TY - JOUR
T1 - Ultra-localized single cell electroporation using silicon nanowires
AU - Jokilaakso, Nima
AU - Salm, Eric
AU - Chen, Aaron
AU - Millet, Larry
AU - Guevara, Carlos Duarte
AU - Dorvel, Brian
AU - Reddy, Bobby
AU - Karlstrom, Amelie Eriksson
AU - Chen, Yu
AU - Ji, Hongmiao
AU - Sooryakumar, Ratnasingham
AU - Bashir, Rashid
PY - 2013/2/7
Y1 - 2013/2/7
N2 - Analysis of cell-to-cell variation can further the understanding of intracellular processes and the role of individual cell function within a larger cell population. The ability to precisely lyse single cells can be used to release cellular components to resolve cellular heterogeneity that might be obscured when whole populations are examined. We report a method to position and lyse individual cells on silicon nanowire and nanoribbon biological field effect transistors. In this study, HT-29 cancer cells were positioned on top of transistors by manipulating magnetic beads using external magnetic fields. Ultra-rapid cell lysis was subsequently performed by applying 600-900 mV pp at 10 MHz for as little as 2 ms across the transistor channel and the bulk substrate. We show that the fringing electric field at the device surface disrupts the cell membrane, leading to lysis from irreversible electroporation. This methodology allows rapid and simple single cell lysis and analysis with potential applications in medical diagnostics, proteome analysis and developmental biology studies.
AB - Analysis of cell-to-cell variation can further the understanding of intracellular processes and the role of individual cell function within a larger cell population. The ability to precisely lyse single cells can be used to release cellular components to resolve cellular heterogeneity that might be obscured when whole populations are examined. We report a method to position and lyse individual cells on silicon nanowire and nanoribbon biological field effect transistors. In this study, HT-29 cancer cells were positioned on top of transistors by manipulating magnetic beads using external magnetic fields. Ultra-rapid cell lysis was subsequently performed by applying 600-900 mV pp at 10 MHz for as little as 2 ms across the transistor channel and the bulk substrate. We show that the fringing electric field at the device surface disrupts the cell membrane, leading to lysis from irreversible electroporation. This methodology allows rapid and simple single cell lysis and analysis with potential applications in medical diagnostics, proteome analysis and developmental biology studies.
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U2 - 10.1039/c2lc40837f
DO - 10.1039/c2lc40837f
M3 - Article
C2 - 23179093
AN - SCOPUS:84872085096
SN - 1473-0197
VL - 13
SP - 336
EP - 339
JO - Lab on a Chip - Miniaturisation for Chemistry and Biology
JF - Lab on a Chip - Miniaturisation for Chemistry and Biology
IS - 3
ER -