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一种高灵敏度和特异性的发光金属有机框架可测定一氧化氮的产生,并量化硫化氢对活细胞中一氧化氮的介导抑制作用。

A highly sensitive and specific luminescent MOF determines nitric oxide production and quantifies hydrogen sulfide-mediated inhibition of nitric oxide in living cells.

作者信息

Kumar Ajay, Negi Sheetal, Choudhury Tejaswini, Mutreja Vishal, Sunaina Sunaina, Sahoo Subash C, Singh Arjun, Mehta Surinder K, Kataria Ramesh, Saini Vikram

机构信息

Department of Chemistry and Centre for Advanced Studies in Chemistry, Punjab University, Chandigarh, 160014, India.

Laboratory of Infection Biology and Translational Research, Department of Biotechnology, All India Institute of Medical Sciences (AIIMS), New Delhi, 110029, India.

出版信息

Mikrochim Acta. 2023 Mar 10;190(4):127. doi: 10.1007/s00604-023-05660-y.

DOI:10.1007/s00604-023-05660-y
PMID:36897440
Abstract

The synthesis of a novel carboxylate-type organic linker-based luminescent MOF (Zn(HL) (L)) (named PUC2) (HL = 2-aminoterephtalic acid, L = 1-(3-aminopropyl) imidazole) is reported by the solvothermal method and comprehensively characterized using single-crystal XRD, PXRD, FTIR, TGA, XPS, FESEM, HRTEM, and BET. PUC2 selectively reacts with nitric oxide (NO) with a detection limit of 0.08 µM, and a quenching constant (0.5 × 10 M) indicating a strong interaction with NO. PUC2 sensitivity remains unaffected by cellular proteins or biologically relevant metals (Cu/ Fe/Mg/ Na/K/Zn), RNS/ROS, or HS to score NO in living cells. Lastly, we used PUC2 to demonstrate that HS inhibition increases NO production by ~ 14-30% in various living cells while exogenous HS suppresses NO production, indicating that the modulation of cellular NO production by HS is rather generic and not restricted to a particular cell type. In conclusion, PUC2 can successfully detect NO production in living cells and environmental samples with considerable potential for its application in improving the understanding of the role of NO in biological samples and study the inter-relationship between NO and HS.

摘要

通过溶剂热法报道了一种基于新型羧酸盐型有机连接体的发光金属有机框架材料(Zn(HL)(L))(命名为PUC2)(HL = 2-氨基对苯二甲酸,L = 1-(3-氨基丙基)咪唑),并使用单晶XRD、PXRD、FTIR、TGA、XPS、FESEM、HRTEM和BET对其进行了全面表征。PUC2与一氧化氮(NO)发生选择性反应,检测限为0.08 μM,猝灭常数为(0.5×10 M),表明与NO有强烈相互作用。PUC2的灵敏度不受细胞蛋白质或生物相关金属(铜/铁/镁/钠/钾/锌)、活性氮/活性氧或硫化氢的影响,可用于对活细胞中的NO进行评分。最后,我们使用PUC2证明,在各种活细胞中,硫化氢抑制可使NO生成增加约14 - 30%,而外源性硫化氢则抑制NO生成,这表明硫化氢对细胞内NO生成的调节具有普遍性,并不局限于特定细胞类型。总之,PUC2能够成功检测活细胞和环境样品中的NO生成,在增进对NO在生物样品中作用的理解以及研究NO与硫化氢的相互关系方面具有相当大的应用潜力。

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