Insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.

Aberrant proteins or peptide aggregates form soluble oligomers or nanofibrils that can cause a wide range of amyloidosis diseases, including Alzheimer's disease (AD). The mechanisms of their cytotoxicity, however, remain controversial and poorly understood, greatly hindering the development of...

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Main Authors: Rong Zhou, Bing Xu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4000214?pdf=render
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spelling doaj-f68eb03888404937a594495ccd8383e02020-11-25T00:48:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0194e9575910.1371/journal.pone.0095759Insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.Rong ZhouBing XuAberrant proteins or peptide aggregates form soluble oligomers or nanofibrils that can cause a wide range of amyloidosis diseases, including Alzheimer's disease (AD). The mechanisms of their cytotoxicity, however, remain controversial and poorly understood, greatly hindering the development of AD drugs. Here we report a comprehensive evaluation of the cytotoxicity of the aggregates by meta-analysis. The analysis indicates that the cytotoxicity of the aggregates converges in a narrower range in the mass concentrations than in the molar concentrations, suggesting that it is the weight of the aggregates rather than the number of the molecules that dictates the cytotoxicity. This new perspective implies that these aggregates are likely to have non-specific interactions with cells to cause cell death. The comparison of several existing theories regarding cellular volumes supports that the aggregates may result in crowding effect and increase the free energy, thus resulting in instability of the cells.http://europepmc.org/articles/PMC4000214?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rong Zhou
Bing Xu
spellingShingle Rong Zhou
Bing Xu
Insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.
PLoS ONE
author_facet Rong Zhou
Bing Xu
author_sort Rong Zhou
title Insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.
title_short Insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.
title_full Insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.
title_fullStr Insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.
title_full_unstemmed Insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.
title_sort insight of the cytotoxicity of the aggregates of peptides or aberrant proteins: a meta-analysis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Aberrant proteins or peptide aggregates form soluble oligomers or nanofibrils that can cause a wide range of amyloidosis diseases, including Alzheimer's disease (AD). The mechanisms of their cytotoxicity, however, remain controversial and poorly understood, greatly hindering the development of AD drugs. Here we report a comprehensive evaluation of the cytotoxicity of the aggregates by meta-analysis. The analysis indicates that the cytotoxicity of the aggregates converges in a narrower range in the mass concentrations than in the molar concentrations, suggesting that it is the weight of the aggregates rather than the number of the molecules that dictates the cytotoxicity. This new perspective implies that these aggregates are likely to have non-specific interactions with cells to cause cell death. The comparison of several existing theories regarding cellular volumes supports that the aggregates may result in crowding effect and increase the free energy, thus resulting in instability of the cells.
url http://europepmc.org/articles/PMC4000214?pdf=render
work_keys_str_mv AT rongzhou insightofthecytotoxicityoftheaggregatesofpeptidesoraberrantproteinsametaanalysis
AT bingxu insightofthecytotoxicityoftheaggregatesofpeptidesoraberrantproteinsametaanalysis
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