Literature DB >> 22713792

Protein aggregation: mechanisms and functional consequences.

Gaetano Invernizzi1, Elena Papaleo, Raimon Sabate, Salvador Ventura.   

Abstract

Understanding the mechanisms underlying protein misfolding and aggregation has become a central issue in biology and medicine. Compelling evidence show that the formation of amyloid aggregates has a negative impact in cell function and is behind the most prevalent human degenerative disorders, including Alzheimer's Parkinson's and Huntington's diseases or type 2 diabetes. Surprisingly, the same type of macromolecular assembly is used for specialized functions by different organisms, from bacteria to human. Here we address the conformational properties of these aggregates, their formation pathways, their role in human diseases, their functional properties and how bioinformatics tools might be of help to study these protein assemblies.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22713792     DOI: 10.1016/j.biocel.2012.05.023

Source DB:  PubMed          Journal:  Int J Biochem Cell Biol        ISSN: 1357-2725            Impact factor:   5.085


  36 in total

1.  Protein Polymerization into Fibrils from the Viewpoint of Nucleation Theory.

Authors:  Dimo Kashchiev
Journal:  Biophys J       Date:  2015-11-17       Impact factor: 4.033

2.  Vector description of electric and hydrophobic interactions in protein homodimers.

Authors:  Angel Mozo-Villarías; Juan Cedano; Enrique Querol
Journal:  Eur Biophys J       Date:  2015-12-11       Impact factor: 1.733

Review 3.  Age-related neurodegenerative diseases.

Authors:  Michael Duggan; Bahareh Torkzaban; Taha Mohseni Ahooyi; Kamel Khalili; Jennifer Gordon
Journal:  J Cell Physiol       Date:  2019-09-25       Impact factor: 6.384

4.  Amyloid cores in prion domains: Key regulators for prion conformational conversion.

Authors:  María Rosario Fernández; Cristina Batlle; Marcos Gil-García; Salvador Ventura
Journal:  Prion       Date:  2017-01-02       Impact factor: 3.931

Review 5.  Molecular and Clinical Aspects of Protein Aggregation Assays in Neurodegenerative Diseases.

Authors:  Anna Villar-Piqué; Matthias Schmitz; Niccolò Candelise; Salvador Ventura; Franc Llorens; Inga Zerr
Journal:  Mol Neurobiol       Date:  2018-02-10       Impact factor: 5.590

6.  Amyloid formation by human carboxypeptidase D transthyretin-like domain under physiological conditions.

Authors:  Javier Garcia-Pardo; Ricardo Graña-Montes; Marc Fernandez-Mendez; Angels Ruyra; Nerea Roher; Francesc X Aviles; Julia Lorenzo; Salvador Ventura
Journal:  J Biol Chem       Date:  2014-10-07       Impact factor: 5.157

7.  Nanodisc-Forming Scaffold Protein Promoted Retardation of Amyloid-Beta Aggregation.

Authors:  Bikash Ranjan Sahoo; Takuya Genjo; Sarah J Cox; Andrea K Stoddard; G M Anantharamaiah; Carol Fierke; Ayyalusamy Ramamoorthy
Journal:  J Mol Biol       Date:  2018-08-28       Impact factor: 5.469

8.  AGGRESCAN3D (A3D): server for prediction of aggregation properties of protein structures.

Authors:  Rafael Zambrano; Michal Jamroz; Agata Szczasiuk; Jordi Pujols; Sebastian Kmiecik; Salvador Ventura
Journal:  Nucleic Acids Res       Date:  2015-04-16       Impact factor: 16.971

9.  Phosphorylation-regulated transitions in an oligomeric state control the activity of the Sae2 DNA repair enzyme.

Authors:  Qiong Fu; Julia Chow; Kara A Bernstein; Nodar Makharashvili; Sucheta Arora; Chia-Fang Lee; Maria D Person; Rodney Rothstein; Tanya T Paull
Journal:  Mol Cell Biol       Date:  2013-12-16       Impact factor: 4.272

Review 10.  Notch3 Signaling and Aggregation as Targets for the Treatment of CADASIL and Other NOTCH3-Associated Small-Vessel Diseases.

Authors:  Dorothee Schoemaker; Joseph F Arboleda-Velasquez
Journal:  Am J Pathol       Date:  2021-04-22       Impact factor: 4.307

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