TY - JOUR
T1 - Live cell near-field optical imaging and voltage sensing with ultrasensitive force control
AU - Brahami, Aaron
AU - Levy, Hadas
AU - Zlotkin-Rivkin, Efrat
AU - Melamed-Book, Naomi
AU - Tal, Nataly
AU - Lev, Dmitry
AU - Yeshua, Talia
AU - Fedosyeyev, Oleg
AU - Aroeti, Benjamin
AU - Lewis, Aaron
N1 - Publisher Copyright:
© 2017 Optical Society of America.
PY - 2017/5/29
Y1 - 2017/5/29
N2 - Force controlled optical imaging of membranes of living cells is demonstrated. Such imaging has been extended to image membrane potential changes to demonstrate that live cell imaging has been achieved. To accomplish this advance, limitations inherent in atomic force microscopy (AFM) since its inception in 1986 [G. Binnig, C. F. Quate, and C. Gerber, "Atomic Force Microscope," Phys. Rev. Lett. 56, 930-933 (1986).] had to be overcome. The advances allow for live cell imaging of a whole genre of functional biological imaging with stiff (1-10N/m) scanned probe imaging cantilevers. Even topographic imaging of fine cell protrusions, such as microvilli, has been accomplished with such cantilevers. Similar topographic imaging has only recently been demonstrated with the standard soft (0.05N/m) cantilevers that are generally required for live cell imaging. The progress reported here demonstrates both ultrasensitive AFM (∼100pN), capable of topographic imaging of even microvilli protruding from cell membranes and new functional applications that should have a significant impact on optical and other approaches in biological imaging of living systems and ultrasoft materials.
AB - Force controlled optical imaging of membranes of living cells is demonstrated. Such imaging has been extended to image membrane potential changes to demonstrate that live cell imaging has been achieved. To accomplish this advance, limitations inherent in atomic force microscopy (AFM) since its inception in 1986 [G. Binnig, C. F. Quate, and C. Gerber, "Atomic Force Microscope," Phys. Rev. Lett. 56, 930-933 (1986).] had to be overcome. The advances allow for live cell imaging of a whole genre of functional biological imaging with stiff (1-10N/m) scanned probe imaging cantilevers. Even topographic imaging of fine cell protrusions, such as microvilli, has been accomplished with such cantilevers. Similar topographic imaging has only recently been demonstrated with the standard soft (0.05N/m) cantilevers that are generally required for live cell imaging. The progress reported here demonstrates both ultrasensitive AFM (∼100pN), capable of topographic imaging of even microvilli protruding from cell membranes and new functional applications that should have a significant impact on optical and other approaches in biological imaging of living systems and ultrasoft materials.
UR - http://www.scopus.com/inward/record.url?scp=85019969490&partnerID=8YFLogxK
U2 - 10.1364/OE.25.012131
DO - 10.1364/OE.25.012131
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C2 - 28786571
AN - SCOPUS:85019969490
SN - 1094-4087
VL - 25
SP - 12131
EP - 12143
JO - Optics Express
JF - Optics Express
IS - 11
ER -