Literature DB >> 15494146

Kinetics of an enzyme-catalyzed reaction measured by electrospray ionization mass spectrometry using a simple rapid mixing attachment.

Paul V Attwood1, Michael A Geeves.   

Abstract

Mass spectrometry offers a potential means of measuring virtually all enzyme-catalyzed reactions by simultaneously measuring the concentrations of substrates, products, and intermediates where there are differences in mass between them. To perform these measurements the reaction mixture must be aged for different times and then ionized. Electrospray ionization mass spectrometry provides the most direct means of measuring these reactions. Here we describe a simple reaction mixing and ageing attachment for an electrospray ionization mass spectrometer, built from commercially available components. We have employed this device to measure the kinetics of a model reaction, namely the hydrolysis of N2-(carbobenzyloxy)-L-lysine-p-nitrophenyl ester-catalyzed by trypsin. In this way we were able to measure the kinetics of substrate depletion, product formation, and changes in both free enzyme and acyl-enzyme intermediate concentration in the approach to steady state. With this device we were able to measure reaction times down to about 640 ms.

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Year:  2004        PMID: 15494146     DOI: 10.1016/j.ab.2004.08.010

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


  5 in total

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Authors:  Anne Roberts; Cristina Furdui; Karen S Anderson
Journal:  Rapid Commun Mass Spectrom       Date:  2010-07-15       Impact factor: 2.419

2.  Monitoring the dynamics of monomer exchange using electrospray mass spectrometry: the case of the dimeric glucosamine-6-phosphate synthase.

Authors:  Guillaume Chevreux; Cédric Atmanene; Philippe Lopez; Jamal Ouazzani; Alain Van Dorsselaer; Bernard Badet; Marie-Ange Badet-Denisot; Sarah Sanglier-Cianférani
Journal:  J Am Soc Mass Spectrom       Date:  2011-01-15       Impact factor: 3.109

3.  Monitoring enzyme reaction and screening of inhibitors of acetylcholinesterase by quantitative matrix-assisted laser desorption/ionization Fourier transform mass spectrometry.

Authors:  Zhe Xu; Shengjun Yao; Yuanlong Wei; Jing Zhou; Li Zhang; Cuihong Wang; Yinlong Guo
Journal:  J Am Soc Mass Spectrom       Date:  2008-08-15       Impact factor: 3.109

4.  Mass spectrometry-based monitoring of millisecond protein-ligand binding dynamics using an automated microfluidic platform.

Authors:  Yongzheng Cong; Shanta Katipamula; Cameron D Trader; Daniel J Orton; Tao Geng; Erin S Baker; Ryan T Kelly
Journal:  Lab Chip       Date:  2016-04-26       Impact factor: 6.799

5.  Studying biomolecular folding and binding using temperature-jump mass spectrometry.

Authors:  Adrien Marchand; Martin F Czar; Elija N Eggel; Jérôme Kaeslin; Renato Zenobi
Journal:  Nat Commun       Date:  2020-01-28       Impact factor: 14.919

  5 in total

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