Molecular machines for protein degradation

被引:156
作者
Groll, M
Bochtler, M
Brandstetter, H
Clausen, T
Huber, R
机构
[1] LMU Munchen, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
[2] Max Planck Inst Biochem, Abt Strukturforsch, D-82152 Martinsried, Germany
关键词
molecular machines; proteasomes; protein degradation; protein structures; structure-activity relationships;
D O I
10.1002/cbic.200400313
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
One of the most precisely regulated processes in living cells is intracellular protein degradation. The main component of the degradation machinery is the 20S proteasome present in both eukaryotes and prokaryotes. In addition, there exist other proteasome-related protein-degradation machineries, like HsIVU in eubacteria. Peptides generated by proteosomes and related systems can be used by the cell, for example, for antigen presentation. However, most of the peptides must be degraded to single amino acids, which ore further used in cell metabolism and for the synthesis of new proteins. Tricorn protease and its interacting factors are working downstream of the proteasome and process the peptides into amino acids. Here, we summarise the current state of knowledge about protein-degradation systems, focusing in particular on the proteosome, HsIVU, Tricorn protease and its interacting factors and DegP The structural information about these protein complexes opens new possibilities for identifying, characterising. and elucidating the mode of action of natural and synthetic inhibitors, which affects their function. Some of these compounds may find therapeutic applications in contemporary medicine.
引用
收藏
页码:222 / 256
页数:35
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