Redox Control of 20S Proteasome Gating


Autoria(s): Silva, Gustavo M.; Netto, Luis E. S.; Simoes, Vanessa; Santos, Luiz F. A.; Gozzo, Fabio C.; Demasi, Marcos A. A.; Oliveira, Cristiano Luis Pinto de; Bicev, Renata Naporano; Klitzke, Clecio F.; Sogayar, Mari C.; Demasi, Marilene
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

14/10/2013

14/10/2013

2012

Resumo

The proteasome is the primary contributor in intracellular proteolysis. Oxidized or unstructured proteins can be degraded via a ubiquitin-and ATP-independent process by the free 20S proteasome (20SPT). The mechanism by which these proteins enter the catalytic chamber is not understood thus far, although the 20SPT gating conformation is considered to be an important barrier to allowing proteins free entrance. We have previously shown that S-glutathiolation of the 20SPT is a post-translational modification affecting the proteasomal activities. Aims: The goal of this work was to investigate the mechanism that regulates 20SPT activity, which includes the identification of the Cys residues prone to S-glutathiolation. Results: Modulation of 20SPT activity by proteasome gating is at least partially due to the S-glutathiolation of specific Cys residues. The gate was open when the 20SPT was S-glutathiolated, whereas following treatment with high concentrations of dithiothreitol, the gate was closed. S-glutathiolated 20SPT was more effective at degrading both oxidized and partially unfolded proteins than its reduced form. Only 2 out of 28 Cys were observed to be S-glutathiolated in the proteasomal alpha 5 subunit of yeast cells grown to the stationary phase in glucose-containing medium. Innovation: We demonstrate a redox post-translational regulatory mechanism controlling 20SPT activity. Conclusion: S-glutathiolation is a post-translational modification that triggers gate opening and thereby activates the proteolytic activities of free 20SPT. This process appears to be an important regulatory mechanism to intensify the removal of oxidized or unstructured proteins in stressful situations by a process independent of ubiquitination and ATP consumption. Antioxid. Redox Signal. 16, 1183-1194.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [08/06731-9, 07/58147-6]

Instituto Nacional de Ciencia, Tecnologia e Inovacao de Processos Redox em Biomedicina

Instituto Nacional de Ciencia, Tecnologia e Inovacao de Processos Redox em Biomedicina

Identificador

ANTIOXIDANTS & REDOX SIGNALING, NEW ROCHELLE, v. 16, n. 11, supl. 1, Part 1, pp. 1183-1194, JUN, 2012

1523-0864

http://www.producao.usp.br/handle/BDPI/35030

10.1089/ars.2011.4210

http://dx.doi.org/10.1089/ars.2011.4210

Idioma(s)

eng

Publicador

MARY ANN LIEBERT INC

NEW ROCHELLE

Relação

ANTIOXIDANTS & REDOX SIGNALING

Direitos

closedAccess

Copyright MARY ANN LIEBERT INC

Palavras-Chave #PROTEIN S-GLUTATHIONYLATION #26S PROTEASOME #OXIDATIVE STRESS #ALPHA-SYNUCLEIN #SELECTIVE DEGRADATION #ALZHEIMERS-DISEASE #OXIDIZED PROTEINS #SUBSTRATE ENTRY #CORE PARTICLE #UBIQUITIN #BIOCHEMISTRY & MOLECULAR BIOLOGY #ENDOCRINOLOGY & METABOLISM
Tipo

article

original article

publishedVersion