Development of a platform for single cell genomics using convex lens-induced confinement
We demonstrate a lab-on-a-chip that combines micro/nano-fabricated features with a Convex Lens-Induced Confinement (CLIC) device for the in situ analysis of single cells. A complete cycle of single cell analysis was achieved that includes: cell trapping, cell isolation, lysis, protein digestion, gen...
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Veröffentlicht in: | Lab on a chip 2015-07, Vol.15 (14), p.313-32 |
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creator | Mahshid, Sara Ahamed, Mohammed Jalal Berard, Daniel Amin, Susan Sladek, Robert Leslie, Sabrina R Reisner, Walter |
description | We demonstrate a lab-on-a-chip that combines micro/nano-fabricated features with a Convex Lens-Induced Confinement (CLIC) device for the
in situ
analysis of single cells. A complete cycle of single cell analysis was achieved that includes: cell trapping, cell isolation, lysis, protein digestion, genomic DNA extraction and on-chip genomic DNA linearization. The ability to dynamically alter the flow-cell dimensions using the CLIC method was coupled with a flow-control mechanism for achieving efficient cell trapping, buffer exchange, and loading of long DNA molecules into nanofluidic arrays. Finite element simulation of fluid flow gives rise to optimized design parameters for overcoming the high hydraulic resistance present in the micro/nano-confinement region. By tuning design parameters such as the pressure gradient and CLIC confinement, an efficient on-chip single cell analysis protocol can be obtained. We demonstrate that we can extract Mbp long genomic DNA molecules from a single human lybphoblastoid cell and stretch these molecules in the nanochannels for optical interrogation.
We present a lab-on-a-chip for the next generation of single-cell genomics, performing full-cycle single-cell analysis by demonstrating mega-base pair genomic DNAs in nanochannels extracted
in situ
. |
doi_str_mv | 10.1039/c5lc00492f |
format | Article |
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in situ
analysis of single cells. A complete cycle of single cell analysis was achieved that includes: cell trapping, cell isolation, lysis, protein digestion, genomic DNA extraction and on-chip genomic DNA linearization. The ability to dynamically alter the flow-cell dimensions using the CLIC method was coupled with a flow-control mechanism for achieving efficient cell trapping, buffer exchange, and loading of long DNA molecules into nanofluidic arrays. Finite element simulation of fluid flow gives rise to optimized design parameters for overcoming the high hydraulic resistance present in the micro/nano-confinement region. By tuning design parameters such as the pressure gradient and CLIC confinement, an efficient on-chip single cell analysis protocol can be obtained. We demonstrate that we can extract Mbp long genomic DNA molecules from a single human lybphoblastoid cell and stretch these molecules in the nanochannels for optical interrogation.
We present a lab-on-a-chip for the next generation of single-cell genomics, performing full-cycle single-cell analysis by demonstrating mega-base pair genomic DNAs in nanochannels extracted
in situ
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in situ
analysis of single cells. A complete cycle of single cell analysis was achieved that includes: cell trapping, cell isolation, lysis, protein digestion, genomic DNA extraction and on-chip genomic DNA linearization. The ability to dynamically alter the flow-cell dimensions using the CLIC method was coupled with a flow-control mechanism for achieving efficient cell trapping, buffer exchange, and loading of long DNA molecules into nanofluidic arrays. Finite element simulation of fluid flow gives rise to optimized design parameters for overcoming the high hydraulic resistance present in the micro/nano-confinement region. By tuning design parameters such as the pressure gradient and CLIC confinement, an efficient on-chip single cell analysis protocol can be obtained. We demonstrate that we can extract Mbp long genomic DNA molecules from a single human lybphoblastoid cell and stretch these molecules in the nanochannels for optical interrogation.
