Solid-phase DNA-encoded library synthesis: a master builder's instructions.

IF 13.1 1区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Anjali Dixit, Brian M Paegel
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引用次数: 0

Abstract

Solid-phase DNA-encoded library (DEL) synthesis is a next-generation drug discovery technology with powerful activity-based and cellular lead identification capabilities. Solid-phase DELs combine the one-bead-one-compound approach with DNA encoding to furnish beads that display multiple copies of photocleavable library members and DNA encoding tags. Sequential chemical synthesis and enzymatic DNA ligation reactions yield an encoded library in which individual library members are physically isolable, enabling various high-throughput screening modalities. This advancement from on-DNA synthesis, in which small molecules are directly attached to their DNA-encoding tags, decouples the library member from the steric bulk of the DNA tag, which prevents biased binding to a target. Here we provide step-by-step instructions for solid-phase DEL synthesis, incorporating all of our most recent quality control innovations to ensure robust library production. The protocol begins with on-bead synthesis of a linker containing a spectroscopic handle for chromatographic analysis, an ionization enhancer for mass spectrometry and an alkyne for installation of DNA encoding sites via copper-catalyzed azide-alkyne cycloaddition click chemistry. Coupling of a photocleavable linker before library synthesis enables compound liberation from the bead for activity-based screening. Powerful combinatorial split-and-pool parallel synthesis tactics transform modest collections of small-molecule building blocks into large DELs of all possible building block combinations. Post synthesis, decoding and mass analysis of single DEL beads as well as whole-library deep sequencing provides rigorous chemical and bioinformatic quality control and establishes suitability for screening. The solid-phase chemistry is highly accessible: expertise in chemical synthesis is not necessary and solid-phase synthesis apparatus is routinely available in molecular biology laboratories. This procedure requires ~1 month to complete.

固相dna编码文库合成:建造大师的指令。
固相dna编码文库(DEL)合成是新一代药物发现技术,具有强大的基于活性和细胞先导物识别能力。固相DELs将一粒-一种化合物方法与DNA编码相结合,以提供显示可光切割文库成员和DNA编码标签的多个拷贝的珠。顺序化学合成和酶促DNA连接反应产生一个编码文库,其中单个文库成员在物理上是可分离的,从而实现各种高通量筛选方式。这一进步来自于DNA合成,其中小分子直接附着在它们的DNA编码标签上,将文库成员与DNA标签的空间体分离,从而防止了与目标的偏结合。在这里,我们为固相DEL合成提供一步一步的说明,结合我们所有最新的质量控制创新,以确保强大的库生产。该方案首先在头上合成一个连接体,其中包含用于色谱分析的光谱手柄,用于质谱分析的电离增强剂和用于通过铜催化叠氮化物-炔环加成点击化学安装DNA编码位点的炔。在文库合成之前,光可切割连接物的耦合使化合物从头中解放出来,用于基于活性的筛选。强大的组合分裂池并行合成策略将小分子构建块的适度集合转化为所有可能构建块组合的大型DELs。单DEL珠的合成后、解码和质量分析以及全文库深度测序提供了严格的化学和生物信息学质量控制,并建立了筛选的适用性。固相化学是非常容易获得的:不需要化学合成方面的专业知识,分子生物学实验室通常可以使用固相合成仪器。这个过程大约需要1个月才能完成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nature Protocols
Nature Protocols 生物-生化研究方法
CiteScore
29.10
自引率
0.70%
发文量
128
审稿时长
4 months
期刊介绍: Nature Protocols focuses on publishing protocols used to address significant biological and biomedical science research questions, including methods grounded in physics and chemistry with practical applications to biological problems. The journal caters to a primary audience of research scientists and, as such, exclusively publishes protocols with research applications. Protocols primarily aimed at influencing patient management and treatment decisions are not featured. The specific techniques covered encompass a wide range, including but not limited to: Biochemistry, Cell biology, Cell culture, Chemical modification, Computational biology, Developmental biology, Epigenomics, Genetic analysis, Genetic modification, Genomics, Imaging, Immunology, Isolation, purification, and separation, Lipidomics, Metabolomics, Microbiology, Model organisms, Nanotechnology, Neuroscience, Nucleic-acid-based molecular biology, Pharmacology, Plant biology, Protein analysis, Proteomics, Spectroscopy, Structural biology, Synthetic chemistry, Tissue culture, Toxicology, and Virology.
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