Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
The Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Science. 2023 Mar 3;379(6635):939-945. doi: 10.1126/science.adf1354. Epub 2023 Mar 2.
Encoding small-molecule information in DNA has been leveraged to accelerate the discovery of ligands for therapeutic targets such as proteins. However, oligonucleotide-based encoding is hampered by inherent limitations of information stability and density. In this study, we establish abiotic peptides for next-generation information storage and apply them for the encoding of diverse small-molecule synthesis. The chemical stability of the peptide-based tag allows the use of palladium-mediated reactions to efficiently synthesize peptide-encoded libraries (PELs) with broad chemical diversity and high purity. We demonstrate the successful de novo discovery of small-molecule protein ligands from PELs by affinity selection against carbonic anhydrase IX and the oncogenic protein targets BRD4(1) and MDM2. Collectively, this work establishes abiotic peptides as carriers of information for the encoding of small-molecule synthesis, leveraged herein for the discovery of protein ligands.
将小分子信息编码到 DNA 中已被用于加速针对蛋白质等治疗靶点的配体的发现。然而,基于寡核苷酸的编码受到信息稳定性和密度固有限制的阻碍。在这项研究中,我们为下一代信息存储建立了非生物肽,并将其应用于多种小分子合成的编码。基于肽的标记的化学稳定性允许使用钯介导的反应来有效地合成具有广泛化学多样性和高纯度的肽编码文库 (PEL)。我们通过针对碳酸酐酶 IX 以及致癌蛋白靶标 BRD4(1) 和 MDM2 的亲和选择,证明了从小分子 PEL 中从头发现蛋白质配体的成功。总的来说,这项工作将非生物肽确立为小分子合成编码的信息载体,在此基础上用于发现蛋白质配体。