Editorial on the Research Topic
Glyco-Tools to Crack Unsolved Biomedical Needs
The last advances in glycosciences have highlighted the multiple roles of glycans in complex biological systems. We are indeed now in the glycome era which, along with the genome and proteome, is essential for understanding and dissecting the complexity of cells. The improvement of structural and synthetic approaches, including microfluidic and enzymatic strategies, as well as the development of high-throughput glycan microarray technology, give us nowadays a unique opportunity to elucidate the role of glycans in distinct biological contexts (). Recently, glycoconjugate RNA molecules (glycoRNAs) have been identified on cell surface by Flynn et al., adding a new player into the glyco signature atlas (). Glycans are dynamic structures, and their composition and distribution rely on individual’s ages, diseases and diet, making them precious targets for the development of personalized theragnostic strategies. None the less, the involvement of glycans in human health and disease is more complex than we have anticipated, in fact glycans are strongly engaged in cell fate, control, signalling, and extracellular communications. In this perspective, glycoscience represents an enormous inspiration source for the design of advanced diagnostic systems and for the development of biotechnological, new generation of therapeutic treatments.
In this Editorial firefront scientific studies are described showing the multidisciplinary nature of glycoscience. Metabolic glycoengineering (MGE) is one of the most impressive techniques employable to clarify the roles of glycans. MGE has been developed in the late 1980s and today its application is showing terrific impact in both diagnostics and therapeutics (). This topic is reviewed by Haiber et al., with exhaustive examples highlighting electron-demand Diels-Alder bioortogonal reactions as a cell-friendly ligation strategy suitable for healthcare applications.
Lectins are glycan binding proteins (GBP) and one of the main players for the biological relevance of glycans. Lectins are important targets due to their role in cell signalling, cell migration and differentiation or in concerted processes like angiogenesis (). They are mediators of pathological phenomena like cancer, inflammation and infection, playing a fundamental role in the maintenance of physiological conditions or in the unbalanced pathological cascade. Quintana et al. provide new insights on A and B histo blood group antigens binding to Galectin-4 (Gal-4), allowing the identification of interactions and their structure-based rationale thanks to the concerted employment of NMR, isothermal titration calorimetry, and molecular modelling.
Glycans are also active players involved in microbial recognition and infection. Like in mammalians biological pathways, also in microbial populations the interactions between bacteria or viruses and hosts are mediated by carbohydrate–proteins interactions. Marchetti et al. describe the recognition of host sialoglycans by hemagglutinin-neuraminidase isolated from SBL-1 strain of Mumps Viruses by concerted application of NMR, computational studies, and fluorescence assays. They also exploit a N-acetylneuraminic acid-derived thiotrisaccharide to target the viral protein.
Glycomimetics able to act as GBP inhibitors, allow to maximise the information on a large plethora of GBP involved in the maintenance of physiological processes or responsible for pathological phenomena. With this aim Weiss et al. present the synthesis and the evaluation of the activity of molecules able to bind O-GlcNAc transferase, enzyme involved in the transfer of O-GlcNAc to proteins. Thanks to a library of 2-oxo-1,2-dihydroquinoline-4-carboxamide derivatives, and the employment of different evaluation tests, interestingly false positive data obtained from commercial UDP-Glo™ glycosyltransferase assay were highlighted.
Glycans and glycomimetics can be also exploited when conjugated to macromolecular systems or nanomaterials to mimic the known multivalent behaviour of glycoconjugate proteins expressed in mammalian, microbial or vegetable biological systems. Hernando et al. provide a wide overview of carbohydrate-coated nanoparticles, overlying their use in biomedicine, including the detection of proteins or key interactors of viruses and bacteria or cancer cells. Colloidal glyconanoparticles and quantum dot have been taken into consideration, providing insights on the unresolved challenges and the future efforts needed to overcome the current limitations. Further potential applications of glyconanoparticles are reviewed by Kim et al., including the study of the interactions occurring between solid and lipid nanoparticle functionalized with glycans and receptor expressed on cell surfaces.
Polysaccharides expressed at cellular and extracellular level are also employed to develop glycan-based tools for biomedical application. Their physical and biological properties, exploited at extracellular level in tissues and organs, make them perfect scaffolds to maximise the performances of implantable medical devices. Lepedda et al. present a critical analysis of the employment of glycosaminoglycans (GAGs) as signalling molecules able to induce artery formation and, in general, their potential in the development of biomaterials for vascular regeneration.
In conclusion, the research topics collected in this Research Topic perfectly reflect the multifaced expertise which characterizes the glycoscience field and which are fundamental to path the way to future ambitious challenges in biomedical field.
Statements
Author contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
Acknowledgments
The authors thank the COST Action Functional Glyconanomaterials for the Development of Diagnostics and Targeted Therapeutic Probes (CA18132).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1
AgatemorC.BuettnerM. J.ArissR.MuthiahK.SaeuiC. T.YaremaK. J. (2019). Exploiting Metabolic Glycoengineering to Advance Healthcare. Nat. Rev. Chem.3, 605–620. 10.1038/s41570-019-0126-y
2
JohannesL.JacobR.LefflerH. (2018). Galectins at a Glance. J. Cell Sci.131 (9), jcs208884. 10.1242/jcs.208884
3
FlynnR. A.PedramK.MalakerS. A.BatistaP. J.SmithB. A. H.JohnsonA. J.et al (2021). Small RNAs are Modified with N-Glycans and Displayed on the Surface of Living Cells. Cell184 (12), 3109–3124.e22. 10.1016/j.cell.2021.04.023
4
SmithB. A. H.Bertozzi C. R. (2021). The Clinical Impact of Glycobiology: Targeting Selectins, Siglecs and Mammalian Glycans. Nat. Rev. Drug Discov.20 (3), 217–243.
Summary
Keywords
glycans, glycomimetics, glycan binding proteins, glyconanoparticles, glycan protein interactions, glycoprobes, glycotools
Citation
Marcelo F, Nativi C, Russo L, Silipo A and Velasco-Torrijos T (2021) Editorial: Glyco-Tools to Crack Unsolved Biomedical Needs. Front. Chem. 9:789839. doi: 10.3389/fchem.2021.789839
Received
05 October 2021
Accepted
12 October 2021
Published
18 November 2021
Volume
9 - 2021
Edited and reviewed by
John D. Wade, University of Melbourne, Australia
Updates
Copyright
© 2021 Marcelo, Nativi, Russo, Silipo and Velasco-Torrijos.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Laura Russo, laura.russo@unimib.it
This article was submitted to Chemical Biology, a section of the journal Frontiers in Chemistry
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.