Chemical and biological methods for probing the structure and functions of polysialic acids

Abstract

Owing to its poly-anionic charge and large hydrodynamic volume, polysialic acid (polySia) attached to neural cell adhesion molecule regulates axon–axon and axon–substratum interactions and signalling, particularly, in the development of the central nervous system (CNS). Expression of polySia is spatiotemporally regulated by the action of two polysialyl transferases, namely ST8SiaII and ST8SiaIV. PolySia expression peaks during late embryonic and early post-natal period and maintained at a steady state in adulthood in neurogenic niche of the brain. Aberrant polySia expression is associated with neurological disorders and brain tumours. Investigations on the structure and functions, over the past four decades, have shed light on the physiology of polySia. This review focuses on the biological, biochemical, and chemical tools available for polySia engineering. Genetic knockouts, endo-neuraminidases that cleave polySia, antibodies, exogenous expression, and neuroblastoma cells have provided deep insights into the ability of polySia to guide migration of neuronal precursors in neonatal brain development, neuronal clustering, axonal pathway guidance, and axonal targeting. Advent of metabolic sialic acid engineering using ManNAc analogues has enabled reversible and dose-dependent modulation polySia in vitro and ex vivo. In vivo, ManNAc analogues readily engineer the sialoglycans in peripheral tissues, but show no effect in the brain. A recently developed carbohydrate-neuroactive hybrid strategy enables a non-invasive access to the brain in living animals across the blood–brain barrier. A combination of recent advances in CNS drugs and imaging with ManNAc analogues for polySia modulation would pave novel avenues for understanding intricacies of brain development and tackling the challenges of neurological disorders.

Polysialic Acid in the Immune System

“…Unlike a2,3and a2,6-sialylated glycans, which have been easily screened in human cells using lectin panels that use Siabinding lectins such as Maackia amurensis (MAA II; Siaa2,3) and Sambucus nigra (SNA; Siaa2,6) and that have been widely used to determine immune glycophenotypes, no lectins are available to detect polySia (79,80). Additionally, because of its hydrodynamic arrangement, polySia has been difficult to structurally characterize (81). These challenges have lagged the identification of polySia in other tissues; nonetheless, anti-polySia antibodies with differential specificity for the DP are available, easily allowing the identification of polySia (82).…”