A Useful Guide to Lectin Binding: Machine-Learning Directed Annotation of 57 Unique Lectin Specificities.


Journal

ACS chemical biology
ISSN: 1554-8937
Titre abrégé: ACS Chem Biol
Pays: United States
ID NLM: 101282906

Informations de publication

Date de publication:
18 11 2022
Historique:
pubmed: 28 1 2022
medline: 22 11 2022
entrez: 27 1 2022
Statut: ppublish

Résumé

Glycans are critical to every facet of biology and medicine, from viral infections to embryogenesis. Tools to study glycans are rapidly evolving; however, the majority of our knowledge is deeply dependent on binding by glycan binding proteins (e.g., lectins). The specificities of lectins, which are often naturally isolated proteins, have not been well-defined, making it difficult to leverage their full potential for glycan analysis. Herein, we use a combination of machine learning algorithms and expert annotation to define lectin specificity for this important probe set. Our analysis uses comprehensive glycan microarray analysis of commercially available lectins we obtained using version 5.0 of the Consortium for Functional Glycomics glycan microarray (CFGv5). This data set was made public in 2011. We report the creation of this data set and its use in large-scale evaluation of lectin-glycan binding behaviors. Our motif analysis was performed by integrating 68 manually defined glycan features with systematic probing of computational rules for significant binding motifs using mono- and disaccharides and linkages. Combining machine learning with manual annotation, we create a detailed interpretation of glycan-binding specificity for 57 unique lectins, categorized by their major binding motifs: mannose, complex-type

Identifiants

pubmed: 35084820
doi: 10.1021/acschembio.1c00689
pmc: PMC9679999
doi:

Substances chimiques

Lectins 0
Fucose 28RYY2IV3F
Polysaccharides 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2993-3012

Subventions

Organisme : NIAID NIH HHS
ID : 75N93019C00052
Pays : United States
Organisme : NIGMS NIH HHS
ID : P41 GM103694
Pays : United States
Organisme : NIGMS NIH HHS
ID : R24 GM137763
Pays : United States
Organisme : NIGMS NIH HHS
ID : U54 GM062116
Pays : United States

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Auteurs

Daniel Bojar (D)

Department of Chemistry and Molecular Biology and Wallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, Gothenburg, Sweden 405 30.

Lawrence Meche (L)

Biomedical Chemistry Institute, Department of Chemistry, New York University, 100 Washington Square East, Room 1001, New York, New York 10003, United States.

Guanmin Meng (G)

Department of Chemistry, University of Alberta, Edmonton, Canada, T6G 2G2.

William Eng (W)

Biomedical Chemistry Institute, Department of Chemistry, New York University, 100 Washington Square East, Room 1001, New York, New York 10003, United States.

David F Smith (DF)

Department of Biochemistry, Glycomics Center, School of Medicine, Emory University, Atlanta, Georgia 30322, United States.

Richard D Cummings (RD)

Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, United States.

Lara K Mahal (LK)

Biomedical Chemistry Institute, Department of Chemistry, New York University, 100 Washington Square East, Room 1001, New York, New York 10003, United States.
Department of Chemistry, University of Alberta, Edmonton, Canada, T6G 2G2.

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