scholarly journals Capsular polysaccharide production from Zunongwangia profunda SM-A87 monitored at single cell level by atomic force microscopy

Author(s):  
Kang Li ◽  
Long-Sheng Zhao ◽  
He-Min Sun ◽  
Ruo-Cong Tang ◽  
Zhi-Hua Chen ◽  
...  
2011 ◽  
Vol 100 (3) ◽  
pp. 564-572 ◽  
Author(s):  
Takahiro Watanabe-Nakayama ◽  
Shin-ichi Machida ◽  
Ichiro Harada ◽  
Hiroshi Sekiguchi ◽  
Rehana Afrin ◽  
...  

2019 ◽  
Author(s):  
Mengdan Chen ◽  
Jinshu Zeng ◽  
Weiwei Ruan ◽  
Zhenghong Zhang ◽  
Yuhua Wang ◽  
...  

Cellular mechanical properties could serve as a prominent indicator for disease progression and early cancer diagnosis. This study utilized atomic force microscopy (AFM) to measure the viscoelastic properties and then examined their association with the invasion of ovarian cancer at living single cell level. The results demonstrated the elasticity and viscosity of ovarian cancer cell OVCAR-3 and HO-8910 significantly decreased than those of HOSEpiC, the ovarian cancer control cell. Further examination found the dramatic increase of migration/invasion and the obvious decease of microfilament density in OVCAR-3 and HO-8910 cells compared with those of HOSEpiC cells. And there was a significant relationship between viscoelastic and biological properties among these cells. In addition, the elasticity was significantly increased in OVCAR-3 and HO-8910 cells after the treatment of anticancer compound echinomycin (Ech), while no obvious change was found in HOSEpiC cells after Ech treatment. Interestingly, Ech seemed no effects on the viscosity of these cells. Furthermore, Ech significantly inhibited the migration/invasion and significantly increased the microfilament density in OVCAR-3 and HO-8910 cells compared with those of HOSEpiC cells, which was significantly related with the elasticity among these cells. Notably, an increase of elasticity and a decrease of invasion were found in OVCAR-3 and HO-8910 cells with Ech treatment. Together, this study clearly demonstrated the association of viscoelastic properties with the invasion of ovarian cancer cells and shed a light on the biomechanical changes for early diagnosis of tumor transformation and progression at single cell level.


Nano Research ◽  
2021 ◽  
Author(s):  
Mi Li ◽  
Lianqing Liu ◽  
Tomaso Zambelli

AbstractFluidic force microscopy (FluidFM), which combines atomic force microscopy (AFM) with microchanneled cantilevers connected to a pressure controller, is a technique allowing the realization of force-sensitive nanopipette under aqueous conditions. FluidFM has unique advantages in simultaneous three-dimensional manipulations and mechanical measurements of biological specimens at the micro-/nanoscale. Over the past decade, FluidFM has shown its potential in biophysical assays particularly in the investigations at single-cell level, offering novel possibilities for discovering the underlying mechanisms guiding life activities. Here, we review the utilization of FluidFM to address biomechanical and biophysical issues in the life sciences. Firstly, the fundamentals of FluidFM are represented. Subsequently, the applications of FluidFM for biophysics at single-cell level are surveyed from several facets, including single-cell manipulations, single-cell force spectroscopy, and single-cell electrophysiology. Finally, the challenges and perspectives for future progressions are provided.


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

Nano Letters ◽  
2009 ◽  
Vol 9 (6) ◽  
pp. 2501-2507 ◽  
Author(s):  
André Meister ◽  
Michael Gabi ◽  
Pascal Behr ◽  
Philipp Studer ◽  
János Vörös ◽  
...  

2015 ◽  
Vol 12 (103) ◽  
pp. 20141109 ◽  
Author(s):  
Congzhou Wang ◽  
Christopher J. Ehrhardt ◽  
Vamsi K. Yadavalli

Cell surface carbohydrates are important to various bacterial activities and functions. It is well known that different types of Bacillus display heterogeneity of surface carbohydrate compositions, but detection of their presence, quantitation and estimation of variation at the single cell level have not been previously solved. Here, using atomic force microscopy (AFM)-based recognition force mapping coupled with lectin probes, the specific carbohydrate distributions of N -acetylglucosamine and mannose/glucose were detected, mapped and quantified on single B. cereus surfaces at the nanoscale across the entire cell. Further, the changes of the surface carbohydrate compositions from the vegetative cell to spore were shown. These results demonstrate AFM-based ‘recognition force mapping’ as a versatile platform to quantitatively detect and spatially map key bacterial surface biomarkers (such as carbohydrate compositions), and monitor in situ changes in surface biochemical properties during intracellular activities at the single cell level.


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.


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