Structure of the chlorovirus PBCV-1 major capsid glycoprotein determined by combining crystallographic and carbohydrate molecular modeling approaches

被引:28
作者
De Castro, Cristina [1 ]
Klose, Thomas [2 ]
Speciale, Immacolata [3 ]
Lanzetta, Rosa [3 ]
Molinaro, Antonio [3 ]
Van Etten, James L. [4 ,5 ]
Rossmann, Michael G. [2 ]
机构
[1] Univ Napoli, Dept Agr Sci, I-80055 Portici, Italy
[2] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
[3] Univ Napoli, Dept Chem Sci, I-80126 Naples, Italy
[4] Univ Nebraska, Dept Plant Pathol, Lincoln, NE 68583 USA
[5] Univ Nebraska, Nebraska Ctr Virol, Lincoln, NE 68583 USA
基金
美国国家科学基金会;
关键词
virus PBCV-1; capsid protein; N-glycans; glycoprotein structure; chloroviruses; VIRUS; GLYCOSYLATION; PROTEIN; OLIGOSACCHARIDES; NMR;
D O I
10.1073/pnas.1613432115
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 glycans of the major capsid protein (Vp54) of Paramecium bursaria chlorella virus (PBCV-1) were recently described and found to be unusual. This prompted a reexamination of the previously reported Vp54 X-ray structure. A detailed description of the complete glycoprotein was achieved by combining crystallographic data with molecular modeling. The crystallographic data identified most of the monosaccharides located close to the protein backbone, but failed to detect those further from the glycosylation sites. Molecular modeling complemented this model by adding the missing monosaccharides and examined the conformational preference of the whole molecule, alone or within the crystallographic environment. Thus, combining X-ray crystallography with carbohydrate molecular modeling resulted in determining the complete glycosylated structure of a glycoprotein. In this case, it is the chlorovirus PBCV-1 major capsid protein.
引用
收藏
页码:E44 / E52
页数:9
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