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dc.contributor.authorRojas, Fredrick P.
dc.contributor.authorBatista, Michael A.
dc.contributor.authorLindburg, C. Alexander
dc.contributor.authorDean, Delphine
dc.contributor.authorGrodzinsky, Alan J.
dc.contributor.authorOrtiz, Christine
dc.contributor.authorHan, Lin
dc.date.accessioned2015-04-22T15:33:47Z
dc.date.available2015-04-22T15:33:47Z
dc.date.issued2014-03
dc.date.submitted2014-01
dc.identifier.issn1525-7797
dc.identifier.issn1526-4602
dc.identifier.urihttp://hdl.handle.net/1721.1/96694
dc.description.abstractIn this study, we investigated the molecular adhesion between the major constituents of cartilage extracellular matrix, namely, the highly negatively charged proteoglycan aggrecan and the type II/IX/XI fibrillar collagen network, in simulated physiological conditions. Colloidal force spectroscopy was applied to measure the maximum adhesion force and total adhesion energy between aggrecan end-attached spherical tips (end radius R ≈ 2.5 μm) and trypsin-treated cartilage disks with undamaged collagen networks. Studies were carried out in various aqueous solutions to reveal the physical factors that govern aggrecan–collagen adhesion. Increasing both ionic strength and [Ca2+] significantly increased adhesion, highlighting the importance of electrostatic repulsion and Ca2+-mediated ion bridging effects. In addition, we probed how partial enzymatic degradation of the collagen network, which simulates osteoarthritic conditions, affects the aggrecan–collagen interactions. Interestingly, we found a significant increase in aggrecan–collagen adhesion even when there were no detectable changes at the macro- or microscales. It is hypothesized that the aggrecan–collagen adhesion, together with aggrecan–aggrecan self-adhesion, works synergistically to determine the local molecular deformability and energy dissipation of the cartilage matrix, in turn, affecting its macroscopic tissue properties.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant CMMI-0758651)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant AR60331)en_US
dc.description.sponsorshipUnited States. Dept. of Defense (National Defense Science and Engineering Graduate Fellowship (Grant N00244-09-1-0064))en_US
dc.description.sponsorshipShriners of North Americaen_US
dc.description.sponsorshipDrexel University (Faculty Start-up Grant)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/bm401611ben_US
dc.sourceAmerican Chemical Societyen_US
dc.titleMolecular Adhesion between Cartilage Extracellular Matrix Macromoleculesen_US
dc.typeArticleen_US
dc.identifier.citationRojas, Fredrick P., Michael A. Batista, C. Alexander Lindburg, Delphine Dean, Alan J. Grodzinsky, Christine Ortiz, and Lin Han. “Molecular Adhesion Between Cartilage Extracellular Matrix Macromolecules.” Biomacromolecules 15, no. 3 (March 10, 2014): 772–780. © 2014 American Chemical Society.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.mitauthorRojas, Fredrick P.en_US
dc.contributor.mitauthorBatista, Michael A.en_US
dc.contributor.mitauthorGrodzinsky, Alan J.en_US
dc.contributor.mitauthorOrtiz, Christineen_US
dc.contributor.mitauthorHan, Linen_US
dc.relation.journalBiomacromoleculesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsRojas, Fredrick P.; Batista, Michael A.; Lindburg, C. Alexander; Dean, Delphine; Grodzinsky, Alan J.; Ortiz, Christine; Han, Linen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-3511-5679
dc.identifier.orcidhttps://orcid.org/0000-0002-4942-3456
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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