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Visualizing inducible nitric-oxide synthase in living cells with a heme-binding fluorescent inhibitor.


ABSTRACT: The study of nitric-oxide synthase (NOS) physiology is constrained by the lack of suitable probes to detect NOS in living cells or animals. Here, we characterized a fluorescent inducible NOS (iNOS) inhibitor called PIF (pyrimidine imidazole FITC) and examined its utility for microscopic imaging of iNOS in living cells. PIF binding to iNOS displayed high affinity, isoform selectivity, and heme specificity, and was essentially irreversible. PIF was used to successfully image iNOS expressed in RAW264.7 cells, HEK293T cells, human A549 epithelial cells, and freshly obtained human lung epithelium. PIF was used to estimate a half-life for iNOS of 1.8 h in HEK293T cells. Our work reveals that fluorescent probes like PIF will be valuable for studying iNOS cell biology and in understanding the pathophysiology of diseases that involve dysfunctional iNOS expression.

SUBMITTER: Panda K 

PROVIDER: S-EPMC1177357 | biostudies-literature | 2005 Jul

REPOSITORIES: biostudies-literature

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Visualizing inducible nitric-oxide synthase in living cells with a heme-binding fluorescent inhibitor.

Panda Koustubh K   Chawla-Sarkar Mamta M   Santos Cecile C   Koeck Thomas T   Erzurum Serpil C SC   Parkinson John F JF   Stuehr Dennis J DJ  

Proceedings of the National Academy of Sciences of the United States of America 20050708 29


The study of nitric-oxide synthase (NOS) physiology is constrained by the lack of suitable probes to detect NOS in living cells or animals. Here, we characterized a fluorescent inducible NOS (iNOS) inhibitor called PIF (pyrimidine imidazole FITC) and examined its utility for microscopic imaging of iNOS in living cells. PIF binding to iNOS displayed high affinity, isoform selectivity, and heme specificity, and was essentially irreversible. PIF was used to successfully image iNOS expressed in RAW2  ...[more]

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