Glycobiology Protocols

Glycobiology Protocols by Inka Brockhausen, published by Humana Press on September 15, 2006, is a comprehensive resource that delves into the interdisciplinary field of glycobiology, focusing on complex carbohydrates and the post-translational modifications of proteins. This edition spans 382 pages and is presented in English, offering a detailed overview of the evolution of glycobiology from structural elucidation to functional identification of carbohydrates in health and disease.
Readers will find a collection of protocols that provide a solid foundation for investigating glycan functions, emphasizing the complexity of glycosylation processes and the various factors influencing enzyme activity. The book addresses the significance of glycosyltransferases and the intricate dynamics of glycosylation within cells, highlighting the need for further research into how these processes respond to biological and pathological stimuli. Glycobiology Protocols serves as a valuable reference for those engaged in the life sciences, biochemistry, and biophysics, contributing to a deeper understanding of carbohydrate functions in biological systems.
Official synopsis Publisher
Glycobiology involves studies of complex carbohydrates and posttrans- tional modifications of proteins, and has become an important interdiscip- nary field encompassing chemistry, biochemistry, biology, physiology, and pathology. Although initial research was directed toward elucidation of the different carbohydrate structures and the enzymes synthesizing them, the field has now moved toward identifying the functions of carbohydrates. The pro- cols described in Glycobiology Protocols form a solid basis for investigations of glycan functions in health and disease. The cloning of many of the genes participating in glycosylation processes has helped to enhance our knowledge of how glycosylation is controlled, but has also added another dimension of complexity to the great heterogeneous variety of the structures of the oligos- charides of glycoproteins, proteoglycans, and glycolipids. A family of similar enzyme proteins exists for each glycosylation step. Glycosyltransferases are extremely specific for both the nucleotide sugar donor and the acceptor s- strate, but many other factors control sugar transfer, including the locali- tion and topology of enzymes, cofactors, possible chaperone proteins, and the availability of sugar acceptor substrates. The analysis of the intracellular organization of glycosylation and of the factors controlling the activities of the participating enzymes in the cell are important areas that need more research efforts. Another challenge for future research is to understand the glycodynamics of a cell, that is, how the cell responds to stimuli leading to biological and pathological changes in terms of alterations in glycosylation, and how this affects the biology of the cell.
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