Comprehensive analysis of insulin products complex disulfide bonds structure by high resolution mass spectrum
10.16438/j.0513-4870.2023-0284
- VernacularTitle:利用高分辨质谱技术综合解析胰岛素类制品复杂二硫键结构
- Author:
Xin-yue HU
;
Xiao-li DING
;
Yue SUN
;
Hui ZHANG
;
Jing LI
;
Cheng-gang LINAG
- Publication Type:Research Article
- Keywords:
insulin;
isulfide bond localization;
partial reduction alkylation;
in source decay;
electron transfer dissociation
- From:
Acta Pharmaceutica Sinica
2024;59(1):188-197
- CountryChina
- Language:Chinese
-
Abstract:
The correct pairing of disulfide bonds maintains the correct folding mode and high-level structure formation of peptides and protein drugs, which is crucial for the quality control of products. In order to ensure that the disulfide bonds are correctly paired, disulfide bond analysis is an essential part of peptides and protein drug characterization. Mass spectrometry can be used to analyze disulfide bonds. However, insulin and its analogues have two pairs of disulfide bonds without restriction enzyme cutting site. Conventional collision-induced dissociation (CID) and high-energy induced cleavage (HCD) cannot accurately locate the complex disulfide bond. In our study, three methods were used to localize the complex disulfide, including enzyme digestion combined with key peptide fragment in source decay (ISD) fragmentation method, enzyme digestion combined with partial reduction alkylation method, intact protein source ISD and electron transfer dissociation (ETD) cleavage method, The applicability of insulin aspart, insulin lispro and insulin glargine were also investigated. This study provides a new way for the quality control of disulfide bonding mode of insulin and its analogues, and also provides a reference for the disulfide bond localization of peptides or proteins containing this complex disulfide bond.
