|
|
|
|
|
by danieltillett
4182 days ago
|
|
I am a microbiologist. It is not that you want to target basic cell structures, but you want to either target multiple systems, or target systems that have a large number of modular interactions. It is relatively easy to create/discover new chemicals that kill bacteria specifically, but if these new chemicals only target one specific component then the bacteria rapidly evolve resistance. All the good antibiotics we have interact with complex systems like ribosomes that are made up of multiple interacting modules. The reason we are having trouble finding new classes of antibiotics is that we are already have chemicals that target most of the interacting and essential cellular modules in bacteria. If you already are targeting 90% of all the possible targets you will find it very hard to discover any new classes of antibiotics. Of course the solution is not to worry too much about finding new classes and just keep tweaking the current antibiotics to keep ahead of the bacteria. The only problem with this strategy is that the economics of antibiotic development is totally broken so the pharmaceutical companies have in the main stopped spending money on finding new antibiotics. What we need to work on is a new way of paying for new antibiotic development. |
|