Study finds how resistant germs transport toxins at molecular level

Berlin [Germany], September 20 (ANI): Micro-organism resistance to antibiotics, in particular, is a major problem in everyday medicine. This has seen the number of resistant microbes increase exponentially.
A recent study published in the journal Nature Communications, says as a result infections that appeared to already have been eradicated using modern drugs now once again pose a potentially fatal threat to humans. The situation is further complicated by the fact that more and more germs are emerging which are resistant to not one but several antibiotics or other drugs.
Research is underway into the mechanisms used by microbes to defend themselves against substances toxic to them. One method is to actively transport the toxic substances out of the cell before they can cause any damage.
Microbes use special membrane transport proteins for this purpose. In particular in eukaryotic microbes such as fungi that have a cell nucleus -- unlike bacteria, which have none -- these membrane proteins are part of the family of ABC transporters ("ATP-binding cassette"). They export the toxic substances by splitting the cellular ATP energy transporter.
Through the study, a German/UK research team headed up by Prof. Dr Lutz Schmitt from the Institute of Biochemistry at HHU has presented the three-dimensional structure of yeast ABC transporter Pdr5 in several functional states. They determined these structures using single-particle cryo-electron microscopy, which makes it possible to examine in particular biological molecules in their natural form at very high resolutions by flash-freezing them to low temperatures.
Not only did the research team show that Pdr5 is a central transport protein in creating the resistance conferred by the membrane protein, but it also used solved structures to localise the drug-binding site and define the transport cycle.
For more than 30 years, Pdr5 has constituted the model for PDR proteins in pathogenic fungi such as Candida albicans, which causes Candidiasis.
The new findings help to explain what it is at the molecular level that enables a single membrane protein to prevent structurally diverse molecules from entering the cell or transport them out of the cell efficiently. The findings can now be used as a basis for designing new drugs in a targeted way to counteract resistance.
For almost 20 years, Professor Schmitt's working group has been conducting research into explaining how the transport protein works. The researchers succeeded in understanding the structure by working together with Prof. Dr Ben Luisi's group in the Department of Biochemistry at Cambridge University.
At HHU, the research also involved the working group of Prof. Dr Holger Gohlke from the Institute of Pharmaceutical and Medicinal Chemistry and the Center for Structural Studies (led by Dr Sander Smits). (ANI)