Combining 3D structure with glycan array data provides insight into the origin of glycan specificity. (3rd August 2016)
- Record Type:
- Journal Article
- Title:
- Combining 3D structure with glycan array data provides insight into the origin of glycan specificity. (3rd August 2016)
- Main Title:
- Combining 3D structure with glycan array data provides insight into the origin of glycan specificity
- Authors:
- Grant, Oliver C
Tessier, Matthew B
Meche, Lawrence
Mahal, Lara K
Foley, Bethany L
Woods, Robert J - Abstract:
- Abstract: Defining how a glycan-binding protein (GBP) specifically selects its cognate glycan from among the ensemble of glycans within the cellular glycome is an area of intense study. Powerful insight into recognition mechanisms can be gained from 3D structures of GBPs complexed to glycans; however, such structures remain difficult to obtain experimentally. Here an automated 3D structure generation technique, called computational carbohydrate grafting, is combined with the wealth of specificity information available from glycan array screening. Integration of the array data with modeling and crystallography allows generation of putative co-complex structures that can be objectively assessed and iteratively altered until a high level of agreement with experiment is achieved. Given an accurate model of the co-complexes, grafting is also able to discern which binding determinants are active when multiple potential determinants are present within a glycan. In some cases, induced fit in the protein or glycan was necessary to explain the observed specificity, while in other examples a revised definition of the minimal binding determinants was required. When applied to a collection of 10 GBP–glycan complexes, for which crystallographic and array data have been reported, grafting provided a structural rationalization for the binding specificity of >90% of 1223 arrayed glycans. A webtool that enables researchers to perform computational carbohydrate grafting is available atAbstract: Defining how a glycan-binding protein (GBP) specifically selects its cognate glycan from among the ensemble of glycans within the cellular glycome is an area of intense study. Powerful insight into recognition mechanisms can be gained from 3D structures of GBPs complexed to glycans; however, such structures remain difficult to obtain experimentally. Here an automated 3D structure generation technique, called computational carbohydrate grafting, is combined with the wealth of specificity information available from glycan array screening. Integration of the array data with modeling and crystallography allows generation of putative co-complex structures that can be objectively assessed and iteratively altered until a high level of agreement with experiment is achieved. Given an accurate model of the co-complexes, grafting is also able to discern which binding determinants are active when multiple potential determinants are present within a glycan. In some cases, induced fit in the protein or glycan was necessary to explain the observed specificity, while in other examples a revised definition of the minimal binding determinants was required. When applied to a collection of 10 GBP–glycan complexes, for which crystallographic and array data have been reported, grafting provided a structural rationalization for the binding specificity of >90% of 1223 arrayed glycans. A webtool that enables researchers to perform computational carbohydrate grafting is available at www.glycam.org/gr (accessed 03 March 2016). … (more)
- Is Part Of:
- Glycobiology. Volume 26:Number 7(2016:Jul.)
- Journal:
- Glycobiology
- Issue:
- Volume 26:Number 7(2016:Jul.)
- Issue Display:
- Volume 26, Issue 7 (2016)
- Year:
- 2016
- Volume:
- 26
- Issue:
- 7
- Issue Sort Value:
- 2016-0026-0007-0000
- Page Start:
- 772
- Page End:
- 783
- Publication Date:
- 2016-08-03
- Subjects:
- binding determinant -- glycan array screening -- glycan-binding protein -- lectin specificity -- 3D structure
Glycoproteins -- Periodicals
Glycolipids -- Periodicals
Glycoconjugates -- Periodicals
572.567 - Journal URLs:
- http://glycob.oupjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/glycob/cww020 ↗
- Languages:
- English
- ISSNs:
- 0959-6658
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4196.303000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24975.xml