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Updated: Feb 16, 2026

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Published on: July 15, 2019
Structure of the chlorovirus PBCV-1 major capsid glycoprotein determined by combining crystallographic and
Cristina De Castro1, Thomas Klose2, Immacolata Speciale3
1Department of Agricultural Sciences, University of Napoli, 80055 Portici, Italy; decastro@unina.it jvanetten1@unl.edu mr@purdue.edu.
Abstract:
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.
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