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模拟诱变体的结合:APOBEC 对核酸配体的选择。

Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands.

机构信息

OyaGen, Inc., 77 Ridgeland Road, Rochester, NY 14623, USA.

OyaGen, Inc., 77 Ridgeland Road, Rochester, NY 14623, USA; University of Rochester, School of Medicine and Dentistry, Department of Biochemistry and Biophysics, 601 Elmwood Avenue, Rochester, NY 14642, USA.

出版信息

Trends Biochem Sci. 2018 Aug;43(8):606-622. doi: 10.1016/j.tibs.2018.04.013. Epub 2018 May 23.

Abstract

The 11-member APOBEC (apolipoprotein B mRNA editing catalytic polypeptide-like) family of zinc-dependent cytidine deaminases bind to RNA and single-stranded DNA (ssDNA) and, in specific contexts, modify select (deoxy)cytidines to (deoxy)uridines. In this review, we describe advances made through high-resolution co-crystal structures of APOBECs bound to mono- or oligonucleotides that reveal potential substrate-specific binding sites at the active site and non-sequence-specific nucleic acid binding sites distal to the active site. We also discuss the effect of APOBEC oligomerization on functionality. Future structural studies will need to address how ssDNA binding away from the active site may enhance catalysis and the mechanism by which RNA binding may modulate catalytic activity on ssDNA.

摘要

APOBEC(载脂蛋白 B mRNA 编辑酶催化多肽样)家族由 11 个锌依赖性胞嘧啶脱氨酶组成,能与 RNA 和单链 DNA(ssDNA)结合,并在特定情况下将特定的(脱氧)胞嘧啶修饰为(脱氧)尿嘧啶。在这篇综述中,我们描述了通过与单核苷酸或寡核苷酸结合的 APOBEC 的高分辨率共晶结构所取得的进展,这些结构揭示了活性部位的潜在底物特异性结合位点,以及远离活性部位的非序列特异性核酸结合位点。我们还讨论了 APOBEC 寡聚化对功能的影响。未来的结构研究需要解决 ssDNA 结合远离活性部位如何增强催化作用,以及 RNA 结合如何调节 ssDNA 上的催化活性的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37d2/6073885/e8fde5aab262/gr1.jpg

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