New Discoveries In Cell Aging
Main Category: GeneticsAlso Included In: Biology / Biochemistry; Alzheimer's / Dementia
Article Date: 25 Jan 2012 - 0:00 PST
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A group of researchers led by the Institute of Biotechnology and Biomedicine (IBB) and Universitat Autonoma de Barcelona (UAB) can now quantify with precision the effect of protein aggregation on cell aging processes using Escherichia coli bacteria and the molecule which triggers Alzheimer's disease as models. Scientists demonstrated that the effect can be predicted before it occurs. Protein aggregation is related to several diseases, including neurodegenerative diseases.
The research, published recently in the Journal of Molecular Biology, provides an extremely reliable system with which to model and quantify the effect of protein aggregation on the viability, division and aging of cells. It also aids in further understanding the natural evolution of proteins. According to Salvador Ventura, researcher at IBB and director of the research project, "it will serve to develop computer approximations to predict the effects aggregation has on cell aging, as well as to search for molecules that act as natural chaperones, highly conserved proteins which are present also in humans and which have the ability to reduce this effect in the bacteria".
Although it is widely accepted that bad folding and aggregation of proteins reduces the cell's ability to survive and reproduce, the damage caused had not been previously measured experimentally as precisely as it was in this research.
In previous studies scientists had verified that the expression of the Alzheimer's AB42 peptide in bacteria induces the process of protein aggregation. Now they have demonstrated that this effect is coded in the protein aggregation sequence and that it depends on intrinsic properties, not on a direct response from within the cell. This makes it possible to predict the effect. Scientists also demonstrated that damage caused to the bacteria is controlled by molecular chaperones, which reduce the tendency of proteins to aggregate and favour cell survival.
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Universitat Autonoma de Barcelona
MLA
23 Feb. 2012. <http://www.medicalnewstoday.com/releases/240688.php>
APA
http://www.medicalnewstoday.com/releases/240688.php.
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