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Capillary electrophoresis with laser-induced fluorescence detection for ATP quantification in spermatozoa and oocytes
Authors:Angelo Zinellu  Valeria Pasciu  Salvatore Sotgia  Bastianina Scanu  Fiammetta Berlinguer  Giovanni Leoni  Sara Succu  Ignazio Cossu  Eraldo Sanna Passino  Salvatore Naitana  Luca Deiana  Ciriaco Carru
Institution:1. Department Biomedical Sciences and Centre of Excellence for Biotechnology Development and Biodiversity Research, University of Sassari, Viale San Pietro 43/B, 07100, Sassari, Italy
2. Porto Conte Ricerche Srl, Tramariglio, 07041, Alghero, Sassari, Italy
3. Department of Animal Biology, University of Sassari, 07100, Sassari, Italy
4. Equine Reproduction Centre Department of Research for Horses Agris, Agricultural Research Agency of Sardinia, 07100, Sassari, Italy
5. Department of Pathology and Veterinary Clinic, University of Sassari, 07100, Sassari, Italy
Abstract:We describe a new capillary electrophoresis laser-induced fluorescence (CE-LIF) method for the quantification of adenosine 5′-triphosphate (ATP) in spermatozoa and oocytes. The optimization of the precapillary derivatization reaction between ATP and 4,4-difluoro-5,7-dimethyl-4-bora-3a,4adiaza-s-indacene-3-propionyl ethylene diamine hydrochloride (BODIPY FL EDA) has been described. BODIPY-ATP conjugate was analysed in an uncoated fused silica capillary of 75 μm ID and 50 cm effective length using a 10 mmol/L tribasic sodium phosphate buffer, pH 11.5, at 22 kV in <5 min. A good reproducibility of intra- and inter-assay tests was obtained (CV?=?4.55% and 7.14%, respectively). With respect to our previous CE-UV assay, the new method showed an improvement in sensitivity that was about 120-fold (limit of quantification, 0.15 vs 18 μmol/L). Method applicability was proven on the reproductive cells of several animal species (roosters, horses, sheep and goats). Due to the elevated sensitivity, the new assay allows the measurement of adenosine 5′-triphosphate levels from just 20 oocytes. Considering that ATP concentration in reproductive cells is related to the mitochondrial integrity after cryopreservation, the proposed method could be a useful tool in assisted reproductive technologies.
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