Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, USA.
AbbVie, Inc., North Chicago, IL, USA.
Nat Chem. 2019 Jan;11(1):78-85. doi: 10.1038/s41557-018-0154-0. Epub 2018 Nov 5.
Conjugates between proteins and small molecules enable access to a vast chemical space that is not achievable with either type of molecule alone; however, the paucity of specific reactions capable of functionalizing proteins and natural products presents a formidable challenge for preparing conjugates. Here we report a strategy for conjugating electron-rich (hetero)arenes to polypeptides and proteins. Our bioconjugation technique exploits the electrophilic reactivity of an oxidized selenocysteine residue in polypeptides and proteins, and the electron-rich character of certain small molecules to provide bioconjugates in excellent yields under mild conditions. This conjugation chemistry enabled the synthesis of peptide-vancomycin conjugates without the prefunctionalization of vancomycin. These conjugates have an enhanced in vitro potency for resistant Gram-positive and Gram-negative pathogens. Additionally, we show that a 6 kDa affibody protein and a 150 kDa immunoglobulin-G antibody could be modified without diminishing bioactivity.
蛋白质和小分子之间的缀合物使我们能够进入一个仅使用任何一种类型的分子都无法达到的广阔化学空间;然而,能够对蛋白质和天然产物进行功能化的特定反应的缺乏,为制备缀合物带来了巨大的挑战。在这里,我们报告了一种将富电子(杂)芳族化合物与多肽和蛋白质连接的策略。我们的生物缀合技术利用了多肽和蛋白质中氧化硒半胱氨酸残基的亲电性反应性,以及某些小分子的富电子特性,在温和条件下以优异的收率提供生物缀合物。这种缀合化学使得在不预先对万古霉素进行官能化的情况下,也能够合成肽-万古霉素缀合物。这些缀合物对耐药的革兰氏阳性和革兰氏阴性病原体具有增强的体外活性。此外,我们还表明,即使在不降低生物活性的情况下,也可以修饰 6 kDa 的亲和体蛋白和 150 kDa 的免疫球蛋白 G 抗体。