Quantitative and Continuous Analysis of ATP Release from Blood Platelets with Firefly Luciferase Luminescence

Terumasa Higashi; Akio Isomoto; Itiro Tyuma; Eizo Kakishita; Michiko Uomoto; Kiyoyasu Nagai

doi:10.1055/s-0038-1661238

Thrombosis and Haemostasis, Inhaltsverzeichnis

Thromb Haemost 1985; 53(01): 065-069
DOI: 10.1055/s-0038-1661238

Original Article

Schattauer GmbH Stuttgart

Quantitative and Continuous Analysis of ATP Release from Blood Platelets with Firefly Luciferase Luminescence

Authors

Terumasa Higashi

The Department of Physicochemical Physiology, Medical School, Osaka University, Osaka, Japan
Akio Isomoto

The Department of Physicochemical Physiology, Medical School, Osaka University, Osaka, Japan
Itiro Tyuma

The Department of Physicochemical Physiology, Medical School, Osaka University, Osaka, Japan
Eizo Kakishita

^*The Department of Internal Medicine, Hyogo College of Medicine, Hyogo, Japan
Michiko Uomoto

^*The Department of Internal Medicine, Hyogo College of Medicine, Hyogo, Japan
Kiyoyasu Nagai

^*The Department of Internal Medicine, Hyogo College of Medicine, Hyogo, Japan

Abstract

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Summary

An analytical method was devised to determine the entire course of the adenosine-triphosphate (ATP) release from blood platelets based on a continuous measurement of firefly luciferase luminescence. The equation of the release reaction was derived after due consideration of substrate (ATP) consumption and product (oxyluciferin) inhibition on the luciferase reaction as follows: C, = v_t × (K_m/V_max) × (I + I_t/K_i) + I_t where C_t is the total concentration of the released ATP at time t, v_t is the velocity of the luciferase reaction at time t and is directly measured, I_t is the concentration of oxyluciferin at time t, and V_max, K_m and K_i are constants. C, of the gel-filtered platelet suspension (GFP) could be determined by substituting v_t and I_t as functions of t. The effects of albumin and temperature on the reaction were also studied.

Key words

ATP release from blood platelets - Firefly luciferase luminescence - Time-course kinetics - Product inhibition

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Referenzen

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