Literature DB >> 27860220

K-BILDS: A Kinase Substrate Discovery Tool.

D Maheeka Embogama1, Mary Kay H Pflum1.   

Abstract

Kinases catalyze protein phosphorylation to regulate cell signaling events. However, identifying kinase substrates is challenging due to the often low abundance and dynamic nature of protein phosphorylation. Development of novel techniques to identify kinase substrates is necessary. Here, we report kinase-catalyzed biotinylation with inactivated lysates for discovery of substrates (K-BILDS) as a tool to identify direct substrates of a kinase. As a proof of concept, K-BILDS was applied to cAMP-dependent protein kinase A (PKA) with HeLa cell lysates. Subsequent enrichment and MS/MS analysis identified 279 candidate PKA substrates, including 56 previously known PKA substrates. Of the candidate substrates, nuclear autoantigenic sperm protein (NASP), BCL2-associated athanogene 3 (BAG3), and 14-3-3 protein Tau (YWHAQ) were validated as novel PKA substrates. K-BILDS provides a valuable tool to identify direct substrates of any protein kinase.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  ATP-biotin; FSBA; kinase; mass spectrometry; substrate discovery

Mesh:

Substances:

Year:  2016        PMID: 27860220      PMCID: PMC5458359          DOI: 10.1002/cbic.201600511

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  42 in total

Review 1.  Physiological substrates of cAMP-dependent protein kinase.

Authors:  J B Shabb
Journal:  Chem Rev       Date:  2001-08       Impact factor: 60.622

Review 2.  The protein kinase complement of the human genome.

Authors:  G Manning; D B Whyte; R Martinez; T Hunter; S Sudarsanam
Journal:  Science       Date:  2002-12-06       Impact factor: 47.728

Review 3.  Hitting the target: emerging technologies in the search for kinase substrates.

Authors:  Brendan D Manning; Lewis C Cantley
Journal:  Sci STKE       Date:  2002-12-10

4.  Tau-driven 26S proteasome impairment and cognitive dysfunction can be prevented early in disease by activating cAMP-PKA signaling.

Authors:  Natura Myeku; Catherine L Clelland; Sheina Emrani; Nikolay V Kukushkin; Wai Haung Yu; Alfred L Goldberg; Karen E Duff
Journal:  Nat Med       Date:  2015-12-21       Impact factor: 53.440

5.  In-gel digestion for mass spectrometric characterization of proteins and proteomes.

Authors:  Andrej Shevchenko; Henrik Tomas; Jan Havlis; Jesper V Olsen; Matthias Mann
Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

6.  Mammalian histone deacetylase 1 protein is posttranslationally modified by phosphorylation.

Authors:  R Cai; P Kwon; Y Yan-Neale; L Sambuccetti; D Fischer; D Cohen
Journal:  Biochem Biophys Res Commun       Date:  2001-05-04       Impact factor: 3.575

7.  Identification of extracellular signal-regulated kinase 1 (ERK1) direct substrates using stable isotope labeled kinase assay-linked phosphoproteomics.

Authors:  Liang Xue; Pengcheng Wang; Pianpian Cao; Jian-Kang Zhu; W Andy Tao
Journal:  Mol Cell Proteomics       Date:  2014-07-14       Impact factor: 5.911

Review 8.  Protein kinases and phosphatases: the yin and yang of protein phosphorylation and signaling.

Authors:  T Hunter
Journal:  Cell       Date:  1995-01-27       Impact factor: 41.582

9.  Global analysis of phosphorylation networks in humans.

Authors:  Jianfei Hu; Hee-Sool Rho; Robert H Newman; Woochang Hwang; John Neiswinger; Heng Zhu; Jin Zhang; Jiang Qian
Journal:  Biochim Biophys Acta       Date:  2013-03-21

10.  A high-throughput approach for measuring temporal changes in the interactome.

Authors:  Anders R Kristensen; Joerg Gsponer; Leonard J Foster
Journal:  Nat Methods       Date:  2012-08-05       Impact factor: 28.547

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  1 in total

1.  Kinase-Catalyzed Biotinylation to Map Cell Signaling Pathways: Application to Epidermal Growth Factor Signaling.

Authors:  Vindya Ramanayake-Mudiyanselage; D Maheeka Embogama; Mary Kay H Pflum
Journal:  J Proteome Res       Date:  2021-09-07       Impact factor: 5.370

  1 in total

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