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毛细管电泳法自动化测定生物制药的 N-糖基化序列。

Automated N-Glycosylation Sequencing Of Biopharmaceuticals By Capillary Electrophoresis.

机构信息

Horváth Csaba Memorial Institute for Bioanalytical Research, MMKK, University of Debrecen, Debrecen, Nagyerdei krt 98, 4032, Hungary.

MTA-PE Translational Glycomics Research Group, Research Institute of Biomolecular and Chemical Engineering, University of Pannonia, Veszprém, Egyetem u. 10, 8200, Hungary.

出版信息

Sci Rep. 2017 Sep 15;7(1):11663. doi: 10.1038/s41598-017-11493-6.

Abstract

Comprehensive analysis of the N-linked carbohydrates of glycoproteins is gaining high recent interest in both the biopharmaceutical and biomedical fields. In addition to high resolution glycosylation profiling, sugar residue and linkage specific enzymes are also routinely used for exoglycosidase digestion based carbohydrate sequencing. This latter one, albeit introduced decades ago, still mostly practiced by following tedious and time consuming manual processes. In this paper we introduce an automated carbohydrate sequencing approach using the appropriate exoglycosidase enzymes in conjunction with the utilization of some of the features of a capillary electrophoresis (CE) instrument to speed up the process. The enzymatic reactions were accomplished within the temperature controlled sample storage compartment of a capillary electrophoresis unit and the separation capillary was also utilized for accurate delivery of the exoglycosidase enzymes. CE analysis was conducted after each digestion step obtaining in this way the sequence information of N-glycans in 60 and 128 minutes using the semi- and the fully-automated methods, respectively.

摘要

糖蛋白的 N-连接糖链的综合分析在生物制药和生物医学领域受到越来越多的关注。除了高分辨率的糖基化分析外,糖残基和连接特异性酶也常用于外切糖苷酶消化的基于碳水化合物测序。尽管这种方法几十年前就已经提出,但仍主要通过繁琐且耗时的手动过程来实施。在本文中,我们介绍了一种自动化的碳水化合物测序方法,该方法使用适当的外切糖苷酶酶,并结合毛细管电泳(CE)仪器的一些功能来加速该过程。酶反应在毛细管电泳单元的温度控制样品储存室中完成,分离毛细管也用于准确输送外切糖苷酶酶。在每个消化步骤后进行 CE 分析,从而分别在 60 分钟和 128 分钟内使用半自动和全自动方法获得 N-聚糖的序列信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c267/5600976/0c65b44158cc/41598_2017_11493_Fig1_HTML.jpg

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