FluidFM: Combining Atomic Force Microscopy and Nanofluidics in a Universal Liquid Delivery System for Single Cell Applications and Beyond

Nano Letters ◽  
2009 ◽  
Vol 9 (6) ◽  
pp. 2501-2507 ◽  
Author(s):  
André Meister ◽  
Michael Gabi ◽  
Pascal Behr ◽  
Philipp Studer ◽  
János Vörös ◽  
...  
2016 ◽  
Vol 138 (36) ◽  
pp. 11664-11671 ◽  
Author(s):  
Hyunseo Koo ◽  
Ikbum Park ◽  
Yoonhee Lee ◽  
Hyun Jin Kim ◽  
Jung Hoon Jung ◽  
...  

Nanomedicine ◽  
2012 ◽  
Vol 7 (10) ◽  
pp. 1625-1637 ◽  
Author(s):  
Xiaoli Shi ◽  
Xuejie Zhang ◽  
Tie Xia ◽  
Xiaohong Fang

Author(s):  
Christian Enrique García García ◽  
Claude Verdier ◽  
Bernard Lardy ◽  
Frédéric Bossard ◽  
J. Félix Armando Soltero Martínez ◽  
...  

2021 ◽  
Author(s):  
Yuan Qiu ◽  
Chen-Chi Chien ◽  
Basilis Maroulis ◽  
Angelo Gaitas ◽  
Bin Gong

Abstract In this article, a review of the application of atomic force microscopy (AFM) for the analyses of extracellular vesicles is presented. This information is then extended to include fluidic Atomic Force Microscopy (fluidic AFM) applications. Fluidic AFM is an offshoot of AFM that combines a microfluidic cantilever with AFM and has enabled the research community to conduct biological, pathological, and pharmacological studies on cells at the single-cell level in a liquid environment. AFM applications involving single cell and extracellular vesicle studies, colloidal force spectroscopy, and single cell adhesion measurements are discussed. In this review, new results are offered, using fluidic AFM, to illustrate (1) the speed with which sequential measurements of adhesion using coated colloid beads can be done, (2) the ability to assess lateral binding forces (LBFs) of endothelial or epithelial cells in a confluent cell monolayer in appropriate physiological environment, and (3) the ease of measurement of vertical binding force (VBFs) of intercellular adhesion between heterogeneous cells. Finally, key applications are discussed that include extracellular vesicle absorption, manipulation of a single living cell by intracellular injection, sampling of cellular fluid from a single living cell, patch clamping, and mass measurements of a single living cell.


Author(s):  
Kaori Kuribayashi-Shigetomi ◽  
Ryosuke Takahashi ◽  
Agus Subagyo ◽  
Kazuhisa Sueoka ◽  
Takaharu Okajima

2019 ◽  
Author(s):  
Stefania Marcotti ◽  
Gwendolen C Reilly ◽  
Damien Lacroix

AbstractSingle cell mechanical properties represent an increasingly studied descriptor for health and disease. Atomic force microscopy (AFM) has been widely used to measure single cell stiffness, despite its experimental limitations. The development of a computational framework to simulate AFM nanoindentation experiments could be a valuable tool to complement experimental findings. A single cell multi-structural finite element model was designed to this aim by using confocal images of bone cells, comprised of the cell nucleus, cytoplasm and actin cytoskeleton. The computational cell stiffness values were in the range of experimental values acquired on the same cells for nanoindentation of the cell nucleus and periphery, despite showing higher stiffness for the nucleus than for the periphery, oppositely to the average experimental findings. These results suggest it would be of interest to model different single cells with known experimental effective moduli to evaluate the ability of the computational models to replicate experimental results.


2014 ◽  
Vol 6 (14) ◽  
pp. 4932-4955 ◽  
Author(s):  
Kirstin C. Morton ◽  
Lane A. Baker

This review aims to describe the operation of atomic force microscopy related to the study of disease states and single cell analysis, and to serve as an overview of recent advances in this subject area.


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