Purification, crystallization, and X-ray analysis of the yeast 20S proteasome.

Abstract:

:Intracellular protein degradation is one of the most precisely regulated processes in living cells. The main component of the degradation machinery is the 20S proteasome present in eukaryotes as well as in prokaryotes. We have developed successful purification protocols for the 20S proteasome in its native state using an affinity tag strategy. This chapter describes in detail the purification protocols, proteolytic activity assays, crystallization, and structure determination for the yeast 20S proteasome. The crystal structure of the eukaryotic proteasome opens new possibilities for identifying, characterizing, and elucidating the mode of action for natural and synthetic inhibitors, which affect its function. Some of these compounds may find therapeutic applications in contemporary medicine.

journal_name

Methods Enzymol

journal_title

Methods in enzymology

authors

Groll M,Huber R

doi

10.1016/S0076-6879(05)98027-0

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

329-36

eissn

0076-6879

issn

1557-7988

pii

S0076-6879(05)98027-0

journal_volume

398

pub_type

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