Literature DB >> 26278914

Regulation of Proteasomal Degradation by Modulating Proteasomal Initiation Regions.

Kazunobu Takahashi1, Andreas Matouschek2,3, Tomonao Inobe1.   

Abstract

Methods for regulating the concentrations of specific cellular proteins are valuable tools for biomedical studies. Artificial regulation of protein degradation by the proteasome is receiving increasing attention. Efficient proteasomal protein degradation requires a degron with two components: a ubiquitin tag that is recognized by the proteasome and a disordered region at which the proteasome engages the substrate and initiates degradation. Here we show that degradation rates can be regulated by modulating the disordered initiation region by the binding of modifier molecules, in vitro and in vivo. These results suggest that artificial modulation of proteasome initiation is a versatile method for conditionally inhibiting the proteasomal degradation of specific proteins.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 26278914      PMCID: PMC4922138          DOI: 10.1021/acschembio.5b00554

Source DB:  PubMed          Journal:  ACS Chem Biol        ISSN: 1554-8929            Impact factor:   5.100


  30 in total

1.  A ubiquitin-based tagging system for controlled modulation of protein stability.

Authors:  J H Stack; M Whitney; S M Rodems; B A Pollok
Journal:  Nat Biotechnol       Date:  2000-12       Impact factor: 54.908

2.  Concurrent translocation of multiple polypeptide chains through the proteasomal degradation channel.

Authors:  Cheolju Lee; Sumit Prakash; Andreas Matouschek
Journal:  J Biol Chem       Date:  2002-06-21       Impact factor: 5.157

3.  Mammalian cell-based optimization of the biarsenical-binding tetracysteine motif for improved fluorescence and affinity.

Authors:  Brent R Martin; Ben N G Giepmans; Stephen R Adams; Roger Y Tsien
Journal:  Nat Biotechnol       Date:  2005-09-11       Impact factor: 54.908

4.  Specific covalent labeling of recombinant protein molecules inside live cells.

Authors:  B A Griffin; S R Adams; R Y Tsien
Journal:  Science       Date:  1998-07-10       Impact factor: 47.728

Review 5.  Disordered proteinaceous machines.

Authors:  Monika Fuxreiter; Ágnes Tóth-Petróczy; Daniel A Kraut; Andreas Matouschek; Andreas T Matouschek; Roderick Y H Lim; Bin Xue; Lukasz Kurgan; Vladimir N Uversky
Journal:  Chem Rev       Date:  2014-04-04       Impact factor: 60.622

Review 6.  Recent progress in generating intracellular functional antibody fragments to target and trace cellular components in living cells.

Authors:  Philipp D Kaiser; Julia Maier; Bjoern Traenkle; Felix Emele; Ulrich Rothbauer
Journal:  Biochim Biophys Acta       Date:  2014-05-02

Review 7.  Aberrant rel/nfkb genes and activity in human cancer.

Authors:  B Rayet; C Gélinas
Journal:  Oncogene       Date:  1999-11-22       Impact factor: 9.867

8.  Proteasomes can degrade a significant proportion of cellular proteins independent of ubiquitination.

Authors:  James M Baugh; Ekaterina G Viktorova; Evgeny V Pilipenko
Journal:  J Mol Biol       Date:  2009-01-08       Impact factor: 5.469

9.  Beyond natural antibodies: the power of in vitro display technologies.

Authors:  Andrew R M Bradbury; Sachdev Sidhu; Stefan Dübel; John McCafferty
Journal:  Nat Biotechnol       Date:  2011-03       Impact factor: 54.908

10.  Defining the geometry of the two-component proteasome degron.

Authors:  Tomonao Inobe; Susan Fishbain; Sumit Prakash; Andreas Matouschek
Journal:  Nat Chem Biol       Date:  2011-01-30       Impact factor: 15.040

View more
  1 in total

1.  Substrate Ubiquitination Controls the Unfolding Ability of the Proteasome.

Authors:  Eden L Reichard; Giavanna G Chirico; William J Dewey; Nicholas D Nassif; Katelyn E Bard; Nickolas E Millas; Daniel A Kraut
Journal:  J Biol Chem       Date:  2016-07-12       Impact factor: 5.157

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.