Water Sorption Induced Transformations in Crystalline Solid Surfaces: Characterization by Atomic Force Microscopy

2010 ◽  
Vol 99 (9) ◽  
pp. 4032-4041 ◽  
Author(s):  
Dabing Chen ◽  
Greg Haugstad ◽  
Zheng Jane Li ◽  
Raj Suryanarayanan
2021 ◽  
Author(s):  
Kohei Kobayashi ◽  
Noriyuki Kodera ◽  
Taishi Kasai ◽  
Yuhei O Tahara ◽  
Takuma Toyonaga ◽  
...  

ABSTRACTMycoplasma mobile, a parasitic bacterium, glides on solid surfaces, such as animal cells and glass by a special mechanism. This process is driven by the force generated through ATP hydrolysis on an internal structure. However, the spatial and temporal behaviors of the internal structures in living cells are unclear. In this study, we detected the movements of the internal structure by scanning cells immobilized on a glass substrate using high-speed atomic force microscopy (HS-AFM). By scanning the surface of a cell, we succeeded in visualizing particles, 2 nm in hight and aligned mostly along the cell axis with a pitch of 31.5 nm, consistent with previously reported features based on electron microscopy. Movements of individual particles were then analyzed by HS-AFM. In the presence of sodium azide, the average speed of particle movements was reduced, suggesting that movement is linked to ATP hydrolysis. Partial inhibition of the reaction by sodium azide enabled us to analyze particle behavior in detail, showing that the particles move 9 nm right, relative to the gliding direction, and 2 nm into the cell interior in 330 ms, then return to their original position, based on ATP hydrolysis.IMPORTANCEThe Mycoplasma genus contains bacteria generally parasitic to animals and plants. Some Mycoplasma species form a protrusion at a pole, bind to solid surfaces, and glide by a special mechanism linked to their infection and survival. The special machinery for gliding can be divided into surface and internal structures that have evolved from rotary motors represented by ATP synthases. This study succeeded in visualizing the real-time movements of the internal structure by scanning from the outside of the cell using an innovative high-speed atomic force microscope, and then analyzing their behaviors.


The Analyst ◽  
2016 ◽  
Vol 141 (3) ◽  
pp. 1017-1026 ◽  
Author(s):  
I. Sokolov ◽  
G. Zorn ◽  
J. M. Nichols

The study of molecular adsorption on solid surfaces is of broad interest.


2007 ◽  
Vol 5 (2-3) ◽  
pp. 49-60 ◽  
Author(s):  
Hans-Juergen Butt ◽  
Jijun Wang ◽  
Rüdiger Stark ◽  
Michael Kappl ◽  
Bernhard Anton Wolf ◽  
...  

2014 ◽  
Vol 2 (3) ◽  
pp. 151-159 ◽  
Author(s):  
Marta Krasowska ◽  
Anna Niecikowska ◽  
David A. Beattie

1998 ◽  
Vol 66 (7) ◽  
pp. S349-S352 ◽  
Author(s):  
T. Miyatani ◽  
S. Okamoto ◽  
A. Rosa ◽  
O. Marti ◽  
M. Fujihira

Polymer ◽  
2006 ◽  
Vol 47 (20) ◽  
pp. 7259-7270 ◽  
Author(s):  
Rüdiger Stark ◽  
Elmar Bonaccurso ◽  
Michael Kappl ◽  
Hans-Jürgen Butt

mBio ◽  
2021 ◽  
Vol 12 (3) ◽  
Author(s):  
Kohei Kobayashi ◽  
Noriyuki Kodera ◽  
Taishi Kasai ◽  
Yuhei O. Tahara ◽  
Takuma Toyonaga ◽  
...  

ABSTRACT Mycoplasma mobile, a parasitic bacterium, glides on solid surfaces, such as animal cells and glass, by a special mechanism. This process is driven by the force generated through ATP hydrolysis on an internal structure. However, the spatial and temporal behaviors of the internal structures in living cells are unclear. In this study, we detected the movements of the internal structure by scanning cells immobilized on a glass substrate using high-speed atomic force microscopy (HS-AFM). By scanning the surface of a cell, we succeeded in visualizing particles, 2 nm in height and aligned mostly along the cell axis with a pitch of 31.5 nm, consistent with previously reported features based on electron microscopy. Movements of individual particles were then analyzed by HS-AFM. In the presence of sodium azide, the average speed of particle movements was reduced, suggesting that movement is linked to ATP hydrolysis. Partial inhibition of the reaction by sodium azide enabled us to analyze particle behavior in detail, showing that the particles move 9 nm right, relative to the gliding direction, and 2 nm into the cell interior in 330 ms and then return to their original position, based on ATP hydrolysis. IMPORTANCE The Mycoplasma genus contains bacteria generally parasitic to animals and plants. Some Mycoplasma species form a protrusion at a pole, bind to solid surfaces, and glide by a special mechanism linked to their infection and survival. The special machinery for gliding can be divided into surface and internal structures that have evolved from rotary motors represented by ATP synthases. This study succeeded in visualizing the real-time movements of the internal structure by scanning from the outside of the cell using an innovative high-speed atomic force microscope and then analyzing their behaviors.


2006 ◽  
Vol 59 (6) ◽  
pp. 394
Author(s):  
Teiji Kato ◽  
Takayuki Nakakawaji

Cryogenic Atomic Force Microscopy (AFM) was used to observe perfluoropolyether (PFPE) lubricant molecules at atomically flat solid surfaces and at a magnetic disk surface to understand the lubricity of ultra-thin (1 nm) lubricant layers at the hard disk surface. Molecular imaging of PFPE lubricant molecules reveals the formation of reversed micelle structures at comparatively non-polar solid surfaces such as gold or the carbon overcoat of magnetic disks.


2008 ◽  
Vol 14 (2) ◽  
pp. 150-158 ◽  
Author(s):  
Ricardo P. Santos ◽  
Theodora T.P. Arruda ◽  
Cibele B.M. Carvalho ◽  
Victor A. Carneiro ◽  
Lara Q.V. Braga ◽  
...  

Biofilms are assemblages of microorganisms and their associated extracellular products at an interface and typically with an abiotic or biotic surface. The study of the morphology of biofilms is important because they are associated with processes of biofouling, corrosion, catalysis, pollutant transformation, dental caries, drug resistance, and so forth. In the literature, biofilms have been examined by atomic force microscopy (AFM), which has proven to be a potent tool to study different aspects of the biofilm development on solid surfaces. In this work, we used AFM to investigate topographical changes during the development process ofEnterococcus faecalisbiofilms, which were generated on sterile cellulose nitrate membrane (CNM) filters in brain heart infusion (BHI) broth agar blood plates after 24, 36, 72, 192, and 360 h. AFM height images showed topographical changes due to biofilm development, which were used to characterize several aspects of the bacterial surface, such as the presence of extracellular polymeric substance, and the biofilm development stage. Changes in the development stage of the biofilm were shown to correlate with changes in the surface roughness as quantified through the mean roughness.


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