Regulating neuronal membrane lipids could be the key to Alzheimer’s and Parkinson’s
This news release is available in Spanish.
A study published in the prestigious journal Scientific Reports from the Nature group demonstrates, for the first time and using computational tools, that polyunsaturated lipids can alter the binding rate of two types of receivers involved in certain nervous system diseases. The work was led by members of the Research Programme on Biomedical Informatics at the IMIM (Hospital del Mar Medical Research Institute) and Pompeu Fabra University as well as researchers from the University of Tampere (Finland), and also involved scientists from the University of Barcelona.
Using latest-generation molecular simulations, which are like "computational microscopes", the researchers have demonstrated that a decrease in polyunsaturated lipids in neuronal membranes, as seen in Parkinson's and Alzheimer's sufferers, directly affects the binding rate of dopamine and adenosine receptors. These are part of the family of receptors connected to the G protein (GPCR), located in the cell membrane and responsible for transmitting signals to within the cell. Until now, various studies have demonstrated that lipid profiles in the brains of people with diseases like Alzheimer's and Parkinson's are very different from those of healthy people. These studies showed that the levels of a polyunsaturated fatty acid in neuronal membranes are considerably lower in the brains of sufferers. The researchers believe that this difference in the lipid composition of membranes could alter the way in which certain proteins interact with each other, as in the case of the GPCR receivers.
According to Jana Selent, a researcher from the PharmacoInformatics group at the IMIM and UPF "It has recently been discovered that the protein complex formed by the binding of dopamine and adenosine receivers, two key GPCRs in diverse cerebral processes, could be a potential therapeutic target in neurodegenerative diseases like Parkinson's and Alzheimer's. Our study suggests that polyunsaturated lipids like DHA are able to modulate the speed at which this protein complex forms, and that could in turn affect its function".
The researchers used latest-generation molecular simulation techniques that allow them to observe, almost at the atomic level, biological dynamics that cannot be described with experimental techniques. Until relatively recently, it was not possible to conduct molecular simulations of this magnitude. However, this field has undergone an important evolution over the past few years, thanks to new breakthroughs in both hardware and software. "In this way, taking advantage of the latest technology in the field of biocomputation, we have been able to simulate the binding dynamics of these two receptors in distinct lipid membranes, an important biological scenario for nervous system diseases", explains Ramon Guixà González, a researcher currently affiliated with the Charité Hospital in Berlin and co-author of this study.
These results will enable, in the future, new therapeutic pathways to be initiated for regulating the binding of these receivers, either through the lipid composition of the membrane or by designing new lipids that have a modulating effect on this binding rate. It will also facilitate the study of other similar scenarios where specific membrane lipids are able to modulate the behaviour of other important receivers, at a clinical level. Even so, the researchers say the most important short-term challenge is looking at the real impact of reducing or increasing the formation speed of this protein complex on the cell function where it is expressed.
Ramon Guixà-González, Matti Javanainen, Maricel Gómez-Soler, Begoña Cordobilla, Joan Carles Domingo, Ferran Sanz, Manuel Pastor, Francisco Ciruela, Hector Martinez-Seara, Jana Selent. Membrane omega-3 fatty acids modulate the oligomerisation kinetics of adenosine A2A and dopamine D2 receptors Membrane levels of docosahexaenoic acid. 2016 Scientific Reports 6:19839. (http://www.nature.com/articles/srep19839)
Marta Calsina Freixas