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. 1999 Jun 1;103(11):1547–1560. doi: 10.1172/JCI5549

Figure 6.

Figure 6

Characterization of multiple protein components of LDL exposed to the MPO-H2O2-NO2 system. LDL samples prepared for Figure 5 were analyzed for nitrotyrosine content (a) tryptophan fluorescence (b), unmodified Nε-lysine groups (c), and lipoprotein REM (d), as described in Methods. Under the conditions used, the REM for exhaustively acetylated LDL is 3.8. Data represent the mean ± SD of 3 independent experiments (1 using 125I-labeled LDL as starting material, and 2 using nonlabeled LDL as starting material). + NO2 (filled circles), LDL modified by MPO, an H2O2-generating system (GGOx), and NO2 as described in Figure 5; – NO2 (open circles), LDL modified by MPO and an H2O2-generating system (GGOx) as described in Figure 5.