In situ analysis of organic monolayers and their reactivity on single micrometer-sized particles by time-of-flight secondary ion mass spectrometry

Author(s):  
Thomas F. Fister ◽  
Gregory S. Strossman ◽  
Kristie L. Willett ◽  
Robert W. Odom ◽  
Richard W. Linton
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>


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

<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 <a></a><a>photon, electron or X-ray</a> 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 <a>chemical</a> tag into the protein <i>via</i> genetic code expansion technique. The method was developed and validated by imaging GFP in <i>E. coli</i> and human HeLa cancer cells, and then utilized to visualize the distribution of chemotaxis protein CheA in <i>E. Coli</i> 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.<br></p>


2002 ◽  
Vol 74 (16) ◽  
pp. 4011-4019 ◽  
Author(s):  
Thomas P. Roddy ◽  
Donald M. Cannon ◽  
Chad A. Meserole ◽  
Nicholas Winograd ◽  
Andrew G. Ewing

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>


Author(s):  
M. P. Mawn ◽  
R. W. Linton ◽  
A. Benninghoven

When coupled to a time-of-flight (TOF) mass analyzer which provides a high transmission, quasi-simultaneous detection of secondary ions, and theoretically unlimited mass range, secondary ion mass spectrometry (SIMS) is well suited for submonolayer molecular analysis of solid surfaces. Additionally, molecular ion images may be obtained by using a focused primary ion beam rastered on the sample surface to provide lateral distributions of chemical species.TOF-SIMS has been shown effective at characterizing low level polymer additives such as UV absorbers, thermal stabilizers, anti-oxidants, and slip agents in polymer extracts deposited on roughened Ag substrates. Additionally, in-situ analysis of linear low density polyethylene (LLDPE) samples using TOF-SIMS has provided information on surface segregation and surface oxidation. The polymer extract analysis has the advantage of both preconcentrating the polymer additives, as well as providing enhanced ion yields through Ag canonization. However, the in-situ analysis is also a valuable approach since it alleviates the time consuming extraction procedure and provides information on additive surface segregation and oxidation.


Sign in / Sign up

Export Citation Format

Share Document