Determination of the degree of PEGylation of protein bioconjugates using data from proton nuclear magnetic resonance spectroscopy

被引:7
|
作者
Zaghmi, Ahlem [1 ]
Greschner, Andrea A. [1 ]
Mendez-Villuendas, Eduardo [2 ]
Liu, Jun Yang [1 ]
de Haan, Hendrick W. [2 ]
Gauthier, Marc A. [1 ]
机构
[1] INRS, EMT Res Ctr, Varennes, PQ J3X 1S2, Canada
[2] Univ Ontario, Inst Technol, Fac Sci, Oshawa, ON L1H 7K4, Canada
来源
DATA IN BRIEF | 2019年 / 25卷
关键词
D O I
10.1016/j.dib.2019.104037
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The average number of methoxy poly(ethylene glycol) (mPEG) chains grafted to a protein - also known as the degree of PEGylation - is a fundamental parameter for characterizing a bioconjugate. The degree of PEGylation is typically determined by chromatographic or electrophoretic methods, which are subject to certain biases. This contribution describes an analytical approach alongside technical precautions for quantitatively determining the degree of PEGylation of protein bioconjugates by H-1 NMR spectroscopy. An accompanying dataset, corresponding to the raw H-1 NMR spectra of thirteen bioconjugates with different degrees of PEGylation and different mPEG molecular weights, is provided for the reader to become familiar with the analysis. The exemplary bioconjugate systemused in this Data article is the enzyme glutamate dehydrogenase (GDH) modified with multiple copies of mPEG (0.5-20 kDa). These bioconjugates correspond to those discussed in-depth in the article "Mechanismsof activity loss for amulti-PEGylated protein by experiment and simulation" by Zaghmi et al., 2019 The described approach to calculate degree of PEGylation is quantitative, applicable to other proteins, and can be adapted to other types of polymers. (C) 2019 The Authors. Published by Elsevier Inc.
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页数:7
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