TY - JOUR
T1 - Transfected single-cell imaging by scanning electrochemical optical microscopy with shear force feedback regulation
AU - Takahashi, Yasufumi
AU - Shiku, Hitoshi
AU - Murata, Tatsuya
AU - Yasukawa, Tomoyuki
AU - Matsue, Tomokazu
PY - 2009/12/1
Y1 - 2009/12/1
N2 - Gene-transfected single HeLa cells were characterized using a scanning electrochemical/optical microscope (SECM/OM) system with shear-force-based probe-sample distance regulation to simultaneously capture electrochemical, fluorescent, and topographic images. The outer and inner states of single living cells were obtained as electrochemical and fluorescent signals, respectively, by using an optical fiber-nanoelectrode probe. A focused ion beam (FIB) was used to mill the optical aperture and the ring electrode at the probe apex (the inner and outer radii of the ring electrode were 37 and 112 nm, respectively). To apply an appropriate shear force between the probe tip and the living cell surface, we optimized the amplitude of oscillation of the tuning fork to which the probe was attached. Field-programmable gate arrays (FPGA) were adopted to drastically increase the feedback speed of the tip-sample distance regulation, shorten the scanning time for imaging, and enhance the accuracy and quality of the living cell images. In employing these improvements, we simultaneously measured the cellular expression activity of both secreted alkaline phosphatase outside and GFP inside by using the SECM/OM with shear force distance regulation.
AB - Gene-transfected single HeLa cells were characterized using a scanning electrochemical/optical microscope (SECM/OM) system with shear-force-based probe-sample distance regulation to simultaneously capture electrochemical, fluorescent, and topographic images. The outer and inner states of single living cells were obtained as electrochemical and fluorescent signals, respectively, by using an optical fiber-nanoelectrode probe. A focused ion beam (FIB) was used to mill the optical aperture and the ring electrode at the probe apex (the inner and outer radii of the ring electrode were 37 and 112 nm, respectively). To apply an appropriate shear force between the probe tip and the living cell surface, we optimized the amplitude of oscillation of the tuning fork to which the probe was attached. Field-programmable gate arrays (FPGA) were adopted to drastically increase the feedback speed of the tip-sample distance regulation, shorten the scanning time for imaging, and enhance the accuracy and quality of the living cell images. In employing these improvements, we simultaneously measured the cellular expression activity of both secreted alkaline phosphatase outside and GFP inside by using the SECM/OM with shear force distance regulation.
UR - http://www.scopus.com/inward/record.url?scp=73249128476&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=73249128476&partnerID=8YFLogxK
U2 - 10.1021/ac901796r
DO - 10.1021/ac901796r
M3 - Article
C2 - 19883061
AN - SCOPUS:73249128476
SN - 0003-2700
VL - 81
SP - 9674
EP - 9681
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 23
ER -