Publications by authors named "J L Romson"

There is need for well-defined lignin macromolecules for research related to their use in biomaterial and biochemical applications. Lignin biorefining efforts are therefore under investigation to meet these needs. The detailed knowledge of the molecular structure of the native lignin and of the biorefinery lignins is essential for understanding the extraction mechanisms as well as chemical properties of the molecules.

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Rationale: Chemical mass shifts in quadrupolar ion traps have been studied previously but only for a limited number of analytes and mass ranges. Here, mass shifts of cluster ions, commonly used as calibrants, and other analytes are qualitatively evaluated on the Bruker amaZon spherical ion trap (QIT) and the Finnigan LXQ linear ion trap (LIT). To extend the mass range from previous experiments m/z up to 4000 are investigated.

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Rationale: A calibration solution for mass spectrometry needs to cover the range of interest with intense and sufficiently narrowly spaced peaks. Limited options fulfilling this may lead to compromises between performance and ease of use. SpheriCal -ESI was designed to combine high calibration performance for electrospray ionization (ESI) mass spectrometric analysis of peptides in positive mode with quick and easy use.

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Article Synopsis
  • Osteopontin is a protein secreted by osteoblasts that plays a role in bone diseases, cancers, and inflammation due to its ability to bind various molecules.
  • DEAE-Cibacron blue 3GA was utilized to extract recombinant osteopontin from human plasma, effectively removing major abundant proteins without using antibodies.
  • The process involved using specific buffer systems to separate osteopontin from other proteins, which was later identified using MALDI-TOF MS/MS after digestion with trypsin.
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A method for off-line CE-MALDI-TOF-MS and MS, and on-target digestion under a fluorocarbon lid was developed and applied for the analysis of proteins in the spermatophore of the butterfly Pieris napi. Fractionation revealed many peptides otherwise not detected or resolved. Automated fractionation was performed with an in-lab developed robotic system, and automated on-target tryptic digestion under a fluorocarbon lid was demonstrated with the same system.

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