Laboratory of Genetically Encoded Small Molecules, The Rockefeller University, 1230 York Avenue, New York, New York 10065, United States.
Org Lett. 2024 May 31;26(21):4433-4437. doi: 10.1021/acs.orglett.4c00999. Epub 2024 May 20.
Most biosynthetic gene clusters (BGCs) are functionally inaccessible by using fermentation methods. Bioinformatic-coupled total synthesis provides an alternative approach for accessing BGC-encoded bioactivities. To date, synthetic bioinformatic natural product (synBNP) methods have focused on lipopeptides containing simple lipids. Here we increase the bioinformatic and synthetic complexity of the synBNP approach by targeting BGCs that encode -cinnamoyl lipids. This led to our synthesis of cinnamosyn, a 10-mer -cinnamoyl-containing peptide that is cytotoxic to human cells.
大多数生物合成基因簇(BGCs)通过发酵方法无法获得功能。生物信息学耦合的全合成提供了一种获得 BGC 编码生物活性的替代方法。迄今为止,合成生物信息学天然产物(synBNP)方法主要集中在含有简单脂质的脂肽上。在这里,我们通过针对编码 -肉桂酰脂质的 BGC 来增加 synBNP 方法的生物信息学和合成复杂性。这导致我们合成了 cinnamosyn,一种含有 10 个氨基酸的 -肉桂酰肽,对人类细胞具有细胞毒性。