Literature DB >> 6222667

Pyruvate as a fluorescence quencher: a new spectroscopic assay for pyruvate reactions.

T Ando, H Miyata.   

Abstract

Pyruvate ion, which is biologically ubiquitous and participates in many metabolic reactions, was found to be an effective quencher of fluorescence. Compared to other negatively charged quenchers such as I-, pyruvate is not toxic to proteins. By adding an inert, long-lived fluorophore to systems transacting pyruvate, it is possible to estimate activity by measuring the time course of the change in pyruvate quenching of the fluorophore. The procedure is illustrated by measuring the myosin subfragment-1 ATPase activity with a high sensitivity.

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Year:  1983        PMID: 6222667     DOI: 10.1016/0003-2697(83)90065-9

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  3 in total

1.  A continuous fluorimetric assay for ATPase activity.

Authors:  U Banik; S Roy
Journal:  Biochem J       Date:  1990-03-01       Impact factor: 3.857

2.  Mechanistic Analysis of Fluorescence Quenching of Reduced Nicotinamide Adenine Dinucleotide by Oxamate in Lactate Dehydrogenase Ternary Complexes.

Authors:  Huo-Lei Peng; Robert Callender
Journal:  Photochem Photobiol       Date:  2017-06-22       Impact factor: 3.421

3.  Mechanism for Fluorescence Quenching of Tryptophan by Oxamate and Pyruvate: Conjugation and Solvation-Induced Photoinduced Electron Transfer.

Authors:  Huo-Lei Peng; Robert Callender
Journal:  J Phys Chem B       Date:  2018-06-15       Impact factor: 2.991

  3 in total

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