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通过功能筛选分析 Argonaute 引导 DNA 序列偏好性

Profiling Argonaute Guide DNA Sequence Preferences by Functional Screening.

作者信息

Hunt Eric A, Tamanaha Esta, Bonanno Kevin, Cantor Eric J, Tanner Nathan A

机构信息

Applications and Product Development, New England Biolabs, Ipswich, MA, United States.

Research, New England Biolabs, Ipswich, MA, United States.

出版信息

Front Mol Biosci. 2021 Apr 29;8:670940. doi: 10.3389/fmolb.2021.670940. eCollection 2021.

Abstract

Prokaryotic Argonautes (pAgo) are an increasingly well-studied class of guided endonucleases, and the underlying mechanisms by which pAgo generate nucleic acid guides remains an important topic of investigation. Recent insights into these mechanisms for the Argonaute protein from has drawn attention to global sequence and structural feature preferences involved in oligonucleotide guide selection. In this work, we approach the study of guide sequence preferences in Argonaute from a functional perspective. Screening a library of 1,968 guides against randomized single- and double-stranded DNA substrates, endonuclease activity associated with each guide was quantified using high-throughput capillary electrophoresis, and localized sequence preferences were identified which can be used to improve guide design for molecular applications. The most notable preferences include: a strong cleavage enhancement from a first position dT independent of target sequence; a significant decrease in activity with dA at position 12; and an impact of GC dinucleotides at positions 10 and 11. While this method has been useful in characterizing unique preferences of Argonaute and criteria for creating efficient guides, it could be expanded further to rapidly characterize more recent mesophilic variants reported in the literature and drive their utility toward molecular tools in biology and genome editing applications.

摘要

原核生物的Argonaute蛋白(pAgo)是一类研究日益深入的引导性核酸内切酶,pAgo产生核酸引导序列的潜在机制仍是一个重要的研究课题。最近对来自[具体来源未给出]的Argonaute蛋白这些机制的深入了解,引起了人们对寡核苷酸引导序列选择中全局序列和结构特征偏好的关注。在这项工作中,我们从功能角度研究了[具体物种未给出] Argonaute中引导序列的偏好。针对随机的单链和双链DNA底物筛选了一个包含1968个引导序列的文库,使用高通量毛细管电泳对与每个引导序列相关的核酸内切酶活性进行了定量,并确定了局部序列偏好,这些偏好可用于改进分子应用中的引导序列设计。最显著的偏好包括:第一位为dT时,无论靶序列如何,切割增强作用都很强;第12位为dA时,活性显著降低;第10位和第11位的GC二核苷酸有影响。虽然这种方法有助于表征[具体物种未给出] Argonaute的独特偏好以及创建有效引导序列的标准,但它可以进一步扩展,以快速表征文献中报道的更多近期嗜温变体,并推动它们在生物学分子工具和基因组编辑应用中的效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5672/8118625/fdfee2824abd/fmolb-08-670940-g001.jpg

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