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

机译:用血红素结合的荧光抑制剂可视化活细胞中的诱导型一氧化氮合酶

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摘要

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.
机译:一氧化氮合酶(NOS)生理学的研究受到缺乏合适的探针来检测活细胞或动物中NOS的限制。在这里,我们表征了一种称为PIF(嘧啶咪唑FITC)的荧光诱导型NOS(iNOS)抑制剂,并检查了其在活细胞中iNOS显微成像中的实用性。 PIF与iNOS的结合表现出高亲和力,同工型选择性和血红素特异性,并且本质上是不可逆的。 PIF用于成功成像在RAW264.7细胞,HEK293T细胞,人A549上皮细胞和新鲜获得的人肺上皮中表达的iNOS。 PIF用于估计iNOS在HEK293T细胞中的半衰期为1.8小时。我们的工作表明,像PIF这样的荧光探针对于研究iNOS细胞生物学以及了解涉及iNOS表达功能异常的疾病的病理生理学将非常有价值。

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