Live cell near-field optical imaging and voltage sensing with ultrasensitive force control

被引:1
作者
Brahami, Aaron [1 ]
Levy, Hadas [1 ]
Zlotkin-Rivkin, Efrat [2 ]
Melamed-Book, Naomi [3 ]
Tal, Nataly [1 ]
Lev, Dmitry [1 ]
Yeshua, Talia [1 ]
Fedosyeyev, Oleg [4 ]
Aroeti, Benjamin [2 ]
Lewis, Aaron [1 ]
机构
[1] Rachel & Selim Benin Sch Comp Sci & Engn, Dept Appl Phys, Ctr NanoSci & NanoTechnol, Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Alexander Silberman Inst Life Sci, Dept Cell & Dev Biol, Fac Sci, Jerusalem, Israel
[3] Alexander Silberman Inst Life Sci, Confocal Unit, Jerusalem, Israel
[4] Nanon Imaging Ltd, Jerusalem, Israel
基金
以色列科学基金会;
关键词
FLUORESCENCE CORRELATION SPECTROSCOPY; MICROSCOPY; LIQUID; MEMBRANES; MICROVILLI; PROBES;
D O I
10.1364/OE.25.012131
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
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 (similar to 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. (C) 2017 Optical Society of America
引用
收藏
页码:12131 / 12143
页数:13
相关论文
共 26 条
[1]   Intracellular and extracellular forces drive primary cilia movement [J].
Battle, Christopher ;
Ott, Carolyn M. ;
Burnette, Dylan T. ;
Lippincott-Schwartz, Jennifer ;
Schmidt, Christoph F. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (05) :1410-1415
[2]   Tissue-engineered kidney disease models [J].
DesRochers, Teresa M. ;
Palma, Erica ;
Kaplan, David L. .
ADVANCED DRUG DELIVERY REVIEWS, 2014, 69 :67-80
[3]   Advances in atomic force microscopy [J].
Giessibl, FJ .
REVIEWS OF MODERN PHYSICS, 2003, 75 (03) :949-983
[4]   Fundamental limits to force detection using quartz tuning forks [J].
Grober, RD ;
Acimovic, J ;
Schuck, J ;
Hessman, D ;
Kindlemann, PJ ;
Hespanha, J ;
Morse, AS ;
Karrai, K ;
Tiemann, I ;
Manus, S .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2000, 71 (07) :2776-2780
[5]   Scanning near-field optical microscopy of a cell membrane in liquid [J].
Höppener, C ;
Molenda, D ;
Fuchs, H ;
Naber, A .
JOURNAL OF MICROSCOPY-OXFORD, 2003, 210 :288-293
[6]  
Ianoul A, 2004, BIOPHYS J, V87, P3525, DOI 10.1529/biophysj.104.046393
[7]   PIEZOELECTRIC TIP-SAMPLE DISTANCE CONTROL FOR NEAR-FIELD OPTICAL MICROSCOPES [J].
KARRAI, K ;
GROBER, RD .
APPLIED PHYSICS LETTERS, 1995, 66 (14) :1842-1844
[8]   Mapping the mechanical action of light [J].
Kohlgraf-Owens, Dana C. ;
Sukhov, Sergey ;
Dogariu, Aristide .
PHYSICAL REVIEW A, 2011, 84 (01)
[9]   Near-field scanning optical microscopy in liquid for high resolution single molecule detection on dendritic cells [J].
Koopman, M ;
Cambi, A ;
de Bakker, BI ;
Joosten, B ;
Figdor, CG ;
van Hulst, NF ;
Garcia-Parajo, MF .
FEBS LETTERS, 2004, 573 (1-3) :6-10
[10]   Topography and near-field image measurement of soft biological samples in liquid by using a tuning fork based bent optical-fiber sensor [J].
Kwon, Sangjin ;
Jeong, Sungho ;
Kang, Yongseok .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2011, 82 (04)