A general strategy to solve the phase problem in RNA crystallography

被引:85
作者
Keel, Amanda Y.
Rambo, Robert P.
Batey, Robert T.
Kieft, Jeffrey S. [1 ]
机构
[1] Univ Colorado Denver, Hlth Sci Ctr, Dept Biochem & Mol Genet, Aurora, CO 80045 USA
[2] Univ Colorado, Div Life Sci, Berkeley, CA 94720 USA
[3] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
关键词
D O I
10.1016/j.str.2007.06.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
X-ray crystallography of biologically important RNA molecules has been hampered by technical challenges, including finding heavy-atom derivatives to obtain high-quality experimental phase information. Existing techniques have drawbacks, limiting the rate at which important new structures are solved. To address this, we have developed a reliable means to localize heavy atoms specifically to virtually any RNA. By solving the crystal structures of thirteen variants of the G center dot U wobble pair cation binding motif, we have identified a version that when inserted into an RNA helix introduces a high-occupancy cation binding site suitable for phasing. This "directed soaking" strategy can be integrated fully into existing RNA crystallography methods, potentially increasing the rate at which important structures are solved and facilitating routine solving of structures using Cu-K alpha radiation. This method already has been used to solve several crystal structures.
引用
收藏
页码:761 / 772
页数:12
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