Literature DB >> 20155977

Direct quantification of protein-metal ion affinities by electrospray ionization mass spectrometry.

Lu Deng, Nian Sun, Elena N Kitova, John S Klassen.   

Abstract

The application of the direct electrospray ionization mass spectrometry (ES-MS) assay for quantifying the stoichiometry and absolute affinity of protein-metal ion binding in vitro is described. Control ES-MS experiments performed on solutions containing calcium chloride or calcium acetate and a pair of proteins that do not bind calcium ions in solution revealed that the nonspecific association of metal ions to proteins during ES is a random process, independent of protein size and structure. These results establish the reliability of the reference protein method for quantitatively correcting ES mass spectra for the occurrence of nonspecific metal ion binding to proteins during ES-MS analysis. To demonstrate the utility of the direct ES-MS assay, when carried out using the reference protein method, the calcium binding stoichiometry of bovine alpha-lactalbumin and the calcium ion affinity of bovine beta-lactoglobulin were established.

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Year:  2010        PMID: 20155977     DOI: 10.1021/ac902633d

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  12 in total

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4.  N-terminal region of CusB is sufficient for metal binding and metal transfer with the metallochaperone CusF.

Authors:  Tiffany D Mealman; Mowei Zhou; Trisiani Affandi; Kelly N Chacón; Mariana E Aranguren; Ninian J Blackburn; Vicki H Wysocki; Megan M McEvoy
Journal:  Biochemistry       Date:  2012-08-17       Impact factor: 3.162

5.  Quantifying protein-carbohydrate interactions using liquid sample desorption electrospray ionization mass spectrometry.

Authors:  Yuyu Yao; Km Shams-Ud-Doha; Rambod Daneshfar; Elena N Kitova; John S Klassen
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8.  mebipred: identifying metal binding potential in protein sequence.

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Journal:  Bioinformatics       Date:  2022-05-27       Impact factor: 6.931

9.  Phosphorylation of α-Synuclein at Y125 and S129 alters its metal binding properties: implications for understanding the role of α-Synuclein in the pathogenesis of Parkinson's Disease and related disorders.

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Journal:  ACS Chem Neurosci       Date:  2011-09-14       Impact factor: 4.418

10.  Difference in the binding mechanism of distinct antimony forms in bovine serum albumin.

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Journal:  Biometals       Date:  2021-02-15       Impact factor: 2.949

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