Characterization of organic monolayers on individual microparticles using microprobe mass spectrometry

Author(s):  
Thomas Fister ◽  
John Chakel ◽  
Robert Odom ◽  
Filippo Radicati di Brozolo ◽  
Richard W. Linton

Polycyclic organic matter (POM) represents a class of compounds of environmental significance. Many of these compounds have been shown to exhibit mutagenic characteristics. POM is formed during the combustion of fossil fuels such as coal. Emitted particulate matter such as coal flyash contains surface associated POM that undergoes chemical transformations due to photolysis and exposure to gaseous pollutants. Past studies of these compounds on flyash have relied on wet chemical techniques in which POM is extracted from large quantities of flyash and then analyzed by chromatography. This technique is hindered by several problems such as the extensive heterogeneity in flyash composition. Individual flyash particles of different composition will influence POM adsorption and reactivity. Studies of the different types of particles by the wet techniques require that the particles be physically separated (density, size, magnetic properties). Microprobe secondary ion mass spectrometry (SIMS) is a technique that can potentially overcome these obstacles by permitting the in situ analysis of POM on single particle surfaces.

2020 ◽  
Author(s):  
Feifei Jia ◽  
Jie Wang ◽  
Yanyan Zhang ◽  
Qun Luo ◽  
Luyu Qi ◽  
...  

<p></p><p><i>In situ</i> visualization of proteins of interest at single cell level is attractive in cell biology, molecular biology and biomedicine, which usually involves photon, electron or X-ray based imaging methods. Herein, we report an optics-free strategy that images a specific protein in single cells by time of flight-secondary ion mass spectrometry (ToF-SIMS) following genetic incorporation of fluorine-containing unnatural amino acids as a chemical tag into the protein via genetic code expansion technique. The method was developed and validated by imaging GFP in E. coli and human HeLa cancer cells, and then utilized to visualize the distribution of chemotaxis protein CheA in E. coli cells and the interaction between high mobility group box 1 protein and cisplatin damaged DNA in HeLa cells. The present work highlights the power of ToF-SIMS imaging combined with genetically encoded chemical tags for <i>in situ </i>visualization of proteins of interest as well as the interactions between proteins and drugs or drug damaged DNA in single cells.</p><p></p>


Langmuir ◽  
2001 ◽  
Vol 17 (23) ◽  
pp. 7332-7338 ◽  
Author(s):  
Jens Lenaerts ◽  
Geert Verlinden ◽  
Luc Van Vaeck ◽  
Renaat Gijbels ◽  
Ingrid Geuens ◽  
...  

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