Holden Jeffrey K, Lewis Matthew C, Cinelli Maris A, Abdullatif Ziad, Pensa Anthony V, Silverman Richard B, Poulos Thomas L
Department of Molecular Biology and Biochemistry, ‡Department of Pharmaceutical Sciences, and §Department of Chemistry, University of California , Irvine, California 92697-3900, United States.
Departments of Chemistry and Molecular Biosciences, ⊥Chemistry of Life Processes Institute, and #Center for Molecular Innovation and Drug Discovery, Northwestern University , Evanston, Illinois 60208-3113, United States.
Biochemistry. 2016 Oct 4;55(39):5587-5594. doi: 10.1021/acs.biochem.6b00786. Epub 2016 Sep 21.
Nitric oxide is produced in Gram-positive pathogens Bacillus anthracis and Staphylococcus aureus by the bacterial isoform of nitric oxide synthase (NOS). Inhibition of bacterial nitric oxide synthase (bNOS) has been identified as a promising antibacterial strategy for targeting methicillin-resistant S. aureus [Holden, J. K., et al. (2015) Chem. Biol. 22, 785-779]. One class of NOS inhibitors that demonstrates antimicrobial efficacy utilizes an aminoquinoline scaffold. Here we report on a variety of aminoquinolines that target the bacterial NOS active site, in part, by binding to a hydrophobic patch that is unique to bNOS. Through mutagenesis and crystallographic studies, our findings demonstrate that aminoquinolines are an excellent scaffold for further aiding in the development of bNOS specific inhibitors.
一氧化氮由一氧化氮合酶(NOS)的细菌同工型在革兰氏阳性病原体炭疽芽孢杆菌和金黄色葡萄球菌中产生。抑制细菌一氧化氮合酶(bNOS)已被确定为一种有前景的抗甲氧西林耐药金黄色葡萄球菌的抗菌策略[霍尔登,J.K.等人(2015年)《化学生物学》22卷,785 - 779页]。一类具有抗菌功效的NOS抑制剂利用了氨基喹啉支架。在此我们报告了多种靶向细菌NOS活性位点的氨基喹啉,部分是通过与bNOS特有的疏水区域结合来实现的。通过诱变和晶体学研究,我们的发现表明氨基喹啉是进一步辅助开发bNOS特异性抑制剂的优良支架。