Lukasak Bradley J, Thompson Robert E, Mitchener Michelle M, Feng Vanessa J, Bagert John D, Muir Tom W
Department of Chemistry, Princeton University, Frick Chemistry Laboratory, Princeton, New Jersey 08544, United States.
ACS Cent Sci. 2022 Feb 23;8(2):176-183. doi: 10.1021/acscentsci.1c01332. Epub 2022 Feb 1.
Nucleosomes frequently exist as asymmetric species in native chromatin contexts. Current methods for the traceless generation of these heterotypic chromatin substrates are inefficient and/or difficult to implement. Here, we report an application of the SpyCatcher/SpyTag system as a convenient route to assemble desymmetrized nucleoprotein complexes. This genetically encoded covalent tethering system serves as an internal chaperone, maintained through the assembly process, affording traceless asymmetric nucleosomes following proteolytic removal of the tethers. The strategy allows for generation of nucleosomes containing asymmetric modifications on single or multiple histones, thereby providing facile access to a range of substrates. Herein, we use such constructs to interrogate how nucleosome desymmetrization caused by the incorporation of cancer-associated histone mutations alters chromatin remodeling processes. We also establish that our system provides access to asymmetric dinucleosomes, which allowed us to query the geometric/symmetry constraints of the unmodified histone H3 tail in stimulating the activity of the histone lysine demethylase, KDM5B. By providing a streamlined approach to generate these sophisticated substrates, our method expands the chemical biology toolbox available for interrogating the consequences of asymmetry on chromatin structure and function.
核小体在天然染色质环境中常以不对称形式存在。目前用于无痕生成这些异型染色质底物的方法效率低下且/或难以实施。在此,我们报道了SpyCatcher/SpyTag系统的一种应用,作为组装去对称化核蛋白复合物的便捷途径。这种基因编码的共价连接系统充当内部伴侣,在组装过程中得以维持,在蛋白酶去除连接子后可提供无痕不对称核小体。该策略允许生成在单个或多个组蛋白上含有不对称修饰的核小体,从而便于获得一系列底物。在此,我们使用此类构建体来探究由掺入癌症相关组蛋白突变引起的核小体去对称化如何改变染色质重塑过程。我们还证实,我们的系统能够获得不对称双核小体,这使我们能够探究未修饰组蛋白H3尾巴在刺激组蛋白赖氨酸去甲基化酶KDM5B活性方面的几何/对称限制。通过提供一种简化的方法来生成这些复杂的底物,我们的方法扩展了可用于探究不对称对染色质结构和功能影响的化学生物学工具箱。