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Spermine Sepharose as a clustered-charge anion exchange adsorbent

dc.contributor.authorRuiz Ruiz, Fernando
dc.contributor.authorDhamanea, Sagar
dc.contributor.authorChen, Wen-Hsiang
dc.contributor.authorKourentzic, Katerina
dc.contributor.authorBenavides, Jorge
dc.contributor.authorRito Palomares, Marco
dc.contributor.authorWillson, Richard C.
dc.date.accessioned2023-06-19T13:24:07Z
dc.date.available2023-06-19T13:24:07Z
dc.date.issued2014-01-10
dc.description© 2013 Elsevier B.V. All rights reserved. This research was funded by the Robert A. Welch foundation under Grant E-1264 and the National Science Foundation (NSF) Division of Chemical, Bioengineering, Environmental, and Transport Systems (CBET-1133965). The authors also acknowledge Tecnológico de Monterrey Research chair (Grant CAT161) and CONACyT for fellowship #295368 to FRR.
dc.description.abstractWe previously showed that the affinity and capacity of ion exchange adsorbents of a given total charge density are improved by immobilization of the charges in pre-ordered clusters, rather than individually in random locations. This previous work used pentalysinamide and pentaargininamide as clustered ligands. This approach allows close control of cluster size, but is uneconomically expensive for some research and most practical applications. In this work, we demonstrate that the inexpensive synthetic analog of the natural polyamine spermine (H2N-CH2-CH2-CH2-NH-CH2-CH2-CH2-CH2-NH-CH2-CH2-CH2 NH2) also can serve as the basis of effective clustered adsorbents. The calcium-depleted form of the protein a lactalbumin, and RNA from baker's yeast, were adsorbed on a spermine Sepharose adsorbent. This adsorbent exhibited enhanced alpha lactalbumin binding capacity (Q(max) >1.6 and 1.3-fold higher than those for Qiagen DEAE and GE DEAE Sepharose adsorbents of much greater charge density) and higher initial binding affinity (Q(max)/K-D 2.4 and 2.1 fold higher, respectively). The new spermine-based matrix exhibited a higher value of the Z parameter, suggesting an increased number of apparent interaction sites between the protein and the resin, and functioned well in column mode. (C) 2013 Elsevier B.V. All rights reserved.
dc.description.departmentDepto. de Física Teórica
dc.description.facultyFac. de Ciencias Físicas
dc.description.refereedTRUE
dc.description.sponsorshipRobert A. Welch foundation
dc.description.sponsorshipNational Science Foundation (NSF)
dc.description.sponsorshipCONACyT
dc.description.sponsorshipTecnológico de Monterrey
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/25545
dc.identifier.doi10.1016/j.chroma.2013.11.030
dc.identifier.issn0021-9673
dc.identifier.officialurlhttp://dx.doi.org/10.1016/j.chroma.2013.11.030
dc.identifier.relatedurlhttp://www.sciencedirect.com
dc.identifier.urihttps://hdl.handle.net/20.500.14352/33548
dc.journal.titleJournal of Chromatography A
dc.language.isoeng
dc.page.final140
dc.page.initial135
dc.publisherElsevier Science Bv
dc.relation.projectIDE-1264
dc.relation.projectIDCBET-1133965
dc.relation.projectID#295368
dc.relation.projectIDCAT161
dc.rights.accessRightsopen access
dc.subject.cdu53
dc.subject.keywordThermodynamic Driving Forces
dc.subject.keywordBovine Alpha-Lactalbumin
dc.subject.keywordIon-Exchange
dc.subject.keywordLigand Density
dc.subject.keywordCytochrome B(5)
dc.subject.keywordMolten-Globule
dc.subject.keywordCompact State
dc.subject.keywordChromatography
dc.subject.keywordProteins
dc.subject.keywordAdsorption
dc.subject.ucmFísica (Física)
dc.subject.unesco22 Física
dc.titleSpermine Sepharose as a clustered-charge anion exchange adsorbent
dc.typejournal article
dc.volume.number1324
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