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Dissecting the assembly pathway of the 20S proteasome
F Zühl1, E Seemüller, R Golbik
1Max-Planck-Institute for Biochemistry, Martinsried, Germany.
FEBS Letters
|December 31, 1997
Abstract:
Proteasomes reach their mature active state via a complex cascade of folding, assembly and processing events. The Rhodococcus proteasome offers a means to dissect the assembly pathway and to characterize intermediates; its four subunits (alpha1, alpha2, beta1, beta2) assemble efficiently in vitro with any combination of alpha and beta. Assembly studies with wild-type and N-terminally truncated beta-subunits in conjunction with refolding studies allowed to define the role of the propeptide which is two-fold: It supports the initial folding of the beta-subunits and it promotes the maturation of the holoproteasomes.