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用基于氨基喹啉的抑制剂靶向细菌一氧化氮合酶

Targeting Bacterial Nitric Oxide Synthase with Aminoquinoline-Based Inhibitors.

作者信息

Holden Jeffrey K, Lewis Matthew C, Cinelli Maris A, Abdullatif Ziad, Pensa Anthony V, Silverman Richard B, Poulos Thomas L

机构信息

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.

出版信息

Biochemistry. 2016 Oct 4;55(39):5587-5594. doi: 10.1021/acs.biochem.6b00786. Epub 2016 Sep 21.

Abstract

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.

摘要

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。

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本文引用的文献

2
Nitric Oxide Synthase as a Target for Methicillin-Resistant Staphylococcus aureus.
Chem Biol. 2015 Jun 18;22(6):785-92. doi: 10.1016/j.chembiol.2015.05.013.
3
Inhibitor Bound Crystal Structures of Bacterial Nitric Oxide Synthase.
Biochemistry. 2015 Jul 7;54(26):4075-82. doi: 10.1021/acs.biochem.5b00431. Epub 2015 Jun 23.
4
Structure-based design of bacterial nitric oxide synthase inhibitors.
J Med Chem. 2015 Jan 22;58(2):994-1004. doi: 10.1021/jm501723p. Epub 2015 Jan 6.
5
Identification of redox partners and development of a novel chimeric bacterial nitric oxide synthase for structure activity analyses.
J Biol Chem. 2014 Oct 17;289(42):29437-45. doi: 10.1074/jbc.M114.595165. Epub 2014 Sep 6.
6
Simplified 2-aminoquinoline-based scaffold for potent and selective neuronal nitric oxide synthase inhibition.
J Med Chem. 2014 Feb 27;57(4):1513-30. doi: 10.1021/jm401838x. Epub 2014 Feb 10.
7
Structural and biological studies on bacterial nitric oxide synthase inhibitors.
Proc Natl Acad Sci U S A. 2013 Nov 5;110(45):18127-31. doi: 10.1073/pnas.1314080110. Epub 2013 Oct 21.
9
iMOSFLM: a new graphical interface for diffraction-image processing with MOSFLM.
Acta Crystallogr D Biol Crystallogr. 2011 Apr;67(Pt 4):271-81. doi: 10.1107/S0907444910048675. Epub 2011 Mar 18.
10
Features and development of Coot.
Acta Crystallogr D Biol Crystallogr. 2010 Apr;66(Pt 4):486-501. doi: 10.1107/S0907444910007493. Epub 2010 Mar 24.

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