Analysis of Intracellular Substrates and Products of Thimet Oligopeptidase in Human Embryonic Kidney 293 Cells


Autoria(s): BERTI, Denise A.; MORANO, Cain; RUSSO, Lilian C.; CASTRO, Leandro M.; CUNHA, Fernanda M.; ZHANG, Xin; SIRONI, Juan; KLITZKE, Clecio F.; FERRO, Emer S.; FRICKER, Lloyd D.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2009

Resumo

Thimet oligopeptidase (EC 3.4.24.15; EP24.15) is an intracellular enzyme that has been proposed to metabolize peptides within cells, thereby affecting antigen presentation and G protein-coupled receptor signal transduction. However, only a small number of intracellular substrates of EP24.15 have been reported previously. Here we have identified over 100 peptides in human embryonic kidney 293 (HEK293) cells that are derived from intracellular proteins; many but not all of these peptides are substrates or products of EP24.15. First, cellular peptides were extracted from HEK293 cells and incubated in vitro with purified EP24.15. Then the peptides were labeled with isotopic tags and analyzed by mass spectrometry to obtain quantitative data on the extent of cleavage. A related series of experiments tested the effect of overexpression of EP24.15 on the cellular levels of peptides in HEK293 cells. Finally, synthetic peptides that corresponded to 10 of the cellular peptides were incubated with purified EP24.15 in vitro, and the cleavage was monitored by high pressure liquid chromatography and mass spectrometry. Many of the EP24.15 substrates identified by these approaches are 9-11 amino acids in length, supporting the proposal that EP24.15 can function in the degradation of peptides that could be used for antigen presentation. However, EP24.15 also converts some peptides into products that are 8-10 amino acids, thus contributing to the formation of peptides for antigen presentation. In addition, the intracellular peptides described here are potential candidates to regulate protein interactions within cells.

National Institutes of Health (NIH)[DK-51271]

National Institutes of Health (NIH)[DA-04494]

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[04/04933-2]

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[04/14846-0]

Financiadora de Estudos e Projetos (FINEP)[A-03/134]

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

CNPq Conselho Nacional de Pesquisa

Instituto UNIEMP

Pro-reitoria de Posgraduacao, Universidade de Sao Paulo (USP)

Identificador

JOURNAL OF BIOLOGICAL CHEMISTRY, v.284, n.21, p.14105-14116, 2009

0021-9258

http://producao.usp.br/handle/BDPI/24178

10.1074/jbc.M807916200

http://dx.doi.org/10.1074/jbc.M807916200

Idioma(s)

eng

Publicador

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Relação

Journal of Biological Chemistry

Direitos

restrictedAccess

Copyright AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Palavras-Chave #MHC CLASS-I #ANGIOTENSIN-CONVERTING ENZYME #ENDOPEPTIDASE EC 3.4.24.15 #ANTIGEN PRESENTATION #RAT-BRAIN #SOLUBLE METALLOENDOPEPTIDASE #QUANTITATIVE PEPTIDOMICS #DEGRADATION-PRODUCTS #PROTEIN-DEGRADATION #NATURAL REGULATORS #Biochemistry & Molecular Biology
Tipo

article

original article

publishedVersion