用解毒寡核苷酸或核酸酶对细胞进行可逆性色素染色、分选和清洁(清洁荧光激活细胞分选),产生完全响应的细胞。

IF 4 2区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nucleic acid therapeutics Pub Date : 2024-02-01 Epub Date: 2024-01-30 DOI:10.1089/nat.2023.0050
Martin D Requena, Amy Yan, Telmo Llanga, Bruce A Sullenger
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引用次数: 0

摘要

在开发可控治疗药物时,能够逆转适配体与其靶蛋白的结合受到了广泛关注。最近,将适配体用作可逆的细胞分类配体也引发了人们的兴趣。抗体目前用于分离表达特定细胞表面受体的细胞。由于无法在分选后从分离细胞中去除抗体,这大大限制了抗体在许多应用中的效用。此前,我们曾介绍过一种特定的适配体-抗原寡核苷酸对如何分离细胞并清除它们。在这里,我们证明了这种方法的通用性;在荧光激活细胞分拣(FACS)过程中,适配体可以同时识别一种以上的细胞类型。此外,我们还介绍了使用核酸酶在细胞分拣后反向结合适配体的新方法。这种替代策略代表了一种无需为每种适配体生成解毒寡核苷酸的清洁方法,将大大降低清洁 FACS 的成本并扩大其用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reversible Aptamer Staining, Sorting, and Cleaning of Cells (Clean FACS) with Antidote Oligonucleotide or Nuclease Yields Fully Responsive Cells.

The ability to reverse the binding of aptamers to their target proteins has received considerable attention for developing controllable therapeutic agents. Recently, use of aptamers as reversible cell-sorting ligands has also sparked interest. Antibodies are currently utilized for isolating cells expressing a particular cell surface receptor. The inability to remove antibodies from isolated cells following sorting greatly limits their utility for many applications. Previously, we described how a particular aptamer-antidote oligonucleotide pair can isolate cells and clean them. Here, we demonstrate that this approach is generalizable; aptamers can simultaneously recognize more than one cell type during fluorescent activated cell sorting (FACS). Moreover, we describe a novel approach to reverse aptamer binding following cell sorting using a nuclease. This alternative strategy represents a cleaning approach that does not require the generation of antidote oligonucleotides for each aptamer and will greatly reduce the cost and expand the utility of Clean FACS.

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来源期刊
Nucleic acid therapeutics
Nucleic acid therapeutics BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
7.60
自引率
7.50%
发文量
47
审稿时长
>12 weeks
期刊介绍: Nucleic Acid Therapeutics is the leading journal in its field focusing on cutting-edge basic research, therapeutic applications, and drug development using nucleic acids or related compounds to alter gene expression. The Journal examines many new approaches for using nucleic acids as therapeutic agents or in modifying nucleic acids for therapeutic purposes including: oligonucleotides, gene modification, aptamers, RNA nanoparticles, and ribozymes.
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