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抗病毒核苷、环二核苷酸和寡核苷酸疗法的生物催化合成

Biocatalytic Synthesis of Antiviral Nucleosides, Cyclic Dinucleotides, and Oligonucleotide Therapies.

作者信息

Van Giesen Kyle J D, Thompson Matthew J, Meng Qinglong, Lovelock Sarah L

机构信息

Manchester Institute of Biotechnology, School of Chemistry, University of Manchester, 131 Princess Street, Manchester M1 7DN, U.K.

出版信息

JACS Au. 2022 Nov 30;3(1):13-24. doi: 10.1021/jacsau.2c00481. eCollection 2023 Jan 23.

Abstract

Nucleosides, nucleotides, and oligonucleotides modulate diverse cellular processes ranging from protein production to cell signaling. It is therefore unsurprising that synthetic analogues of nucleosides and their derivatives have emerged as a versatile class of drug molecules for the treatment of a wide range of disease areas. Despite their great therapeutic potential, the dense arrangements of functional groups and stereogenic centers present in nucleic acid analogues pose a considerable synthetic challenge, especially in the context of large-scale manufacturing. Commonly employed synthetic methods rely on extensive protecting group manipulations, which compromise step-economy and result in high process mass intensities. Biocatalytic approaches have the potential to address these limitations, enabling the development of more streamlined, selective, and sustainable synthetic routes. Here we review recent achievements in the biocatalytic manufacturing of nucleosides and cyclic dinucleotides along with progress in developing enzymatic strategies to produce oligonucleotide therapies. We also highlight opportunities for innovations that are needed to facilitate widespread adoption of these biocatalytic methods across the pharmaceutical industry.

摘要

核苷、核苷酸和寡核苷酸可调节从蛋白质生产到细胞信号传导等多种细胞过程。因此,核苷及其衍生物的合成类似物已成为一类用于治疗广泛疾病领域的通用药物分子,这并不奇怪。尽管它们具有巨大的治疗潜力,但核酸类似物中存在的官能团和立体中心的密集排列带来了相当大的合成挑战,尤其是在大规模生产的背景下。常用的合成方法依赖于广泛的保护基操作,这会影响步骤经济性并导致高过程质量强度。生物催化方法有潜力解决这些限制,从而开发出更简化、更具选择性和更可持续的合成路线。在此,我们综述了核苷和环状二核苷酸生物催化制造方面的最新成果,以及开发用于生产寡核苷酸疗法的酶策略的进展。我们还强调了促进这些生物催化方法在制药行业广泛应用所需的创新机会。

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