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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Similar Intracellular Peptide Profile of TAP1/beta 2 Microglobulin Double-Knockout Mice and C57BL/6 Wild-Type Mice as Revealed by Peptidomic Analysis

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Author(s):
Castro, Leandro M. [1, 2] ; Berti, Denise A. [2] ; Russo, Lilian C. [2] ; Coelho, Veronica [3, 4] ; Gozzo, Fabio C. [5] ; Oliveira, Vitor [1] ; Ferro, Emer S. [2]
Total Authors: 7
Affiliation:
[1] Univ Fed Sao Paulo, Dept Biochem, BR-04044020 Sao Paulo - Brazil
[2] Inst Biomed Sci, Dept Dev & Cell Biol, BR-05508000 Sao Paulo - Brazil
[3] Univ Sao Paulo, Immunol Lab, Heart Inst InCor, Sch Med, BR-05403001 Sao Paulo - Brazil
[4] Natl Inst Sci & Technol, INCT Inst Invest Immunol 3, BR-05403001 Sao Paulo - Brazil
[5] Univ Estadual Campinas, Inst Chem, BR-13083970 Campinas, SP - Brazil
Total Affiliations: 5
Document type: Journal article
Source: AAPS JOURNAL; v. 12, n. 4, p. 608-616, DEC 2010.
Web of Science Citations: 11
Abstract

Cells produce and use peptides in distinctive ways. In the present report, using isotope labeling plus semi-quantitative mass spectrometry, we evaluated the intracellular peptide profile of TAP1/beta 2m(-/-) (transporter associated with antigen-processing 1/beta 2 microglobulin) double-knockout mice and compared it with that of C57BL/6 wild-type animals. Overall, 92 distinctive peptides were identified, and most were shown to have a similar concentration in both mouse strains. However, some peptides showed a modest increase or decrease (similar to 2-fold), whereas a glycine-rich peptide derived from the C-terminal of neurogranin (KGPGPGGPGGAGGARGGAGGGPSGD) showed a substantial increase (6-fold) in TAP1/beta 2m(-/-) mice. Thus, TAP1 and beta 2microglobulin have a small influence on the peptide profile of neuronal tissue, suggesting that the presence of peptides derived from intracellular proteins in neuronal tissue is not associated with antigens of the class I major histocompatibility complex. Therefore, it is possible that these intracellular peptides play a physiological role. (AU)

FAPESP's process: 10/00828-0 - Functional studies about intracellular oligopeptides and oligopeptidases and their possible physiopatological correlations
Grantee:Lilian Cristina Russo Vieira
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 04/04933-2 - Molecular cell biology of oligopeptidases
Grantee:Emer Suavinho Ferro
Support Opportunities: Research Projects - Thematic Grants