The toxins bind to the membrane, then finds other toxin molecules around them, forms ring-like structures and punctures a hole in the membrane.
‘Cholesterol present in cells can help pore-forming toxin cytolysin A (ClyA) to puncture nano-sized holes in human or animal cell membranes and kill them.’
Cytolysin A (ClyA) is a type of pore-forming toxin produced by some types of bacteria such as the
Escherichia coli, Shigella and
Salmonella.
The research team studied how a pore-forming toxin called Cytolysin-A (ClyA) works in the bacteria
Escherichia coli. They examined how this toxin forms a ring-like pore composed of 12 protein molecules in the membrane of red blood cells.
"The structure of the toxin is stabilized in the presence of cholesterol, and that is essential for pore formation," said Pradeep Sathyanarayana from the Centre for BioSystems Science and Engineering at IISc and first author of a paper published in the
Proceedings of the National Academy of Sciences.
A
supercomputer and powerful
microscope was used to visualize single molecules of the toxin protein on the membrane. The team found that cholesterol in the cell membrane acted as a
'molecular glue' between neighboring toxin molecules, which plays a significant role in the formation of pores.
"Computer simulations showed that when two pore-forming protein molecules come together, there is a small pocket where the cholesterol goes and interacts with the proteins. So cholesterol provides additional support to hold the two molecules together," said Dr. Roy.
The findings of this study might be helpful in understanding the mechanisms associated with these diseases due to the similarity of these toxins to proteins that cause neurodegenerative disorders such as Alzheimer's and Parkinson's.
Source: Medindia
