Publication:
Midkine Interaction with Chondroitin Sulfate Model Synthetic Tetrasaccharides and Their Mimetics: The Role of Aromatic Interactions.

dc.contributor.authorGarcía-Jiménez, María José
dc.contributor.authorGil-Caballero, Sergio
dc.contributor.authorMaza, Susana
dc.contributor.authorCorzana, Francisco
dc.contributor.authorJuárez-Vicente, Francisco
dc.contributor.authorMiles, Jonathan R
dc.contributor.authorSakamoto, Kazuma
dc.contributor.authorKadomatsu, Kenji
dc.contributor.authorGarcía-Domínguez, Mario
dc.contributor.authorde Paz, José L
dc.contributor.authorNieto, Pedro M
dc.date.accessioned2023-02-09T11:42:25Z
dc.date.available2023-02-09T11:42:25Z
dc.date.issued2021-07-20
dc.description.abstractMidkine (MK) is a neurotrophic factor that participates in the embryonic central nervous system (CNS) development and neural stem cell regulation, interacting with sulfated glycosaminoglycans (GAGs). Chondroitin sulfate (CS) is the natural ligand in the CNS. In this work, we describe the interactions between a library of synthetic models of CS-types and mimics. We did a structural study of this library by NMR and MD (Molecular Dynamics), concluding that the basic shape is controlled by similar geometry of the glycosidic linkages. Their 3D structures are a helix with four residues per turn, almost linear. We have studied the tetrasaccharide-midkine complexes by ligand observed NMR techniques and concluded that the shape of the ligands does not change upon binding. The ligand orientation into the complex is very variable. It is placed inside the central cavity of MK formed by the two structured beta-sheets domains linked by an intrinsically disordered region (IDR). Docking analysis confirmed the participation of aromatics residues from MK completed with electrostatic interactions. Finally, we test the biological activity by increasing the MK expression using CS tetrasaccharides and their capacity in enhancing the growth stimulation effect of MK in NIH3T3 cells.
dc.identifier.doi10.1002/chem.202101674
dc.identifier.essn1521-3765
dc.identifier.pmcPMC8457220
dc.identifier.pmid34213045
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457220/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1002/chem.202101674
dc.identifier.urihttp://hdl.handle.net/10668/18144
dc.issue.number48
dc.journal.titleChemistry (Weinheim an der Bergstrasse, Germany)
dc.journal.titleabbreviationChemistry
dc.language.isoen
dc.organizationCentro Andaluz de Biología Molecular y Medicina Regenerativa-CABIMER
dc.page.number12395-12409
dc.pubmedtypeJournal Article
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectMD
dc.subjectSTD NMR spectroscopy
dc.subjectcarbohydrate-protein complexes
dc.subjectchondroitin sulfate
dc.subjectmidkine
dc.subjecttransient NMRspectroscopy
dc.subject.meshAnimals
dc.subject.meshChondroitin Sulfates
dc.subject.meshGlycosaminoglycans
dc.subject.meshMice
dc.subject.meshMidkine
dc.subject.meshNIH 3T3 Cells
dc.subject.meshOligosaccharides
dc.titleMidkine Interaction with Chondroitin Sulfate Model Synthetic Tetrasaccharides and Their Mimetics: The Role of Aromatic Interactions.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number27
dspace.entity.typePublication

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