Self‐Assembling Proteins as High‐Performance Substrates for Embryonic Stem Cell Self‐Renewal

dc.contributor.authorHill, Christopher J.
dc.contributor.authorFleming, Jennifer R.
dc.contributor.authorMousavinejad, Masoumeh
dc.contributor.authorNicholson, Rachael
dc.contributor.authorTzokov, Svetomir B.
dc.contributor.authorBullough, Per A.
dc.contributor.authorBogomolovas, Julius
dc.contributor.authorMorgan, Mark R.
dc.contributor.authorMayans, Olga
dc.contributor.authorMurray, Patricia
dc.date.accessioned2019-05-22T11:32:20Z
dc.date.available2019-05-22T11:32:20Z
dc.date.issued2019-04eng
dc.description.abstractThe development of extracellular matrix mimetics that imitate niche stem cell microenvironments and support cell growth for technological applications is intensely pursued. Specifically, mimetics are sought that can enact control over the self-renewal and directed differentiation of human pluripotent stem cells (hPSCs) for clinical use. Despite considerable progress in the field, a major impediment to the clinical translation of hPSCs is the difficulty and high cost of large-scale cell production under xeno-free culture conditions using current matrices. Here, a bioactive, recombinant, protein-based polymer, termed ZTFn , is presented that closely mimics human plasma fibronectin and serves as an economical, xeno-free, biodegradable, and functionally adaptable cell substrate. The ZTFn substrate supports with high performance the propagation and long-term self-renewal of human embryonic stem cells while preserving their pluripotency. The ZTFn polymer can, therefore, be proposed as an efficient and affordable replacement for fibronectin in clinical grade cell culturing. Further, it can be postulated that the ZT polymer has significant engineering potential for further orthogonal functionalization in complex cell applications.eng
dc.description.versionpublishedeng
dc.identifier.doi10.1002/adma.201807521eng
dc.identifier.pmid30866118eng
dc.identifier.ppn1677541539
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/45877
dc.language.isoengeng
dc.rightsterms-of-use
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dc.subject.ddc570eng
dc.titleSelf‐Assembling Proteins as High‐Performance Substrates for Embryonic Stem Cell Self‐Renewaleng
dc.typeJOURNAL_ARTICLEeng
dspace.entity.typePublication
kops.citation.bibtex
@article{Hill2019-04SelfA-45877,
  year={2019},
  doi={10.1002/adma.201807521},
  title={Self‐Assembling Proteins as High‐Performance Substrates for Embryonic Stem Cell Self‐Renewal},
  number={17},
  volume={31},
  issn={0935-9648},
  journal={Advanced Materials},
  author={Hill, Christopher J. and Fleming, Jennifer R. and Mousavinejad, Masoumeh and Nicholson, Rachael and Tzokov, Svetomir B. and Bullough, Per A. and Bogomolovas, Julius and Morgan, Mark R. and Mayans, Olga and Murray, Patricia},
  note={Article Number: 1807521}
}
kops.citation.iso690HILL, Christopher J., Jennifer R. FLEMING, Masoumeh MOUSAVINEJAD, Rachael NICHOLSON, Svetomir B. TZOKOV, Per A. BULLOUGH, Julius BOGOMOLOVAS, Mark R. MORGAN, Olga MAYANS, Patricia MURRAY, 2019. Self‐Assembling Proteins as High‐Performance Substrates for Embryonic Stem Cell Self‐Renewal. In: Advanced Materials. 2019, 31(17), 1807521. ISSN 0935-9648. eISSN 1521-4095. Available under: doi: 10.1002/adma.201807521deu
kops.citation.iso690HILL, Christopher J., Jennifer R. FLEMING, Masoumeh MOUSAVINEJAD, Rachael NICHOLSON, Svetomir B. TZOKOV, Per A. BULLOUGH, Julius BOGOMOLOVAS, Mark R. MORGAN, Olga MAYANS, Patricia MURRAY, 2019. Self‐Assembling Proteins as High‐Performance Substrates for Embryonic Stem Cell Self‐Renewal. In: Advanced Materials. 2019, 31(17), 1807521. ISSN 0935-9648. eISSN 1521-4095. Available under: doi: 10.1002/adma.201807521eng
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kops.sourcefieldAdvanced Materials. 2019, <b>31</b>(17), 1807521. ISSN 0935-9648. eISSN 1521-4095. Available under: doi: 10.1002/adma.201807521deu
kops.sourcefield.plainAdvanced Materials. 2019, 31(17), 1807521. ISSN 0935-9648. eISSN 1521-4095. Available under: doi: 10.1002/adma.201807521deu
kops.sourcefield.plainAdvanced Materials. 2019, 31(17), 1807521. ISSN 0935-9648. eISSN 1521-4095. Available under: doi: 10.1002/adma.201807521eng
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