Department of Chemistry, Ben-Gurion University of the Negev, Beer Sheva, Israel.
Angew Chem Int Ed Engl. 2012 Jul 9;51(28):6840-62. doi: 10.1002/anie.201200020. Epub 2012 Jun 13.
Ubiquitination is one of the most utilized posttranslational modifications in eukaryotes and is involved in a wide range of cellular processes, but is mostly known as a signal for proteasomal degradation. Recently, it has become clear that the ubiquitin signal is far more complex and is dictated by the ubiquitin component and the substrate. The remarkable diversity of the ubiquitin signaling process has triggered an incredible amount of effort to investigate the role of ubiquitination on biological processes. However, despite more than three decades of studies, several important questions remain unanswered. A major hurdle is the inability to obtain homogeneous ubiquitin bioconjugates in sufficient amounts from cells or by application of the enzymatic machinery. Recent breakthroughs in chemical and semisynthetic strategies, however, offer solutions to these challenges. In this Review, we survey the fundamental biological aspects of the ubiquitin signal and present the emerging non-enzymatic approaches for overcoming these obstacles.
泛素化是真核生物中最常用的翻译后修饰之一,参与广泛的细胞过程,但主要作为蛋白酶体降解的信号。最近,泛素信号远不止于此,其复杂程度取决于泛素组件和底物。泛素信号过程的显著多样性引发了人们极大的兴趣去研究泛素化在生物过程中的作用。然而,尽管经过了三十多年的研究,仍有几个重要的问题没有答案。一个主要的障碍是无法从细胞中获得足够量的均一的泛素生物缀合物,或通过应用酶机制来获得。然而,化学和半合成策略的最新突破为这些挑战提供了解决方案。在这篇综述中,我们调查了泛素信号的基本生物学方面,并提出了克服这些障碍的新兴非酶方法。