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Sökning: id:"swepub:oai:lup.lub.lu.se:f8243a88-6d96-45e3-90d2-d230299a8157" > Distinct difference...

Distinct differences in association of MHC class I with endoplasmic reticulum proteins in wild-type, and beta 2-microglobulin- and TAP-deficient cell lines

Paulsson, K M (författare)
Lund University,Lunds universitet,Antigen presentation,Forskargrupper vid Lunds universitet,Antigen Presentation,Lund University Research Groups
Wang, P (författare)
Lund University
Anderson, P O (författare)
Lund University,Lunds universitet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups
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Chen, Shangwu (författare)
Lund University
Pettersson, R F (författare)
Li, S (författare)
Lund University,Lunds universitet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups,Brunel University London
visa färre...
 (creator_code:org_t)
2001-08
2001
Engelska 11 s.
Ingår i: International Immunology. - : Oxford University Press (OUP). - 0953-8178 .- 1460-2377. ; 13:8, s. 73-1063
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • In this study we have compared the interaction of human MHC class I molecules with IgG heavy chain (HC) binding protein (BiP), calnexin, calreticulin, tapasin and TAP in beta(2)-microglobulin (beta(2)m)- or TAP-deficient cells, as well as in wild-type B-LCL cells. Distinct differences between the association of HC and these endoplasmic reticulum (ER) proteins were found in the three cell lines. In the absence of beta(2)m (Daudi cells), HC associated with both BiP and calnexin. A prominent portion of HC was complexed simultaneously to both chaperones, as indicated by co-precipitation with either anti-calnexin or anti-class I antisera. In the presence of beta(2)m, but absence of TAP (T2 cells), HC could be co-precipitated with calnexin, whereas no detectable interaction with BiP could be demonstrated. This suggests that calnexin interacts with HC at a later stage than BiP. In B-LCL cells, HC-beta(2)m associated with calreticulin and tapasin, whereas no interaction with calnexin and BiP was observed. In the absence of beta(2)m, HC were rapidly degraded in the ER, while the ER retained HC were stabilized in the presence of beta(2)m, even in the absence of TAP. The dissociation of class I molecules from TAP in B-LCL cells correlated with the kinetics of appearance of class I molecules on the cell surface, suggesting that TAP retains peptide-free class I molecules in the ER. Taken together, our results suggest the model that BiP and calnexin sequentially control the folding of MHC class I, before MHC class I molecules associate with the loading complex.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

ATP-Binding Cassette Transporters
Antiporters
Biological Transport
Calcium-Binding Proteins
Calnexin
Calreticulin
Carrier Proteins
Dimerization
Endoplasmic Reticulum
HLA Antigens
Heat-Shock Proteins
Histocompatibility Antigens Class I
Humans
Immunoglobulin G
Immunoglobulins
Membrane Transport Proteins
Molecular Chaperones
Ribonucleoproteins
Tumor Cells, Cultured
beta 2-Microglobulin
Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
tapasin

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Av författaren/redakt...
Paulsson, K M
Wang, P
Anderson, P O
Chen, Shangwu
Pettersson, R F
Li, S
Om ämnet
MEDICIN OCH HÄLSOVETENSKAP
MEDICIN OCH HÄLS ...
och Medicinska och f ...
och Cell och molekyl ...
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Lunds universitet

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