dna标记配体诱导细胞表型活性记录。

IF 4.2 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Philipp N. Sander, Jared T. Gillen Miller and Luke L. Lairson
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引用次数: 0

摘要

dna编码文库(DEL)能够以低成本和高速度搜索大量的遗传或化学空间,因此有助于基因组和小分子的发现。目前的DEL化学文库筛选方法主要集中在体外基于靶标的亲和力或活性。在这里,我们描述了一种方法来记录基于表型的dna编码的小分子在其同源条形码在活细胞中的活性。我们将携带光释放小分子的氯烷衍生DNA条形码转染到细胞中。光释放后,生物活性化合物诱导含有自标记HaloTag蛋白的报告基因盒的表达,该基因盒通过编码条形码进行共价修饰。我们证明,在免疫沉淀富集后,我们可以从接受活性化合物的细胞中恢复活性信息。这种可推广的方法应该使未来的策略能够在复杂的细胞或生物水平系统中促进基于表型的dna编码化学文库筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Induced cell phenotype activity recording of DNA-tagged ligands†

Induced cell phenotype activity recording of DNA-tagged ligands†

Based on their ability to canvas vast genetic or chemical space at low cost and high speed, DNA-encoded libraries (DEL) have served to enable both genomic and small molecule discovery. Current DEL chemical library screening approaches focus primarily on in vitro target-based affinity or activity. Here we describe an approach to record the phenotype-based activity of DNA-encoded small molecules on their cognate barcode in living cells. We transfected chloroalkane-derivatized DNA barcodes carrying photoreleasable small molecules into cells. Following photorelease, bioactive compounds induced expression of a reporter gene cassette containing self-labeling HaloTag protein that becomes covalently modified by encoding barcodes. We demonstrate that we can recover activity information from cells that received active compound following immunoprecipitation-based enrichment. This generalizable approach should enable future strategies that facilitate phenotype-based screens of DNA-encoded chemical libraries in complex cellular or organism level systems.

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来源期刊
CiteScore
6.10
自引率
0.00%
发文量
128
审稿时长
10 weeks
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