Friesen W J, Darby M K
Department of Microbiology and Immunology, Kimmel Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
Nat Struct Biol. 1998 Jul;5(7):543-6. doi: 10.1038/794.
A zinc finger library with degenerate alpha-helices was displayed on the surface of bacteriophage and proteins that bind human immunodeficiency virus type-1 (HIV-1) Rev response element stem loop IIB (RRE-IIB) RNA or 5S rRNA were isolated. DNA encoding affinity selected zinc fingers was shuffled by recombination in vitro to isolate proteins with higher RNA binding affinity. Proteins constructed in this way bind RNA specifically both in vitro and in vivo. These results demonstrate that RNA substrate specificity of zinc fingers can be changed through mutation of alpha-helices to construct novel RNA binding proteins.
一个具有简并α-螺旋的锌指文库展示在噬菌体表面,并分离出了结合人类免疫缺陷病毒1型(HIV-1)Rev反应元件茎环IIB(RRE-IIB)RNA或5S rRNA的蛋白质。编码经亲和力筛选的锌指的DNA通过体外重组进行改组,以分离出具有更高RNA结合亲和力的蛋白质。以这种方式构建的蛋白质在体外和体内均能特异性结合RNA。这些结果表明,锌指的RNA底物特异性可以通过α-螺旋的突变来改变,从而构建新型RNA结合蛋白。