On-line capillary isoelectric focusing hyphenated to native electrospray ionization mass spectrometry for the characterization of interferon-γ and variants

被引:21
作者
Przybylski, Cedric [1 ,2 ]
Mokaddem, Meriem [3 ,4 ,5 ,6 ]
Prull-Janssen, Mehdi [1 ,2 ]
Saesen, Els [7 ,8 ,9 ]
Lortat-Jacob, Hugues [7 ,8 ,9 ]
Gonnet, Florence [1 ,2 ]
Varenne, Anne [3 ,4 ,5 ,6 ]
Daniel, Regis [1 ,2 ]
机构
[1] CNRS, Lab Anal & Modelisat Biol & Environnem, UMR 8587, F-91025 Evry, France
[2] Univ Evry Val DEssonne, Lab Anal & Modelisat Biol & Environnem, UMR 8587, F-91025 Evry, France
[3] Ecole Natl Super Chim, Chim ParisTech, Unite Technol Chim & Biol Sante, F-75231 Paris, France
[4] CNRS, Unite Technol Chim & Biol Sante, UMR 8258, Paris, France
[5] Univ Paris 05, Unite Technol Chim & Biol Sante, Paris, France
[6] INSERM, Unite Technol Chim & Biol Sante 1022, Paris, France
[7] Univ Grenoble Alpes, IBS, Grenoble, France
[8] CNRS, IBS, Grenoble, France
[9] CEA, DSV, IBS, Grenoble, France
关键词
HEPARAN-SULFATE; CRYSTAL-STRUCTURE; BINDING; ELECTROPHORESIS; PROTEINS; AFFINITY; COMPLEX; ORGANIZATION; RESOLUTION; FUCOIDAN;
D O I
10.1039/c4an01305k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The on-line hyphenation of Capillary IsoElectric Focusing (CIEF) with ElectroSpray Ionization Mass Spectrometry (ESI/MS) has been carried out in a non-denaturing detection mode at the CIEF-MS interface. This CIEF-MS coupling methodology relied on the use of 40% glycerol-water medium as anticonvective agent in the CE capillary and the addition of 10 mM ammonium acetate buffer, pH 5, as a volatile aqueous sheath liquid. These CIEF-MS coupling conditions allowed the characterization of the highly basic cytokine human interferon-gamma (IFN-gamma) and its detection as a non-covalent homodimer (33 814.3 g mol(-1)) corresponding to the active form of this immune-regulatory protein. An experimental pI value of 9.95 was determined for the human IFN-gamma homodimer in these conditions. The CIEF-MS analysis of several variants bearing punctual or deletion mutations within the two D1 and D2 basic clusters at the C-terminal end of IFN-gamma revealed the different contribution of these domains to the charge properties of this heparan sulfate-binding protein.
引用
收藏
页码:543 / 550
页数:8
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