Peterson Craig L
Cold Spring Harb Protoc. 2009 Apr;2009(4):pdb.prot5115. doi: 10.1101/pdb.prot5115.
The goal of chromatin assembly procedures is to prepare extended nucleosomal arrays from cloned DNA templates and purified core and linker histones. The assembled chromatin should be highly defined in its protein content and resemble bulk chromatin isolated from living cell nuclei in terms of periodicity and nucleosome positioning. This protocol describes the preparation of Drosophila ACF (ATP-utilizing chromatin assembly and remodeling factor) for use in chromatin assembly reactions. In this method, ACF is prepared by the coexpression of the carboxyl-terminally FLAG-tagged Acf1 subunit with the untagged ISWI subunit in baculovirus. The complex is then purified in one step by FLAG immunoaffinity chromatography. This procedure typically results in a stoichiometric complex of Acf1 and ISWI.
染色质组装程序的目标是从克隆的DNA模板以及纯化的核心组蛋白和连接组蛋白制备延伸的核小体阵列。组装好的染色质在蛋白质含量上应高度明确,并且在周期性和核小体定位方面类似于从活细胞核中分离出的整体染色质。本方案描述了用于染色质组装反应的果蝇ACF(利用ATP的染色质组装和重塑因子)的制备方法。在此方法中,通过在杆状病毒中共同表达羧基末端带有FLAG标签的Acf1亚基和未标记的ISWI亚基来制备ACF。然后通过FLAG免疫亲和层析一步纯化该复合物。此程序通常会产生化学计量的Acf1和ISWI复合物。