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PMID: 10514518 Published · ppublish English

An inducible nitric-oxide synthase (NOS)-associated protein inhibits NOS dimerization and activity.

The Journal of biological chemistry ·Vol. 274 ·No. 42 ·1999-10-15

Ratovitski EA, Bao C, Quick RA, McMillan A, Kozlovsky C, Lowenstein CJ

Abstract

A variety of transcriptional and post-transcriptional mechanisms regulate the expression of the inducible nitric-oxide synthase (iNOS, or NOS2). Although neurons and endothelial cells express proteins that interact with and inhibit neuronal NOS and endothelial NOS, macrophage proteins that inhibit NOS2 have not been identified. We show that murine macrophages express a 110-kDa protein that interacts with NOS2, which we call NOS-associated protein-110 kDa (NAP110). NAP110 directly interacts with the amino terminus of NOS2, and inhibits NOS catalytic activity by preventing formation of NOS2 homodimers. Expression of NAP110 may be a mechanism by which macrophages expressing NOS2 protect themselves from cytotoxic levels of nitric oxide.

Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1999-10-15
Language
English
Country/Region
United States
NLM ID
2985121R
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