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Crystallization and preliminary diffraction analysis of a group I ribozyme from bacteriophage Twort

机译:噬菌体Twort中I族核酶的结晶和初步衍射分析

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摘要

Group I introns are catalytic RNAs that are capable of performing a variety of phosphotransesterification reactions including self-splicing and RNA cleavage. The reactions are efficient, accurate and dependent only on the presence of guanosine-nucleotide substrate and sufficient magnesium ion to stabilize the structure of the RNA. To understand how the group I intron active-site facilitates catalysis, crystals of a 242-nucleotide ribozyme bound to a four-nucleotide product RNA have been produced that diffract to 3.6 Å resolution. The space group of these crystals is I212121 and the unit-cell parameters are a = 94.6, b = 141.0, c = 210.9 Å. A single heavy-atom derivative has been synthesized by covalent modification of the product RNA with iodine.
机译:第I组内含子是催化RNA,能够进行多种磷酸酯交换反应,包括自剪切和RNA裂解。该反应是有效,准确的,并且仅取决于鸟苷核苷酸底物的存在和足够的镁离子来稳定RNA的结构。为了解第I组内含子的活性位点如何促进催化作用,已产生了一种结合到四核苷酸产物RNA上的242核苷酸核酶的晶体,其衍射分辨率达到3.6。这些晶体的空间群是I212121,晶胞参数是a = 94.6,b = 141.0,c = 210.9。通过将产物RNA与碘共价修饰,合成了单个重原子衍生物。

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