Swisher J, Duarte C M, Su L J, Pyle A M
Integrated Program in Cellular, Molecular, and Biophysical Studies, Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY, USA.
EMBO J. 2001 Apr 17;20(8):2051-61. doi: 10.1093/emboj/20.8.2051.
Group II introns are well recognized for their remarkable catalytic capabilities, but little is known about their three-dimensional structures. In order to obtain a global view of an active enzyme, hydroxyl radical cleavage was used to define the solvent accessibility along the backbone of a ribozyme derived from group II intron ai5gamma. These studies show that a highly homogeneous ribozyme population folds into a catalytically compact structure with an extensively internalized catalytic core. In parallel, a model of the intron core was built based on known tertiary contacts. Although constructed independently of the footprinting data, the model implicates the same elements for involvement in the catalytic core of the intron.
II 组内含子因其卓越的催化能力而广为人知,但对其三维结构却知之甚少。为了全面了解一种活性酶,采用了羟基自由基切割法来确定源自 II 组内含子 ai5γ 的核酶主链上的溶剂可及性。这些研究表明,高度均一的核酶群体折叠成具有广泛内化催化核心的催化紧密结构。同时,基于已知的三级相互作用构建了内含子核心的模型。尽管该模型是独立于足迹数据构建的,但它暗示了参与内含子催化核心的相同元件。