Srisawat Chatchawan, Engelke David R
Department of Biological Chemistry, University of Michigan, 3200 MSRB III, 1150 West Medical Center Drive, Ann Arbor 48109-0606, USA.
Methods. 2002 Feb;26(2):156-61. doi: 10.1016/S1046-2023(02)00018-X.
Intrinsic affinity tags are useful tools for the study of macromolecular targets. Although polypeptide affinity tags are routinely used in purification and detection of protein complexes, there has been a relative lack of powerful RNA affinity tags that can be embedded within RNA sequences. Here, the preparation and use of two RNA affinity tags against Sephadex or streptavidin are described. The two tags have different strengths that make them appropriate for slightly different uses. One is a high-affinity ligand for streptavidin that can be specifically eluted by competition with biotin under otherwise native binding conditions. The other tag binds selectively to Sephadex beads, and can be eluted by competition with the soluble dextran that composes Sephadex. When properly placed within another RNA molecule, the tags can be used to effect dramatic purification of RNA or ribonucleoprotein complexes from complex mixtures of cellular RNA.
内在亲和标签是研究大分子靶标的有用工具。尽管多肽亲和标签常用于蛋白质复合物的纯化和检测,但相对缺乏可嵌入RNA序列中的强大RNA亲和标签。在此,描述了针对葡聚糖凝胶或链霉亲和素的两种RNA亲和标签的制备和使用。这两种标签具有不同的亲和力,使其适用于略有不同的用途。一种是链霉亲和素的高亲和力配体,在其他天然结合条件下,可通过与生物素竞争而特异性洗脱。另一种标签选择性地结合葡聚糖凝胶珠,并可通过与构成葡聚糖凝胶的可溶性葡聚糖竞争而洗脱。当标签正确地置于另一个RNA分子中时,可用于从细胞RNA的复杂混合物中显著纯化RNA或核糖核蛋白复合物。