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Methods development for analysis of partially deglycosylated proteins and application to an HIV envelope protein vaccine candidate
被引:9
作者:
Go, Eden P.
[1
]
Hewawasam, Geetha S.
[1
]
Ma, Ben J.
[2
]
Liao, Hua-Xin
[2
]
Haynes, Barton F.
[2
]
Desaire, Heather
[1
]
机构:
[1] Univ Kansas, Dept Chem, Lawrence, KS 66045 USA
[2] Duke Univ, Med Ctr, Duke Human Vaccine Inst, Durham, NC USA
关键词:
Glycosylation;
PNGase F;
Endoglycosidase;
HIV;
Envelope protein;
Glycosylation site;
HUMAN-IMMUNODEFICIENCY-VIRUS;
SITE-SPECIFIC ANALYSIS;
ENZYMATIC DEGLYCOSYLATION;
GLYCOPEPTIDE ANALYSIS;
GLYCOSYLATION SITES;
GLYCOPROTEINS;
IDENTIFICATION;
NEUTRALIZATION;
SURVIVAL;
GLYCANS;
D O I:
10.1016/j.ijms.2010.11.009
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
O56 [分子物理学、原子物理学];
学科分类号:
070203 ;
070304 ;
081704 ;
1406 ;
摘要:
The work presented herein describes the first comprehensive analysis of a partially deglycosylated HIV vaccine candidate envelope protein (Env). The Env, JRFL gp140 Delta CF, with 27 potential glycosylation sites, was partially deglycosylated with PNGase F as part of a strategy to generate a more immunogenic HIV vaccine, and the resulting protein glycosylation was characterized in a unique workflow using two different glycosidases, Endo H and Endo F3. This unique analysis protocol provided for coverage on 26 of the 27 glycosylation sites, and the data showed that the biochemical treatment with PNGase F resulted in a highly heterogeneous glycoprotein product that had been partially deglycosylated at most of the glycosylation sites. The protocols described in this work could be useful for characterizing the glycosylation site occupancy of other native or biochemically deglycosylated proteins. (C) 2010 Elsevier B.V. All rights reserved.
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页码:209 / 216
页数:8
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