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. Author manuscript; available in PMC: 2010 Sep 1.

Published in final edited form as: Biochim Biophys Acta. 2009 May 18;1788(9):1901–1906. doi: 10.1016/j.bbamem.2009.05.006

Fig. 6 — Protection of apoLp-III to LDL aggregation. Phospholipase-C was used to induce LDL aggregation, which was measured by the absorbance at 340 nm for 80 min (Panel A, solid line). Incubation of LDL and phospholipase-C in the presence of unmodified apoLp-III (dashed line) provided full protection, while the ability of Ac-apoLp-III (dotted line) to prevent LDL aggregation was reduced. Panel B: LDL and phospholipase-C were incubated with μg quantities of apoLp-III to measure the minimum amount of apoLp-III required to prevent aggregation (measured at 60 min).

Fig. 6 — Protection of apoLp-III to LDL aggregation. Phospholipase-C was used to induce LDL aggregation, which was measured by the absorbance at 340 nm for 80 min (Panel A, solid line). Incubation of LDL and phospholipase-C in the presence of unmodified apoLp-III (dashed line) provided full protection, while the ability of Ac-apoLp-III (dotted line) to prevent LDL aggregation was reduced. Panel B: LDL and phospholipase-C were incubated with μg quantities of apoLp-III to measure the minimum amount of apoLp-III required to prevent aggregation (measured at 60 min).