Polysialic acid: Biosynthesis, novel functions and applications
| Autor: | Chihiro Sato, Karen J. Colley, Ken Kitajima |
|---|---|
| Rok vydání: | 2014 |
| Předmět: |
Models
Molecular chemistry.chemical_classification biology Polysialic acid Mechanism (biology) Immunogenicity Molecular Sequence Data Biochemistry Sialyltransferases Biosynthetic Pathways Cell biology Immune system chemistry Sialic Acids biology.protein Animals Humans Neural cell adhesion molecule Amino Acid Sequence Glycoprotein Cell adhesion Neural Cell Adhesion Molecules Molecular Biology Neurotrophin |
| Zdroj: | Critical Reviews in Biochemistry and Molecular Biology. 49:498-532 |
| ISSN: | 1549-7798 1040-9238 |
| DOI: | 10.3109/10409238.2014.976606 |
| Popis: | As an anti-adhesive, a reservoir for key biological molecules, and a modulator of signaling, polysialic acid (polySia) is critical for nervous system development and maintenance, promotes cancer metastasis, tissue regeneration and repair, and is implicated in psychiatric diseases. In this review, we focus on the biosynthesis and functions of mammalian polySia, and the use of polySia in therapeutic applications. PolySia modifies a small subset of mammalian glycoproteins, with the neural cell adhesion molecule, NCAM, serving as its major carrier. Studies show that mammalian polysialyltransferases employ a unique recognition mechanism to limit the addition of polySia to a select group of proteins. PolySia has long been considered an anti-adhesive molecule, and its impact on cell adhesion and signaling attributed directly to this property. However, recent studies have shown that polySia specifically binds neurotrophins, growth factors, and neurotransmitters and that this binding depends on chain length. This work highlights the importance of considering polySia quality and quantity, and not simply its presence or absence, as its various roles are explored. The capsular polySia of neuroinvasive bacteria allows these organisms to evade the host immune response. While this "stealth" characteristic has made meningitis vaccine development difficult, it has also made polySia a worthy replacement for polyetheylene glycol in the generation of therapeutic proteins with low immunogenicity and improved circulating half-lives. Bacterial polysialyltransferases are more promiscuous than the protein-specific mammalian enzymes, and new studies suggest that these enzymes have tremendous therapeutic potential, especially for strategies aimed at neural regeneration and tissue repair. |
| Databáze: | OpenAIRE |
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