Exploring Metal-Free Click Reactions: New Frontiers in Glycochemistry and Bioconjugation

dc.contributor.authorRamírez López, Pedro
dc.contributor.authorSuárez Álvarez, José Ramón
dc.contributor.authorFlores Aguilar-Amat, Aída
dc.contributor.authorHernáiz Gómez-Degano, María Josefa
dc.date.accessioned2025-07-29T07:40:57Z
dc.date.available2025-07-29T07:40:57Z
dc.date.issued2025
dc.descriptionThe authors gratefully acknowledge financial support provided by the Spanish Ministerio de Economía y Competitividad, Grants TED2021-130430B-C21, PDC2022-133817-I00 and PID2023-150195OB-I00.
dc.description.abstractEfficient and biocompatible methods for synthesizing glycoconjugates are essential in chemical biology, as these molecules play pivotal roles in cellular recognition, signaling, and immune responses. Abnormal glycosylation is associated with diseases such as cancer, infections, and immune disorders, positioning glycoconjugates as promising candidates for therapeutic, diagnostic, and drug delivery applications. Traditional chemical approaches often lack biocompatibility and efficiency; however, the advent of metal-free click chemistry has revolutionized glycoconjugate synthesis by providing selective and versatile tools under mild conditions. This review highlights four remarkable metal-free click reactions: thiol−ene coupling (TEC), strain-promoted azide−alkyne cycloaddition (SPAAC), inverse electron-demand Diels−Alder (IEDDA) reaction, and sulfur fluoride exchange (SuFEx). TEC enables the regio- and stereoselective synthesis of glycoconjugates, including S-polysaccharides, glycopeptides, and glycoclusters, advancing vaccine development and carbohydrate-based therapeutics. SPAAC, a bioorthogonal and metal-free alternative, facilitates in vivo imaging, glycan monitoring, the synthesis of glycofullerenes and glycovaccines, and the development of targeted protein degradation systems such as lysosome-targeting chimeras (LYTACs). Additionally, the combination of SPAAC with biocatalysis offers a sustainable approach for preparing glycoconjugates with therapeutic potential. The IEDDA reaction, a highly efficient metal-free bioorthogonal cycloaddition, plays a key role in metabolic glycoengineering for live-cell imaging and glycan-based therapies and also contributes to the creation of injectable hydrogels for drug delivery and tissue engineering. SuFEx, a more recent reaction, enables efficient sulfonamide and sulfonate bond formation, broadening the toolbox for glycoconjugate and protein functionalization. These methodologies are transforming glycochemistry and glycobiology, driving advancements in biomedicine, materials science, and pharmaceutical development.
dc.description.departmentDepto. de Química en Ciencias Farmacéuticas
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (España)
dc.description.statuspub
dc.identifier.citationPedro Ramírez-López, José Ramón Suárez, Aida Flores, and María J. Hernáiz Bioconjugate Chemistry Article ASAP
dc.identifier.doi10.1021/acs.bioconjchem.5c00049
dc.identifier.officialurlhttps://doi.org/10.1021/acs.bioconjchem.5c00049
dc.identifier.urihttps://hdl.handle.net/20.500.14352/122833
dc.journal.titleBioconjugate Chemistry
dc.language.isoeng
dc.publisherACS Publications
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PDC2022-133817-I00/ES/BIOPRODUCION DE BIOSURFACTANTES CON APLICACION EN LA INDUSTRIA COSMETICA Y FARMACEUTICA: APROXIMACION SOSTENIBLE/
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2023-150195OB-I00/ES/DESARROLLO DE GLICOCONJUGADOS A MEDIDA CONTRA INFECCIONES BACTERIANAS Y VIRICAS/
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu577.1
dc.subject.cdu612.015
dc.subject.cdu615:54
dc.subject.cdu615.31
dc.subject.keywordAddition Reactions
dc.subject.keywordCarbohydrates
dc.subject.keywordChemical Biology
dc.subject.keywordThiols
dc.subject.ucmCiencias
dc.subject.ucmCiencias Biomédicas
dc.subject.ucmQuímica
dc.subject.ucmQuímica orgánica (Química)
dc.subject.ucmQuímica farmaceútica
dc.subject.ucmFarmacia
dc.subject.ucmBiología
dc.subject.unesco23 Química
dc.subject.unesco24 Ciencias de la Vida
dc.subject.unesco2401 Biología Animal (Zoología)
dc.subject.unesco2410 Biología Humana
dc.subject.unesco2403 Bioquímica
dc.subject.unesco2390 Química Farmacéutica
dc.subject.unesco2412 Inmunología
dc.titleExploring Metal-Free Click Reactions: New Frontiers in Glycochemistry and Bioconjugation
dc.typereview article
dc.type.hasVersionVoR
dspace.entity.typePublication
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