Εμφάνιση απλής εγγραφής

dc.creatorSarri C.A., Giannoulis T., Moutou K.A., Mamuris Z.en
dc.date.accessioned2023-01-31T09:54:03Z
dc.date.available2023-01-31T09:54:03Z
dc.date.issued2021
dc.identifier10.1016/j.imlet.2021.07.005
dc.identifier.issn01652478
dc.identifier.urihttp://hdl.handle.net/11615/78799
dc.description.abstractBackground: HLA-class II proteins hold important roles in key physiological processes. The purpose of this study was to compile all class II alleles reported in human population and investigate patterns in pocket variants and their combinations, focusing on the peptide-binding region (PBR). Methods: For this purpose, all protein sequences of DPA1, DQA1, DPB1, DQB1 and DRB1 were selected and filtered, in order to have full PBR sequences. Proportional representation was used for pocket variants while population data were also used. Results: All pocket variants and PBR sequences were retrieved and analyzed based on the preference of amino acids and their properties in all pocket positions. The observed number of pocket variants combinations was much lower than the possible inferred, suggesting that PBR formation is under strict funneling. Also, although class II proteins are very polymorphic, in the majority of the reported alleles in all populations, a significantly less polymorphic pocket core was found. Conclusions: Pocket variability of five HLA class II proteins was studied revealing favorable properties of each protein. The actual PBR sequences of HLA class II proteins appear to be governed by restrictions that lead to the establishment of only a fraction of the possible combinations and the polymorphism recorded is the result of intense funneling based on function. © 2021 European Federation of Immunological Societiesen
dc.language.isoenen
dc.sourceImmunology Lettersen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85112704457&doi=10.1016%2fj.imlet.2021.07.005&partnerID=40&md5=47d7f7dd956bc27b173344f3b32a2ff2
dc.subjectamino aciden
dc.subjectDPA1 proteinen
dc.subjectHLA antigen class 2en
dc.subjectHLA DPA1 antigenen
dc.subjectHLA DPB1 antigenen
dc.subjectHLA DQA1 antigenen
dc.subjectHLA DQB1 antigenen
dc.subjectHLA DRB1 antigenen
dc.subjectunclassified drugen
dc.subjectHLA antigen class 2en
dc.subjectHLA DQ antigenen
dc.subjectpeptideen
dc.subjectalleleen
dc.subjectamino acid sequenceen
dc.subjectArticleen
dc.subjectbinding siteen
dc.subjectcontrolled studyen
dc.subjectfractionationen
dc.subjectfunneling activityen
dc.subjecthumanen
dc.subjectphysical chemistryen
dc.subjectprotein bindingen
dc.subjectprotein functionen
dc.subjectsingle nucleotide polymorphismen
dc.subjectchemistryen
dc.subjectgenetic polymorphismen
dc.subjectgeneticsen
dc.subjectimmunologyen
dc.subjectnucleotide sequenceen
dc.subjectprotein motifen
dc.subjectAllelesen
dc.subjectAmino Acid Motifsen
dc.subjectAmino Acid Sequenceen
dc.subjectBase Sequenceen
dc.subjectBinding Sitesen
dc.subjectHistocompatibility Antigens Class IIen
dc.subjectHLA-DQ beta-Chainsen
dc.subjectHumansen
dc.subjectPeptidesen
dc.subjectPolymorphism, Geneticen
dc.subjectElsevier B.V.en
dc.titleHLA class II peptide-binding-region analysis reveals funneling of polymorphism in actionen
dc.typejournalArticleen


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