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 O-acetylated sialic acids and inhibitors of SOATs and SIAEs that may enable therapeutic targeting of this versatile sialic acid modification.

Highlights

  • Single or multiple O-acetyl modifications at the C-4/7/8/9 position of sialic acids are frequently found in nature and contribute to the diverse functions and interactions of sialoglycans

  • Many aspects of O-Ac-sialic acid (Sia) biosynthesis and biology remain to be explored, research over the past decades has paved the way for recent technical advances in the study of O-Ac-Sias that will place these versatile molecules more into the focus of biological and medical research

  • In particular the identification of capsule structure1 domain containing 1 (CASD1) and sialic-acidspecific esterase (SIAE) has greatly advanced the understanding of mammalian O-Ac-Sia biosynthesis and drives the generation of genetically engineered cell lines and model organisms with gene knockout/in or chemical modifications that will enable discovering the molecular and cellular functions of these enzymes and O-Ac-Sias

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Summary

Edited by Gerald Hart

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 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. The sialic acid family comprises >80 naturally occurring members that are related to the nonulosonic acids, nine-carbon backbone α-keto sugars that are widely found in nature [5,6,7] Regarding this large diversity, the assembly of sialic acid-carrying glycans (sialoglycans) forms a subclass within the glycome—the sialome [8]. A common natural sialic acid modification is the addition of one or more O-acetyl esters to the hydroxyl groups of sialic acid residues yielding about 20 different naturally occurring OAc-Sias [26].

EstA NanS nd nd
Tissue distribution
Development and cancer
Immune regulation and autoimmunity
Sialoglycan degradation and microbiome interactions
Bacterial and parasite infection
Viral infection
Orthomyxoviridae Coronaviridae
Chemical synthesis and inhibitor development
Inhibitors of the sialic acid acetyl esterase
Findings
Conclusion and prospective
Full Text
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