Literature DB >> 3434797

Protein kinase assay by paper-trichloroacetic acid method: high performance using phosphocellulose paper and washing an ensemble of samples on flat sheets.

D Sahal1, Y Fujita-Yamaguchi.   

Abstract

Phosphocellulose paper has been found to be the paper of choice in assaying protein kinase activities using [gamma-32P]ATP by the trichloroacetic acid method of precipitation and washing. A study of binding of ATP of increasing concentrations at constant specific activity with Whatman 3MM or ATP-coated Whatman 3 MM papers (in vogue) versus phosphocellulose paper (proposed here) has shown that the latter has the least affinity for ATP when washing is done with either trichloracetic acid or trichloroacetic acid containing pyrophosphate. In an experiment where the placental cytosolic protein kinase was serially diluted, the phosphocellulose paper was found to give higher signal/noise ratios at all dilutions studied compared to the other two papers. With regard to the technological side of washing the papers, we have found that the traditional method of cutting papers into small squares before loading the samples is perhaps not the best. Instead, we propose the use of a flat sheet matrix for loading the samples because this method ensures uniformity of washing among the samples while shaking is performed on a simple shaker. In addition, the whole paper matrix can provide an almost instantaneous autoradiogram of hundreds of samples facilitating biochemical experimentation with protein kinases.

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Year:  1987        PMID: 3434797     DOI: 10.1016/0003-2697(87)90129-1

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


  9 in total

1.  Increased endothelial albumin permeability mediated by protein kinase C activation.

Authors:  J J Lynch; T J Ferro; F A Blumenstock; A M Brockenauer; A B Malik
Journal:  J Clin Invest       Date:  1990-06       Impact factor: 14.808

2.  Protein kinase activities during early development of Ascaris suum.

Authors:  C Seidl; K B Moritz
Journal:  Naturwissenschaften       Date:  1990-10

3.  Immobilized glucose-6-phosphate dehydrogenase as a substrate for solubilized epidermal growth factor receptor tyrosine kinase. A convenient microtiter plate assay system.

Authors:  C H Cheng; S T Hui
Journal:  Appl Biochem Biotechnol       Date:  1996-02       Impact factor: 2.926

4.  An enzyme-linked immunosorbent assay for the determination of src-family tyrosine kinase activity in breast cancer.

Authors:  G Rijksen; S S Adriaansen-Slot; G E Staal
Journal:  Breast Cancer Res Treat       Date:  1996       Impact factor: 4.872

5.  Insulin receptor function is inhibited by guanosine 5'-[gamma-thio]triphosphate (GTP[S]).

Authors:  H W Davis; J M McDonald
Journal:  Biochem J       Date:  1990-09-01       Impact factor: 3.857

6.  Insulin-stimulated phosphorylation of calmodulin.

Authors:  D B Sacks; H W Davis; D L Crimmins; J M McDonald
Journal:  Biochem J       Date:  1992-08-15       Impact factor: 3.857

7.  Annexin 5 as a potential regulator of annexin 1 phosphorylation by protein kinase C. In vitro inhibition compared with quantitative data on annexin distribution in human endothelial cells.

Authors:  P Raynal; F Hullin; J M Ragab-Thomas; J Fauvel; H Chap
Journal:  Biochem J       Date:  1993-06-15       Impact factor: 3.857

8.  Stimulation by ATP-Mg2+ and inactivation by cyclic-AMP-dependent phosphorylation of a cytosolic monkey brain aminopeptidase.

Authors:  S Ramamoorthy; A S Balasubramanian
Journal:  Biochem J       Date:  1989-03-15       Impact factor: 3.857

9.  Determination of AMP-activated protein kinase phosphorylation sites in recombinant protein expressed using the pET28a vector: a cautionary tale.

Authors:  Bernhard Renz; Joanna K Davies; David Carling; Hugh Watkins; Charles Redwood
Journal:  Protein Expr Purif       Date:  2009-03-06       Impact factor: 1.650

  9 in total

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