We present a lab-on-a-chip for the next generation of single-cell genomics, performing full-cycle single-cell analysis by demonstrating mega-base pair genomic DNAs in nanochannels extracted
in situ
.</description><subject>Arrays</subject><subject>Cells, Cultured</subject><subject>Computational fluid dynamics</subject><subject>Confinement</subject><subject>Deoxyribonucleic acid</subject><subject>Design parameters</subject><subject>DNA - genetics</subject><subject>Fluid flow</subject><subject>Genomics</subject><subject>Humans</subject><subject>Lenses</subject><subject>Microfluidic Analytical Techniques - instrumentation</subject><subject>Nanostructure</subject><subject>Nanotechnology - instrumentation</subject><subject>Single-Cell Analysis - instrumentation</subject><subject>Trapping</subject><issn>1473-0197</issn><issn>1473-0189</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1LxDAUxIMorq5evCvxJkI1H03aHqW6Kix4UfBW0uRlqaRpbbaL_ve27rre9JKEmR_DexOETii5ooRn11o4TUicMbuDDmic8IjQNNvdvrNkgg5DeCOEilim-2jCJJGMUHqAXm9hBa5pa_BL3FiscOvU0jZdjYcDh8ovHGANzuEF-KaudMD9qGLd-BV8YAc-RJU3vQYzarbyMIYdoT2rXIDjzT1FL7O75_whmj_dP-Y380hzmS4jndnEsNKAlkaZYQVpjAIRi1IT4MASKkymSsuZTZigWujESq1AyVQCiSWfoot1bts17z2EZVFXYZxXeWj6UNBEcMEJYfR_VGZsoBMaD-jlGtVdE0IHtmi7qlbdZ0FJMZZe5GKef5c-G-CzTW5f1mC26E_LA3C6Brqgt-7vrw3--V9-0RrLvwDbbZMn</recordid><startdate>20150721</startdate><enddate>20150721</enddate><creator>Mahshid, Sara</creator><creator>Ahamed, Mohammed Jalal</creator><creator>Berard, Daniel</creator><creator>Amin, Susan</creator><creator>Sladek, Robert</creator><creator>Leslie, Sabrina R</creator><creator>Reisner, Walter</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7SP</scope><scope>7TB</scope><scope>7U5</scope><scope>8FD</scope><scope>FR3</scope><scope>L7M</scope></search><sort><creationdate>20150721</creationdate><title>Development of a platform for single cell genomics using convex lens-induced confinement</title><author>Mahshid, Sara ; Ahamed, Mohammed Jalal ; Berard, Daniel ; Amin, Susan ; Sladek, Robert ; Leslie, Sabrina R ; Reisner, Walter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-c9f7d2bdec6dad92f6ddae545bc0e3e2715d9abf32f7251c5c7f6caea686e0463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Arrays</topic><topic>Cells, Cultured</topic><topic>Computational fluid dynamics</topic><topic>Confinement</topic><topic>Deoxyribonucleic acid</topic><topic>Design parameters</topic><topic>DNA - genetics</topic><topic>Fluid flow</topic><topic>Genomics</topic><topic>Humans</topic><topic>Lenses</topic><topic>Microfluidic Analytical Techniques - instrumentation</topic><topic>Nanostructure</topic><topic>Nanotechnology - instrumentation</topic><topic>Single-Cell Analysis - instrumentation</topic><topic>Trapping</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mahshid, Sara</creatorcontrib><creatorcontrib>Ahamed, Mohammed Jalal</creatorcontrib><creatorcontrib>Berard, Daniel</creatorcontrib><creatorcontrib>Amin, Susan</creatorcontrib><creatorcontrib>Sladek, Robert</creatorcontrib><creatorcontrib>Leslie, Sabrina R</creatorcontrib><creatorcontrib>Reisner, Walter</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Electronics & Communications Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Lab on a chip</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mahshid, Sara</au><au>Ahamed, Mohammed Jalal</au><au>Berard, Daniel</au><au>Amin, Susan</au><au>Sladek, Robert</au><au>Leslie, Sabrina R</au><au>Reisner, Walter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a platform for single cell genomics using convex lens-induced confinement</atitle><jtitle>Lab on a chip</jtitle><addtitle>Lab Chip</addtitle><date>2015-07-21</date><risdate>2015</risdate><volume>15</volume><issue>14</issue><spage>313</spage><epage>32</epage><pages>313-32</pages><issn>1473-0197</issn><eissn>1473-0189</eissn><abstract>We demonstrate a lab-on-a-chip that combines micro/nano-fabricated features with a Convex Lens-Induced Confinement (CLIC) device for the
in situ
analysis of single cells. A complete cycle of single cell analysis was achieved that includes: cell trapping, cell isolation, lysis, protein digestion, genomic DNA extraction and on-chip genomic DNA linearization. The ability to dynamically alter the flow-cell dimensions using the CLIC method was coupled with a flow-control mechanism for achieving efficient cell trapping, buffer exchange, and loading of long DNA molecules into nanofluidic arrays. Finite element simulation of fluid flow gives rise to optimized design parameters for overcoming the high hydraulic resistance present in the micro/nano-confinement region. By tuning design parameters such as the pressure gradient and CLIC confinement, an efficient on-chip single cell analysis protocol can be obtained. We demonstrate that we can extract Mbp long genomic DNA molecules from a single human lybphoblastoid cell and stretch these molecules in the nanochannels for optical interrogation.
We present a lab-on-a-chip for the next generation of single-cell genomics, performing full-cycle single-cell analysis by demonstrating mega-base pair genomic DNAs in nanochannels extracted
in situ
.</abstract><cop>England</cop><pmid>26062011</pmid><doi>10.1039/c5lc00492f</doi><tpages>8</tpages></addata></record> |
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language | eng |
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source | MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Arrays Cells, Cultured Computational fluid dynamics Confinement Deoxyribonucleic acid Design parameters DNA - genetics Fluid flow Genomics Humans Lenses Microfluidic Analytical Techniques - instrumentation Nanostructure Nanotechnology - instrumentation Single-Cell Analysis - instrumentation Trapping |
title | Development of a platform for single cell genomics using convex lens-induced confinement |
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