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- W2021036397 abstract "The physiological roles of insulin and nitric oxide (NO) have been recently recognized by several studies. A diversity of chemical modifications of insulin is reported both in vivo and in vitro. S-nitrosation, the covalent linkage of NO to cysteine free thiol is recognized as an important post-translational regulation in many proteins. Here we report the in vitro synthesis of an S-nitrosothiol of bovine insulin A- and B-chains. These compounds were characterized by their HPLC chromatographic behavior, monitored by UV visible spectroscopy and electron spray ionization mass spectrometry. The experimental results indicate that each A- and B-chain were S- nitrosated with only one NO group. Stability and solubility of these synthesized derivatives is described for physiological purposes. In this work, nitroso A- and B-chains of insulin were synthesized in vitro in order to better understand the possible interactions between insulin and NO that may be involved in the etiology of insulin resistance." @default.
- W2021036397 created "2016-06-24" @default.
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- W2021036397 date "2006-10-01" @default.
- W2021036397 modified "2023-09-27" @default.
- W2021036397 title "In Vitro Nitrosation of Insulin A- and B-Chains" @default.
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- W2021036397 doi "https://doi.org/10.1255/ejms.835" @default.
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