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Sialic acid O-acetylation: From biosynthesis to roles in health and disease
- Source :
- The Journal of Biological Chemistry, Journal of Biological Chemistry, 297, 1-19, Journal of Biological Chemistry, 297, 2, pp. 1-19, Visser, E A, Moons, S J, Timmermans, S B P E, de Jong, H, Boltje, T J & Büll, C 2021, ' Sialic acid O-acetylation : From biosynthesis to roles in health and disease ', Journal of Biological Chemistry, vol. 297, no. 2, 100906, pp. 1-19 . https://doi.org/10.1016/j.jbc.2021.100906
- Publication Year :
- 2021
-
Abstract
- Sialic acids are nine-carbon sugars that frequently cap glycans at the cell surface in cells of vertebrates as well as cells of certain types of invertebrates and bacteria. The nine-carbon backbone of sialic acids can undergo extensive enzymatic modification in nature and O-acetylation at the C-4/7/8/9 position in particular is widely observed. In recent years, the detection and analysis of O-acetylated sialic acids have advanced, and sialic acid-specific O-acetyltransferases (SOATs) and O-acetylesterases (SIAEs) that add and remove O-acetyl groups, respectively, have been identified and characterized in mammalian cells, invertebrates, bacteria, and viruses. These advances now allow us to draw a more complete picture of the biosynthetic pathway of the diverse O-acetylated sialic acids to drive the generation of genetically and biochemically engineered model cell lines and organisms with altered expression of O-acetylated sialic acids for dissection of their roles in glycoprotein stability, development, and immune recognition, as well as discovery of novel functions. Furthermore, a growing number of studies associate sialic acid O-acetylation with cancer, autoimmunity, and infection, providing rationale for the development of selective probes and inhibitors of SOATs and SIAEs. Here, we discuss the current insights into the biosynthesis and biological functions of O-acetylated sialic acids and review the evidence linking this modification to disease. Furthermore, we discuss emerging strategies for the design, synthesis, and potential application of unnatural Oacetylated sialic acids and inhibitors of SOATs and SIAEs that may enable therapeutic targeting of this versatile sialic acid modification.
- Subjects :
- 0301 basic medicine
SOAT, sialic acid O-acetyl transferase
Biochemistry
GBP, glycan-binding protein
chemistry.chemical_compound
IA/B/C/DV, Influenza A/B/C/D virus
KDN, 2-keto-3-deoxynononic acid
N-Glycolylneuraminic acid
S protein, spike protein
Disease
SIAE, sialic acid O-acetyl esterase
SDAV, sialodacryoadenitis virus
sialic acid O-acetyl transferases (SOATs)
biology
EHEC, enterohemorrhagic Escherichia coli
Glycobiology
BCoV, bovine coronavirus
CMP, cytidine 5′-monophosphate
Acetylation
MERS-CoV, Middle East respiratory syndrome coronavirus
MHV-S, murine hepatitis virus strain S
NA, neuraminidase
CPS, capsular polysaccharides
O-Ac, O-acetyl
Glycan
HE, hemagglutinin esterase protein
O-acetylation
SARS-CoV, severe acute respiratory syndrome coronavirus
Hemagglutinin (influenza)
Synthetic Organic Chemistry
Siglec, sialic acid-binding immunoglobulin-like lectin
03 medical and health sciences
glycan modifications
SDG 3 - Good Health and Well-being
glycobiology
Acetyltransferases
Polysaccharides
Sia, sialic acid
NPL, neuraminic acid pyruvate-lyase
Animals
Humans
Molecular Biology
Ac-CoA, acetyl-coenzyme A
Glycoproteins
030102 biochemistry & molecular biology
MUC, mucin
JBC Reviews
HEF, hemagglutinin esterase fusion protein
SIGLEC
Cell Biology
ALL, acute lymphoblastic leukemia
Neu5Gc, N-glycolylneuraminic acid
N-Acetylneuraminic Acid
CASD1, capsule structure1 domain containing 1
Neu5Ac, N-acetylneuraminic acid
Sialic acid
Biosynthetic Pathways
carbohydrates (lipids)
030104 developmental biology
chemistry
influenza C/D virus
biology.protein
sialic acid O-acetyl esterases (SIAEs)
CMAH, CMP-Neu5Ac hydroxylase
sLex, sialyl-Lewisx antigen
Neuraminidase
N-Acetylneuraminic acid
Carboxylic Ester Hydrolases
sialic acids
HA, hemagglutinin
Subjects
Details
- ISSN :
- 1083351X and 00219258
- Volume :
- 297
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi.dedup.....704561863100cd1be53c62370b397510
- Full Text :
- https://doi.org/10.1016/j.jbc.2021.100906