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dc.contributor.authorLareu, Ricky R.
dc.contributor.authorSubramhanya, H.
dc.contributor.authorPeng, Y.
dc.contributor.authorBenny, P.
dc.contributor.authorChen, C.
dc.contributor.authorWang, Z.
dc.contributor.authorRajagopalan, R.
dc.contributor.authorRaghunath, M.
dc.date.accessioned2017-01-30T13:26:16Z
dc.date.available2017-01-30T13:26:16Z
dc.date.created2014-02-25T20:00:39Z
dc.date.issued2007
dc.identifier.citationLareu, Ricky R. and Subramhanya, Karthik Harve and Peng, Yanxian and Benny, Paula and Chen, Clarice and Wang, Zhibo and Rajagopalan, Raj and Raghunath, Michael. 2007. Collagen matrix deposition is dramatically enhanced in vitro when crowded with charged macromolecules: The biological relevance of the excluded volume effect. FEBS Letters. 581 (14): pp. 2709-2714.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/31588
dc.identifier.doi10.1016/j.febslet.2007.05.020
dc.description.abstract

The excluded volume effect (EVE) rules all life processes. It is created by macromolecules that occupy a given volume thereby confining other molecules to the remaining space with large consequences on reaction kinetics and molecular assembly. Implementing EVE in fibroblast culture accelerated conversion of procollagen to collagen by procollagen C-proteinase (PCP/BMP-1) and proteolytic modification of its allosteric regulator, PCOLCE1. This led to a 20–30- and 3–6-fold increased collagen deposition in two- and three-dimensional cultures, respectively, and creation of crosslinked collagen footprints beneath cells. Important parameters correlating with accelerated deposition were hydrodynamic radius of macromolecules and their negative charge density.

dc.publisherElsevier Science BV
dc.subjectMacromolecular crowding
dc.subjectExtracellular matrix
dc.subjectProcollagen C-proteinase
dc.subjectExcluded volume effect
dc.subjectCollagen deposition
dc.titleCollagen matrix deposition is dramatically enhanced in vitro when crowded with charged macromolecules: The biological relevance of the excluded volume effect
dc.typeJournal Article
dcterms.source.volume581
dcterms.source.number14
dcterms.source.startPage2709
dcterms.source.endPage2714
dcterms.source.issn0014-5793
dcterms.source.titleFEBS Letters
curtin.department
curtin.accessStatusOpen access via publisher


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