Show simple item record

dc.contributor.authorCermak, Nathan
dc.contributor.authorA Murakami, Mark
dc.contributor.authorOgawa, Masaaki
dc.contributor.authorAgache, Vincent
dc.contributor.authorBaléras, François
dc.contributor.authorWeinstock, David M
dc.contributor.authorOlcum, Selim A.
dc.contributor.authorDelgado, Francisco Feijo
dc.contributor.authorWasserman, Steven
dc.contributor.authorKnudsen, Scott
dc.contributor.authorKimmerling, Robert John
dc.contributor.authorStevens, Mark M.
dc.contributor.authorKikuchi, Yuki
dc.contributor.authorSandikci, Arzu
dc.contributor.authorManalis, Scott R
dc.contributor.authorPayer, Kristofor Robert
dc.date.accessioned2018-09-10T19:54:39Z
dc.date.available2018-09-10T19:54:39Z
dc.date.issued2016-09
dc.date.submitted2015-11
dc.identifier.issn1087-0156
dc.identifier.issn1546-1696
dc.identifier.urihttp://hdl.handle.net/1721.1/117696
dc.description.abstractMethods to rapidly assess cell growth would be useful for many applications, including drug susceptibility testing, but current technologies have limited sensitivity or throughput. Here we present an approach to precisely and rapidly measure growth rates of many individual cells simultaneously. We flow cells in suspension through a microfluidic channel with 10-12 resonant mass sensors distributed along its length, weighing each cell repeatedly over the 4-20 min it spends in the channel. Because multiple cells traverse the channel at the same time, we obtain growth rates for >60 cells/h with a resolution of 0.2 pg/h for mammalian cells and 0.02 pg/h for bacteria. We measure the growth of single lymphocytic cells, mouse and human T cells, primary human leukemia cells, yeast, Escherichia coli and Enterococcus faecalis. Our system reveals subpopulations of cells with divergent growth kinetics and enables assessment of cellular responses to antibiotics and antimicrobial peptides within minutes.en_US
dc.description.sponsorshipUnited States. Army Research Office (Grant W911NF-09-D-0001)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant 1129359)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Grant U54CA143874)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Grant P30-CA14051)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Grant R33-CA191143)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant T32-GM008334)en_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (Grant T32-GM008334)en_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/NBT.3666en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleHigh-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arraysen_US
dc.typeArticleen_US
dc.identifier.citationCermak, Nathan et al. “High-Throughput Measurement of Single-Cell Growth Rates Using Serial Microfluidic Mass Sensor Arrays.” Nature Biotechnology 34, 10 (September 2016): 1052–1059en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Microsystems Technology Laboratoriesen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorOlcum, Selim A.
dc.contributor.mitauthorDelgado, Francisco Feijo
dc.contributor.mitauthorWasserman, Steven
dc.contributor.mitauthorPayer, Kristofor
dc.contributor.mitauthorKnudsen, Scott
dc.contributor.mitauthorKimmerling, Robert John
dc.contributor.mitauthorStevens, Mark M.
dc.contributor.mitauthorKikuchi, Yuki
dc.contributor.mitauthorSandikci, Arzu
dc.contributor.mitauthorManalis, Scott R
dc.relation.journalNature Biotechnologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-09-10T15:43:58Z
dspace.orderedauthorsCermak, Nathan; Olcum, Selim; Delgado, Francisco Feijó; Wasserman, Steven C; Payer, Kristofor R; A Murakami, Mark; Knudsen, Scott M; Kimmerling, Robert J; Stevens, Mark M; Kikuchi, Yuki; Sandikci, Arzu; Ogawa, Masaaki; Agache, Vincent; Baléras, François; Weinstock, David M; Manalis, Scott Ren_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6417-1007
dc.identifier.orcidhttps://orcid.org/0000-0002-5866-4606
dc.identifier.orcidhttps://orcid.org/0000-0001-9939-764X
dc.identifier.orcidhttps://orcid.org/0000-0002-5702-8667
dc.identifier.orcidhttps://orcid.org/0000-0002-7773-194X
dc.identifier.orcidhttps://orcid.org/0000-0001-5223-9433
mit.licenseOPEN_ACCESS_POLICYen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record