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Figure 1 | Arthritis Research & Therapy

Figure 1

From: Implication of granulocyte-macrophage colony-stimulating factor induced neutrophil gelatinase-associated lipocalin in pathogenesis of rheumatoid arthritis revealed by proteome analysis

Figure 1

Detection of trypsin digested peptides from granulocyte-macrophage colony-stimulating factor (GM-CSF) stimulated neutrophils by matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS). Neutrophils, treated with GM-CSF or untreated, were divided into four subcellular fractions: cytosol, membrane/organelle, nuclei and cytoskeleton. Then, proteins were extracted from each fraction and digested by trypsin. The produced peptides, concentrated by Ziptip C18, were placed together with a bradykinin peptide (m/z of 757) as an internal control on a chip of the MALDI-TOF MS. Representative spectra from 900 to 1,500 m/z are shown in each of the four fractions.

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