Small molecule inhibitors of mammalian glycosylation

Q1 Medicine Matrix Biology Plus Pub Date : 2022-12-01 DOI:10.1016/j.mbplus.2022.100108
Karim Almahayni , Malte Spiekermann , Antonio Fiore , Guoqiang Yu , Kayvon Pedram , Leonhard Möckl
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引用次数: 5

Abstract

Glycans are one of the fundamental biopolymers encountered in living systems. Compared to polynucleotide and polypeptide biosynthesis, polysaccharide biosynthesis is a uniquely combinatorial process to which interdependent enzymes with seemingly broad specificities contribute. The resulting intracellular cell surface, and secreted glycans play key roles in health and disease, from embryogenesis to cancer progression. The study and modulation of glycans in cell and organismal biology is aided by small molecule inhibitors of the enzymes involved in glycan biosynthesis. In this review, we survey the arsenal of currently available inhibitors, focusing on agents which have been independently validated in diverse systems. We highlight the utility of these inhibitors and drawbacks to their use, emphasizing the need for innovation for basic research as well as for therapeutic applications.

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哺乳动物糖基化的小分子抑制剂
聚糖是生命系统中遇到的基本生物聚合物之一。与多核苷酸和多肽生物合成相比,多糖生物合成是一个独特的组合过程,其中相互依赖的酶具有广泛的特异性。由此产生的细胞内细胞表面和分泌的聚糖在健康和疾病中发挥关键作用,从胚胎发生到癌症进展。聚糖在细胞和有机体生物学中的研究和调节是由参与聚糖生物合成的酶的小分子抑制剂辅助的。在这篇综述中,我们调查了目前可用的抑制剂库,重点是在不同系统中独立验证的药物。我们强调了这些抑制剂的效用及其使用的缺点,强调了基础研究和治疗应用的创新需求。
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来源期刊
Matrix Biology Plus
Matrix Biology Plus Medicine-Histology
CiteScore
9.00
自引率
0.00%
发文量
25
审稿时长
105 days
期刊最新文献
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