使用炔基修饰的 CMP-唾液酸供体评估人类唾液基转移酶特异性的快速灵敏微板测定 (MPSA)。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Kiamungongo Clairene Filipe, Sushmaa Dangudubiyyam, Cédric Lion, Mathieu Decloquement, Roxana Elin Teppa, Christophe Biot, Anne Harduin-Lepers
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引用次数: 0

摘要

人类硅烷基转移酶主要利用 CMP-Sias,尤其是将 Neu5Ac 从 CMP-Neu5Ac 转移到各种受体上。化学生物学的进步导致了新型 CMP-Sia 给体的合成,适合在基于细胞的检测中进行生物正交反应。然而,这些供体与所有人类酶的兼容性仍不确定。我们合成了一种非天然的 CMP-Sia 供体,它在 Neu5Ac 的 N-酰基上进行了炔基修饰,能被人类 ST6Gal I 和 ST3Gal I 有效利用。所有被检测的酶都能耐受 CMP-SiaNAl,从而可以确定动力学参数和周转次数。这项研究加强了人类硅烷基转移酶的生物化学特征,为开发硅烷基转移酶抑制剂开辟了新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rapid and Sensitive MicroPlate Assay (MPSA) Using an Alkyne-Modified CMP-Sialic Acid Donor to Evaluate Human Sialyltransferase Specificity.

Human sialyltransferases primarily utilize CMP-Sias, especially transferring Neu5Ac from CMP-Neu5Ac to various acceptors. Advances in chemical biology have led to the synthesis of novel CMP-Sia donors suitable for bioorthogonal reactions in cell-based assays. However, the compatibility of these donors with all human enzymes remains uncertain. We synthesized a non-natural CMP-Sia donor with an alkyne modification on the N-acyl group of Neu5Ac, which was effectively used by human ST6Gal I and ST3Gal I. A sensitive MicroPlate Sialyltransferase Assay (MPSA) was developed and expanded to a panel of 13 human STs acting on glycoproteins. All assayed enzymes tolerated CMP-SiaNAl, allowing for the determination of kinetic parameters and turnover numbers. This study enhances the biochemical characterization of human sialyltransferases and opens new avenues for developing sialyltransferase inhibitors.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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