Literature DB >> 15544951

Quality control of integral membrane proteins.

Mark P Krebs1, Syed M Noorwez, Ritu Malhotra, Shalesh Kaushal.   

Abstract

Integral membrane proteins (IMPs) are essential components of the plasma and organellar membranes of the eukaryotic cell. Non-native IMPs, which can arise as a result of mutations, errors during biosynthesis or cellular stress, can disrupt these membranes and potentially lead to cell death. To protect against this outcome, the cell possesses quality control (QC) systems that detect and dispose of non-native IMPs from cellular membranes. Recent studies suggest that recognition of non-native IMPs by the QC machinery is correlated with the thermodynamic stability of these proteins. Consistent with this, small molecules known as chemical and pharmacological chaperones have been identified that stabilize non-native IMPs and enable them to evade QC. These findings have far-reaching implications for treating human diseases caused by defective IMPs.

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Year:  2004        PMID: 15544951     DOI: 10.1016/j.tibs.2004.10.009

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  16 in total

1.  Design of improved membrane protein production experiments: quantitation of the host response.

Authors:  Nicklas Bonander; Kristina Hedfalk; Christer Larsson; Petter Mostad; Celia Chang; Lena Gustafsson; Roslyn M Bill
Journal:  Protein Sci       Date:  2005-07       Impact factor: 6.725

Review 2.  Protein misfolding and retinal degeneration.

Authors:  Radouil Tzekov; Linda Stein; Shalesh Kaushal
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-11-01       Impact factor: 10.005

3.  FXYD proteins stabilize Na,K-ATPase: amplification of specific phosphatidylserine-protein interactions.

Authors:  Neeraj Kumar Mishra; Yoav Peleg; Erica Cirri; Talya Belogus; Yael Lifshitz; Dennis R Voelker; Hans-Juergen Apell; Haim Garty; Steven J D Karlish
Journal:  J Biol Chem       Date:  2011-01-12       Impact factor: 5.157

Review 4.  Chaperoning G protein-coupled receptors: from cell biology to therapeutics.

Authors:  Ya-Xiong Tao; P Michael Conn
Journal:  Endocr Rev       Date:  2014-03-24       Impact factor: 19.871

5.  Evidence that proteosome inhibitors and chemical chaperones can rescue the activity of retinol dehydrogenase 12 mutant T49M.

Authors:  Seung-Ah Lee; Olga V Belyaeva; Natalia Y Kedishvili
Journal:  Chem Biol Interact       Date:  2011-01-11       Impact factor: 5.192

Review 6.  Misfolded proteins and retinal dystrophies.

Authors:  Jonathan H Lin; Matthew M Lavail
Journal:  Adv Exp Med Biol       Date:  2010       Impact factor: 2.622

7.  Conserved disulfide bond is not essential for the adenosine A2A receptor: Extracellular cysteines influence receptor distribution within the cell and ligand-binding recognition.

Authors:  Andrea N Naranjo; Amy Chevalier; Gregory D Cousins; Esther Ayettey; Emily C McCusker; Carola Wenk; Anne S Robinson
Journal:  Biochim Biophys Acta       Date:  2014-11-16

8.  The peripheral neuropathy-linked Trembler and Trembler-J mutant forms of peripheral myelin protein 22 are folding-destabilized.

Authors:  Jeffrey K Myers; Charles K Mobley; Charles R Sanders
Journal:  Biochemistry       Date:  2008-09-17       Impact factor: 3.162

Review 9.  Monotopic Membrane Proteins Join the Fold.

Authors:  Karen N Allen; Sonya Entova; Leah C Ray; Barbara Imperiali
Journal:  Trends Biochem Sci       Date:  2018-10-15       Impact factor: 13.807

10.  N-glycans are direct determinants of CFTR folding and stability in secretory and endocytic membrane traffic.

Authors:  Rina Glozman; Tsukasa Okiyoneda; Cory M Mulvihill; James M Rini; Herve Barriere; Gergely L Lukacs
Journal:  J Cell Biol       Date:  2009-03-23       Impact factor: 10.539

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