New York University School of Medicine, Department of Microbiology, 550 First Avenue, MSB 236, New York, NY 10016.
Microbiol Spectr. 2014 Oct;2(5). doi: 10.1128/microbiolspec.MGM2-0008-2013.
Proteasomes are ATP-dependent, barrel-shaped proteases found in all three domains of life. In eukaryotes, proteins are typically targeted for degradation by posttranslational modification with the small protein ubiquitin. In 2008, the first bacterial protein modifier, Pup (prokaryotic ubiquitin-like protein), was identified in Mycobacterium tuberculosis. Functionally analogous to ubiquitin, conjugation with Pup serves as a signal for degradation by the mycobacterial proteasome. Proteolysis-dependent and -independent functions of the M. tuberculosis proteasome are essential for virulence of this successful pathogen. In this article we describe the discovery of the proteasome as a key player in tuberculosis pathogenesis and the biology and biochemistry of the Pup-proteasome system.
蛋白酶体是一种依赖于 ATP 的桶状蛋白酶,存在于所有三个生命领域中。在真核生物中,蛋白质通常通过与小蛋白泛素的翻译后修饰来靶向降解。2008 年,第一个细菌蛋白修饰物 Pup(原核泛素样蛋白)在结核分枝杆菌中被鉴定出来。与泛素功能类似,与 Pup 的缀合作为被分枝杆菌蛋白酶体降解的信号。结核分枝杆菌蛋白酶体的蛋白水解依赖性和非依赖性功能对这种成功病原体的毒力至关重要。在本文中,我们描述了蛋白酶体作为结核病发病机制中的关键因素的发现,以及 Pup-蛋白酶体系统的生物学和生物化学。