Literature DB >> 33659565

A Sensitive Coupled Enzyme Assay for Measuring Kinase and ATPase Kinetics Using ADP-Specific Hexokinase.

Ciaran R McFarlane1, James W Murray2.   

Abstract

Kinases and ATPases perform essential biological functions in metabolism and regulation. Activity of these enzymes is commonly measured by coupling ATP consumption to the synthesis of a detectable product. For most assay systems the ATP concentration during the reaction is unknown, compromising the precision of the assay. Using the ADP-specific hexokinase (ADP-HK) from the thermophilic archaeon Thermococcus litoralis the protocol outlined here allows real time coupling of ATP consumption to downstream signal change enabling accurate kinetic measurements. ADP-HK phosphorylates glucose that is then used by glucose-6-phosphate dehydrogenase to reduce NAD+ to NADH which can be measured at 340 nm. We have shown this assay to be sensitive to the detection of micromole quantities of ADP with no detectable background from ATP.
Copyright © 2020 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  ADP; ADP-specific hexokinase; ATP; ATPase assay; Kinase assay; Kinetics; Michaelis-Menten; Phosphoribulokinase

Year:  2020        PMID: 33659565      PMCID: PMC7842521          DOI: 10.21769/BioProtoc.3599

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  7 in total

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4.  Structural basis for the ADP-specificity of a novel glucokinase from a hyperthermophilic archaeon.

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7.  Structural basis of light-induced redox regulation in the Calvin-Benson cycle in cyanobacteria.

Authors:  Ciaran R McFarlane; Nita R Shah; Burak V Kabasakal; Blanca Echeverria; Charles A R Cotton; Doryen Bubeck; James W Murray
Journal:  Proc Natl Acad Sci U S A       Date:  2019-09-30       Impact factor: 11.205

  7 in total
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