN-PROTEASOME PROTEOLYTIC PATHWAY
    CIECHANOVER, A
    [J]. CELL, 1994, 79 (01) : 13 - 21
  • [9] Enzymes catalyzing ubiquitination and proteolytic processing of the p105 precursor of nuclear factor κB1
    Coux, O
    Goldberg, AL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (15) : 8820 - 8828
  • [10] Structure and functions of the 20S and 26S proteasomes
    Coux, O
    Tanaka, K
    Goldberg, AL
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 : 801 - 847