NAD+激酶
Boosting(机器学习)
化学
计算生物学
生物
计算机科学
生物化学
酶
人工智能
作者
Stephen J. Gardell,Meghan Hopf,Asima Khan,Mauro Dispagna,E. Hampton Sessions,Rebecca Falter,Nidhi Kapoor,Jeanne K. Brooks,Jeffrey A. Culver,Chris Petucci,Chen-Ting Ma,Steven E. Cohen,Jun Tanaka,Emmanuel S. Burgos,Jennifer S. Hirschi,Steven R. Smith,Eduard Sergienko,Anthony B. Pinkerton
标识
DOI:10.1038/s41467-019-11078-z
摘要
Abstract Pharmacological strategies that boost intracellular NAD + are highly coveted for their therapeutic potential. One approach is activation of nicotinamide phosphoribosyltransferase (NAMPT) to increase production of nicotinamide mononucleotide (NMN), the predominant NAD + precursor in mammalian cells. A high-throughput screen for NAMPT activators and hit-to-lead campaign yielded SBI-797812, a compound that is structurally similar to active-site directed NAMPT inhibitors and blocks binding of these inhibitors to NAMPT. SBI-797812 shifts the NAMPT reaction equilibrium towards NMN formation, increases NAMPT affinity for ATP, stabilizes phosphorylated NAMPT at His247, promotes consumption of the pyrophosphate by-product, and blunts feedback inhibition by NAD + . These effects of SBI-797812 turn NAMPT into a “super catalyst” that more efficiently generates NMN. Treatment of cultured cells with SBI-797812 increases intracellular NMN and NAD + . Dosing of mice with SBI-797812 elevates liver NAD + . Small molecule NAMPT activators such as SBI-797812 are a pioneering approach to raise intracellular NAD + and realize its associated salutary effects.
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