Fundamentals and Applications of FluidFM Technology in Single-Cell Studies

被引:23
作者
Saha, Prithwidip [1 ,2 ]
Duanis-Assaf, Tal [1 ,2 ]
Reches, Meital [1 ,2 ]
机构
[1] Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Ctr Nanosci & Nanotechnol, IL-91904 Jerusalem, Israel
关键词
atomic force microscopy; biomaterials; cell adhesion; fluidFM technology; fluidic force microscopy; intracellular injection; extraction; single-cell force spectroscopy; ATOMIC-FORCE MICROSCOPY; INTERCELLULAR-ADHESION FORCES; MICROMACHINED FOUNTAIN PEN; BACTERIAL ADHESION; MECHANICAL-PROPERTIES; NANOFOUNTAIN-PROBE; ELASTIC PROPERTIES; LIVING CELLS; SURFACES; AFM;
D O I
10.1002/admi.202001115
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This review describes the potential of FluidFM technology and its implementation in studying the interface between a single cell (prokaryote or eukaryote) and a surface or a surrounding area. A combination of microfluidics with conventional atomic force microscope (AFM) makes this platform efficient to address challenges associated with various biomolecular systems and biophysical activities down to single-cell levels. Upon regulating the pressure through a microchanneled cantilever via a pressure controller, a wide range of studies are feasible. These include isolating and displacing a single living cell to measure the cell-substrate and intercellular adhesion forces, intracellular injection of biomolecules as drug delivery systems, extraction of cellular fluid for downstream analyses, and characterization of cell structures to obtain the mechanical properties. For single-cell adhesion experiments, the irreversible chemical-based cell immobolization in conventional AFM has been replaced with the reversible pressure-controlled approach in this platform; this not only reduces the experiment time-it also helps in performing serial and rapid measurement with improved statistics. This approach also ensures the retention of cell viability after each experiment.
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页数:14
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