Hydroxylated oxanes as xyloside analogs for determination of the minimal binding requirements of β4GalT7
(2017) In Tetrahedron Letters 58(35). p.3466-3469- Abstract
β-1,4-Galactosyltransferase 7 (β4GalT7) is a key enzyme in the biosynthesis of glycosaminoglycan (GAG) chains. Natural and synthetic xylosides can be used to both inhibit and prime GAG synthesis by acting as inhibitors or substrates for β4GalT7. In this report, we exploit hydroxylated oxanes as deoxygenated xyloside analogs to clarify the minimum protein-ligand interactions required for galactosylation and/or inhibition. Enantiomerically pure substances were synthesized using a chiral pool approach whereas the corresponding racemates were obtained from simple starting materials. The results of a β4GalT7 assay show that a single hydroxyl group on an oxane ring is insufficient to induce galactosylation or inhibition, which implies that at... (More)
β-1,4-Galactosyltransferase 7 (β4GalT7) is a key enzyme in the biosynthesis of glycosaminoglycan (GAG) chains. Natural and synthetic xylosides can be used to both inhibit and prime GAG synthesis by acting as inhibitors or substrates for β4GalT7. In this report, we exploit hydroxylated oxanes as deoxygenated xyloside analogs to clarify the minimum protein-ligand interactions required for galactosylation and/or inhibition. Enantiomerically pure substances were synthesized using a chiral pool approach whereas the corresponding racemates were obtained from simple starting materials. The results of a β4GalT7 assay show that a single hydroxyl group on an oxane ring is insufficient to induce galactosylation or inhibition, which implies that at least two substituents, one of which being 3-OH, needs to be present.
(Less)
- author
- Thorsheim, Karin
LU
; Clementson, Sebastian
; Tykesson, Emil
LU
; Strand, Daniel LU ; Ellervik, Ulf LU
and Bengtsson, Dennis
- organization
- publishing date
- 2017-08-30
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Chiral pool approach, De novo synthesis, Mechanistic probes, Xyloside analogs, β4GalT7
- in
- Tetrahedron Letters
- volume
- 58
- issue
- 35
- pages
- 4 pages
- publisher
- Elsevier
- external identifiers
-
- scopus:85026414813
- ISSN
- 0040-4039
- DOI
- 10.1016/j.tetlet.2017.07.078
- language
- English
- LU publication?
- yes
- id
- db7ce79e-fc0a-46f9-8df3-dc4eebf26eb3
- date added to LUP
- 2017-08-29 12:47:35
- date last changed
- 2025-04-04 15:17:41
@article{db7ce79e-fc0a-46f9-8df3-dc4eebf26eb3, abstract = {{<p>β-1,4-Galactosyltransferase 7 (β4GalT7) is a key enzyme in the biosynthesis of glycosaminoglycan (GAG) chains. Natural and synthetic xylosides can be used to both inhibit and prime GAG synthesis by acting as inhibitors or substrates for β4GalT7. In this report, we exploit hydroxylated oxanes as deoxygenated xyloside analogs to clarify the minimum protein-ligand interactions required for galactosylation and/or inhibition. Enantiomerically pure substances were synthesized using a chiral pool approach whereas the corresponding racemates were obtained from simple starting materials. The results of a β4GalT7 assay show that a single hydroxyl group on an oxane ring is insufficient to induce galactosylation or inhibition, which implies that at least two substituents, one of which being 3-OH, needs to be present.</p>}}, author = {{Thorsheim, Karin and Clementson, Sebastian and Tykesson, Emil and Strand, Daniel and Ellervik, Ulf and Bengtsson, Dennis}}, issn = {{0040-4039}}, keywords = {{Chiral pool approach; De novo synthesis; Mechanistic probes; Xyloside analogs; β4GalT7}}, language = {{eng}}, month = {{08}}, number = {{35}}, pages = {{3466--3469}}, publisher = {{Elsevier}}, series = {{Tetrahedron Letters}}, title = {{Hydroxylated oxanes as xyloside analogs for determination of the minimal binding requirements of β4GalT7}}, url = {{http://dx.doi.org/10.1016/j.tetlet.2017.07.078}}, doi = {{10.1016/j.tetlet.2017.07.078}}, volume = {{58}}, year = {{2017}}, }