Restoring protein glycosylation with GlycoShape

Despite ground-breaking innovations in experimental structural biology and protein structure prediction techniques, capturing the structure of the glycans that functionalize proteins remains a challenge. Here we introduce GlycoShape ( https://glycoshape.org ), an open-access glycan structure database and toolbox designed to restore glycoproteins to their native and functional form in seconds. The GlycoShape database counts over 500 unique glycans so far, covering the human glycome and augmented by elements from a wide range of organisms, obtained from 1 ms of cumulative sampling from molecular dynamics simulations. These structures can be linked to proteins with a robust algorithm named Re-Glyco, directly compatible with structural data in open-access repositories, such as the Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB) and AlphaFold Protein Structure Database, or own. The quality, performance and broad applicability of GlycoShape is demonstrated by its ability to predict N-glycosylation occupancy, scoring a 93% agreement with experiment, based on screening all proteins in the PDB with a corresponding glycoproteomics profile, for a total of 4,259 N-glycosylation sequons.

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Publication Details

Journal
Nature Methods
Published
2024-10-14
DOI
https://doi.org/10.1038/s41592-024-02464-7
Citations
48
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
11.22

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article

Restoring protein glycosylation with GlycoShape

Elisa Fadda, Aoife M. Harbison, Carl A. Fogarty, Ojas Singh et al.
48 citations
Nature Methods
Glycosylation and Glycoproteins Research
11.22
article

Restoring protein glycosylation with GlycoShape

Elisa Fadda, Aoife M. Harbison, Carl A. Fogarty, Ojas Singh, Beatrice Tropea, Callum M. Ives, Akash Satheesan, Silvia D’Andrea
article en
48 citations

Abstract

Despite ground-breaking innovations in experimental structural biology and protein structure prediction techniques, capturing the structure of the glycans that functionalize proteins remains a challenge. Here we introduce GlycoShape ( https://glycoshape.org ), an open-access glycan structure database and toolbox designed to restore glycoproteins to their native and functional form in seconds. The GlycoShape database counts over 500 unique glycans so far, covering the human glycome and augmented by elements from a wide range of organisms, obtained from 1 ms of cumulative sampling from molecular dynamics simulations. These structures can be linked to proteins with a robust algorithm named Re-Glyco, directly compatible with structural data in open-access repositories, such as the Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB) and AlphaFold Protein Structure Database, or own. The quality, performance and broad applicability of GlycoShape is demonstrated by its ability to predict N-glycosylation occupancy, scoring a 93% agreement with experiment, based on screening all proteins in the PDB with a corresponding glycoproteomics profile, for a total of 4,259 N-glycosylation sequons.

Nature MethodsVol. 21(11)
National University of Ireland, Maynooth (IE), University of Southampton (GB)
Cooley's Anemia Foundation, University of Southampton, Science Foundation Ireland, University College Dublin, Irish Research Council, Irish Centre for High-End Computing
Industry, innovation and infrastructure
Openalex Percentile: Top 1%
Glycosylation and Glycoproteins Research
11.22
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