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dc.contributor.authorPeng, Zhangli
dc.contributor.authorDao, Ming
dc.contributor.authorSuresh, Subra
dc.contributor.authorLi, Xuejin
dc.contributor.authorPivkin, Igor V.
dc.contributor.authorKarniadakis, George E.
dc.date.accessioned2014-03-24T19:26:27Z
dc.date.available2014-03-24T19:26:27Z
dc.date.issued2013-08
dc.date.submitted2013-05
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/85915
dc.description.abstractWe study the biomechanical interactions between the lipid bilayer and the cytoskeleton in a red blood cell (RBC) by developing a general framework for mesoscopic simulations. We treated the lipid bilayer and the cytoskeleton as two distinct components and developed a unique whole-cell model of the RBC, using dissipative particle dynamics (DPD). The model is validated by comparing the predicted results with measurements from four different and independent experiments. First, we simulated the micropipette aspiration and quantified the cytoskeletal deformation. Second, we studied the membrane fluctuations of healthy RBCs and RBCs parasitized to different intraerythrocytic stages by the malaria-inducing parasite Plasmodium falciparum. Third, we subjected the RBC to shear flow and investigated the dependence of its tank-treading frequency on shear rate. Finally, we simulated the bilayer–cytoskeletal detachment in channel flow to quantify the strength of such interactions when the corresponding bonds break. Taken together, these experiments and corresponding systematic DPD simulations probe the governing constitutive response of the cytoskeleton, elastic stiffness, viscous friction, and strength of bilayer–cytoskeletal interactions as well as membrane viscosities. Hence, the DPD simulations and comparisons with available independent experiments serve as validation of the unique two-component model and lead to useful insights into the biomechanical interactions between the lipid bilayer and the cytoskeleton of the RBC. Furthermore, they provide a basis for further studies to probe cell mechanistic processes in health and disease in a manner that guides the design and interpretation of experiments and to develop simulations of phenomena that cannot be studied systematically by experiments alone.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01HL094270)en_US
dc.description.sponsorshipUnited States. Dept. of Energy (Collaboratory on Mathematics and Mesoscopic Modeling of Materials)en_US
dc.description.sponsorshipSingapore-MIT Alliance for Research and Technology Centeren_US
dc.description.sponsorshipSingapore-MIT Allianceen_US
dc.language.isoen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1311827110en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceNational Academy of Science (U.S.)en_US
dc.titleLipid bilayer and cytoskeletal interactions in a red blood cellen_US
dc.typeArticleen_US
dc.identifier.citationPeng, Z., X. Li, I. V. Pivkin, M. Dao, G. E. Karniadakis, and S. Suresh. “Lipid Bilayer and Cytoskeletal Interactions in a Red Blood Cell.” Proceedings of the National Academy of Sciences 110, no. 33 (August 13, 2013): 13356–13361.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.mitauthorPeng, Zhanglien_US
dc.contributor.mitauthorDao, Mingen_US
dc.contributor.mitauthorSuresh, Subraen_US
dc.relation.journalProceedings of the National Academy of Sciencesen_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.orderedauthorsPeng, Z.; Li, X.; Pivkin, I. V.; Dao, M.; Karniadakis, G. E.; Suresh, S.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6223-6831
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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