Profiling Substrate Promiscuity of Wild-Type Sugar Kinases for Multi-fluorinated Monosaccharides. Issue 9 (17th September 2020)
- Record Type:
- Journal Article
- Title:
- Profiling Substrate Promiscuity of Wild-Type Sugar Kinases for Multi-fluorinated Monosaccharides. Issue 9 (17th September 2020)
- Main Title:
- Profiling Substrate Promiscuity of Wild-Type Sugar Kinases for Multi-fluorinated Monosaccharides
- Authors:
- Keenan, Tessa
Parmeggiani, Fabio
Malassis, Julien
Fontenelle, Clement Q.
Vendeville, Jean-Baptiste
Offen, Wendy
Both, Peter
Huang, Kun
Marchesi, Andrea
Heyam, Alex
Young, Carl
Charnock, Simon J.
Davies, Gideon J.
Linclau, Bruno
Flitsch, Sabine L.
Fascione, Martin A. - Abstract:
- Summary: Fluorinated sugar-1-phosphates are of emerging importance as intermediates in the chemical and biocatalytic synthesis of modified oligosaccharides, as well as probes for chemical biology. Here we present a systematic study of the activity of a wide range of anomeric sugar kinases (galacto- and N -acetylhexosamine kinases) against a panel of fluorinated monosaccharides, leading to the first examples of polyfluorinated substrates accepted by this class of enzymes. We have discovered four new N -acetylhexosamine kinases with a different substrate scope, thus expanding the number of homologs available in this subclass of kinases. Lastly, we have solved the crystal structure of a galactokinase in complex with 2-deoxy-2-fluorogalactose, giving insight into changes in the active site that may account for the specificity of the enzyme toward certain substrate analogs. Graphical Abstract: Highlights: Anomeric kinases screened for activity against fluorinated monosaccharides Phosphorylation of 11 substrates including di- and tetrafluorinated sugars were observed Crystal structure of BiGalK shows active-site interactions with 2FGal This work has practical applications in medicinal chemistry and chemical biology Abstract : Keenan, Parmeggiani et al. report the exploitation of wild-type anomeric sugar kinases to access fluorinated monosaccharide-1-phosphates. They demonstrate the effective phosphorylation of 11 different fluorinated monosaccharides, including di- andSummary: Fluorinated sugar-1-phosphates are of emerging importance as intermediates in the chemical and biocatalytic synthesis of modified oligosaccharides, as well as probes for chemical biology. Here we present a systematic study of the activity of a wide range of anomeric sugar kinases (galacto- and N -acetylhexosamine kinases) against a panel of fluorinated monosaccharides, leading to the first examples of polyfluorinated substrates accepted by this class of enzymes. We have discovered four new N -acetylhexosamine kinases with a different substrate scope, thus expanding the number of homologs available in this subclass of kinases. Lastly, we have solved the crystal structure of a galactokinase in complex with 2-deoxy-2-fluorogalactose, giving insight into changes in the active site that may account for the specificity of the enzyme toward certain substrate analogs. Graphical Abstract: Highlights: Anomeric kinases screened for activity against fluorinated monosaccharides Phosphorylation of 11 substrates including di- and tetrafluorinated sugars were observed Crystal structure of BiGalK shows active-site interactions with 2FGal This work has practical applications in medicinal chemistry and chemical biology Abstract : Keenan, Parmeggiani et al. report the exploitation of wild-type anomeric sugar kinases to access fluorinated monosaccharide-1-phosphates. They demonstrate the effective phosphorylation of 11 different fluorinated monosaccharides, including di- and tetrafluorinated sugars. This work has practical applications in medicinal chemistry and chemical biology, particularly in the synthesis of fluorinated glycans. … (more)
- Is Part Of:
- Cell chemical biology. Volume 27:Issue 9(2020)
- Journal:
- Cell chemical biology
- Issue:
- Volume 27:Issue 9(2020)
- Issue Display:
- Volume 27, Issue 9 (2020)
- Year:
- 2020
- Volume:
- 27
- Issue:
- 9
- Issue Sort Value:
- 2020-0027-0009-0000
- Page Start:
- 1199
- Page End:
- 1206.e5
- Publication Date:
- 2020-09-17
- Subjects:
- biocatalysis -- kinases -- sugar phosphates -- fluorinated carbohydrates -- oligosaccharides -- glycobiology -- enzyme discovery
Biochemistry -- Periodicals
572.05 - Journal URLs:
- http://www.cell.com/cell-chemical-biology/home ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.chembiol.2020.06.005 ↗
- Languages:
- English
- ISSNs:
- 2451-9456
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.733000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14268.xml