Over the last decade the fields of glycobiology and glycochemistry in combination with in-silico applications have been augmented by a further field - glycomics. A major aim of glycomics research is to achieve a comprehensive identification and characterization of the repertoire of glycan structures present in an organism, cell or tissue at a defined time. In addition, glycans and glycoconjugates have been increasingly perceived by the proteomics and genomics communities as essential elements in physiological and pathological processes rather than as decorative elements of lipids and proteins.
Glycans are extremely complex and diverse in their structures and thus it has been necessary to develop a wide range of experimental techniques and instrumentation for their detection and analysis. With the advancement of techniques for the interactive and structural analysis of glycoconjugates their essential role in phenomena such as cell adherence, cell–cell interactions, molecular trafficking, biosynthetic quality control, signal transduction and host– pathogen recognition, became apparent. Much efforts have been spent into describing both the structure and binding of glycans and these investigations also resulted in the observation of patterns of glycosylation which change in dependence of the developmental status of the cells. This makes glycosylation patterns an important marker for the detection of diseases and cellular malfunction. However, exciting questions are still unanswered that include the way of “encoding” and control of these diverse patterns and structure-function relationships of the vast variety of glycan structures and patterns. First milestones have been reached towards deciphering the purpose of glycan structures by applying a combination of experimental and bioinformatics tools.