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. 2014 Aug 28;289(41):28249–28259. doi: 10.1074/jbc.M114.589002

FIGURE 4.

FIGURE 4.

ApoA-I epitope identification using digestion at lysine residues. A, chromatogram of LysC-derived peptides fractionation by reversed phase-high performance liquid chromatography. B and C, immunoreactivity of autoantibodies from positive patient sera (B) and negative patient sera (C) against peptides present in each collected fraction, and against the synthetic peptides A and B. D and E, chromatogram of the immunoreactive fraction 70 (D) and fraction 71 (E) by nano-liquid chromatography system. F and G, representative mass spectra of the peptide A (F) and peptide B (G) present in immunoreactive fractions by mass spectrometry (LTQ/Orbitrap). Relative error = (Mexperimental − Mcalculated)/Mcalculated. Positive or negative sera: samples previously classified as containing high-titers or low titers of anti-apoA-I IgG, respectively.