Fig. 1.
Fig. 1. Kinetics of LD78β processing by CD26/DPP IV. / We incubated 5 μg intact synthetic LD78β at 37°C with 0.1 unit pure soluble CD26/DPP IV in 200 μL of 100 mmol/L Tris (pH 8.5); 20 μL samples were taken at the indicated time-points. The samples were blotted on a PVDF membrane, washed with 0.1% trifluoroacetic acid, and subjected to automated Edman degradation. The molar amounts of intact LD78β (▴), LD78β(3-70) (●), and LD-78β(5-70) (■) present in the samples were calculated from the initial yields of the protein sequencer and are expressed as the percent of the total amount of LD78β.

Kinetics of LD78β processing by CD26/DPP IV.

We incubated 5 μg intact synthetic LD78β at 37°C with 0.1 unit pure soluble CD26/DPP IV in 200 μL of 100 mmol/L Tris (pH 8.5); 20 μL samples were taken at the indicated time-points. The samples were blotted on a PVDF membrane, washed with 0.1% trifluoroacetic acid, and subjected to automated Edman degradation. The molar amounts of intact LD78β (▴), LD78β(3-70) (●), and LD-78β(5-70) (■) present in the samples were calculated from the initial yields of the protein sequencer and are expressed as the percent of the total amount of LD78β.

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