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PMID: 7722465 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Proteolytic processing is required for viral superantigen activity.

The Journal of experimental medicine ·Vol. 181 ·No. 5 ·1995-05-01 ·Pages 1899-904

Park CG, Jung MY, Choi Y, Winslow GM

Abstract

The mouse mammary tumor virus-7 superantigen (vSAG7) is proteolytically processed in B cells at as many as three positions. Proteolytic processing appears to be important for superantigen activity because a processed form of vSAG7 was predominant among those forms that were found to bind to major histocompatibility complex class II molecules. To determine the functional significance of proteolytic processing, a mutation was introduced in vSAG7 at one of the sites where proteolytic cleavage is thought to take place in B cells. Elimination of the putative processing site at position 171 abrogated detectable vSAG7 surface expression in B cells, indicating that proteolytic processing is required for vSAG7 function. Coexpression in insect cells of vSAG7 and furin, a proprotein-processing enzyme, also demonstrated that furin could process vSAG7 at position 171.

MeSH Terms
Amino Acid Sequence Animals Antigen Presentation Antigens, Viral/metabolism Base Sequence Furin Gammaretrovirus/immunology Molecular Sequence Data Spodoptera Subtilisins/metabolism Superantigens/metabolism Tumor Cells, Cultured
Chemicals
Antigens, Viral Superantigens Subtilisins Furin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Park C G
Rockefeller University, New York 10021, USA.
Jung M Y
Choi Y
Winslow G M
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1995-05-01
Pages
1899-904
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2192000
Subset
IM
Grants
NIAID NIH HHS · AI-17134 · United States
NIAID NIH HHS · AI-18785 · United States
NIAID NIH HHS · AI-22295 · United States
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