scholarly journals Automated analysis of lipid drug-response markers by combined fast and high-resolution whole cell MALDI mass spectrometry biotyping

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
David Weigt ◽  
Denis A. Sammour ◽  
Timon Ulrich ◽  
Bogdan Munteanu ◽  
Carsten Hopf
2020 ◽  
Author(s):  
Mathieu Tiquet ◽  
Raphaël La Rocca ◽  
Daan van Kruining ◽  
Pilar Martinez-Martinez ◽  
Gauthier Eppe ◽  
...  

<p><i>MALDI mass spectrometry imaging (MSI) is a powerful analytical method giving access to the 2D localizations of compounds in a thin section of a sample. To properly discern isobaric compounds in complex biological samples, dynamically harmonized ICR cell (ParaCell©) has been introduce to achieve extreme spectral resolution. However, high resolution MS images realized on a 9.4T FTICR High resolution instrument with recommended parameters suffered from an abnormal shifting of m/z ratios pixel to pixel. Resulting datasets show poor mass accuracy measurements and resolutions under estimations. By following the behavior of the Total Ion Current in function of the number of laser shots, the abnormal mass shifting phenomenon has been linked to the stability of the Total Ion Current (TIC) during images acquisitions. An optimization of laser parameters is proposed in order to limit the observed mass shift to retain machine specifications during MSI analyses. It is also shown that the method has been successfully employed to realize quality MS images with resolution above 1,000,000 in the lipid mass range across the whole image.</i></p>


Talanta ◽  
2018 ◽  
Vol 182 ◽  
pp. 164-170 ◽  
Author(s):  
Kevin Mclean ◽  
Javier Palarea-Albaladejo ◽  
Carol G. Currie ◽  
Lisa H.J. Imrie ◽  
Erin D.T. Manson ◽  
...  

2010 ◽  
Vol 9 (7) ◽  
pp. 3764-3764
Author(s):  
Gisele G. Tomazella ◽  
Idalete daSilva ◽  
Carolina H. Thomé ◽  
Lewis J. Greene ◽  
Christian J. Koehler ◽  
...  

Author(s):  
Mathieu Tiquet ◽  
Raphaël La Rocca ◽  
Daan van Kruining ◽  
Pilar Martinez-Martinez ◽  
Gauthier Eppe ◽  
...  

<p><i>MALDI mass spectrometry imaging (MSI) is a powerful analytical method giving access to the 2D localizations of compounds in a thin section of a sample. To properly discern isobaric compounds in complex biological samples, dynamically harmonized ICR cell (ParaCell©) has been introduce to achieve extreme spectral resolution. However, high resolution MS images realized on a 9.4T FTICR High resolution instrument with recommended parameters suffered from an abnormal shifting of m/z ratios pixel to pixel. Resulting datasets show poor mass accuracy measurements and resolutions under estimations. By following the behavior of the Total Ion Current in function of the number of laser shots, the abnormal mass shifting phenomenon has been linked to the stability of the Total Ion Current (TIC) during images acquisitions. An optimization of laser parameters is proposed in order to limit the observed mass shift to retain machine specifications during MSI analyses. It is also shown that the method has been successfully employed to realize quality MS images with resolution above 1,000,000 in the lipid mass range across the whole image.</i></p>


2012 ◽  
Vol 47 (8) ◽  
pp. 1015-1022 ◽  
Author(s):  
Hisao Shimizu ◽  
Fumihiro Jinno ◽  
Akio Morohashi ◽  
Yuzo Yamazaki ◽  
Masaki Yamada ◽  
...  

2009 ◽  
Vol 113 (15) ◽  
pp. 5891-5894 ◽  
Author(s):  
Jeffrey N. Anker ◽  
W. Paige Hall ◽  
Mary P. Lambert ◽  
Pauline T. Velasco ◽  
Milan Mrksich ◽  
...  

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