This question has to deal with amino acids, which are the building blocks of proteins. These amino acids are chiral molecules, a molecule that "lacks an internal plane of symmetry and has a non-superimposable mirror image". (wikipedia) For example, our hands are chiral. They cannot be superimposed on each other, however, they consist of the same 5 fingers and palm.
tonga.usip.edu |
So, why is this important?
In chemistry, when forming these compounds, there is a 50% chance the product will be in the L-configuration and a 50% chance that the product will be in the R-configuration. However, within the human body, there are only L-configured amino acids.
This leads to the big question of "why L-amino acids?"
When prebiotic experiments were performed and electrical discharges were passed through mixtures designed to mimic the chemical composition of the early world's atmosphere, there was a formation of 50% L and 50% R! So now what?
From Rezoan Ratul |
Now just like the different colored tiles Dr. Zappala presented, the L and D amino acids are not compatible with each other. Proteins must be made of 100% L amino acids or 100% D amino acids (these D amino acids, rarely occurring naturally, must be synthesized). There is just no way to make an L and D protein. There would be unacceptable side chain clashes. Furthermore, L amino acids can only act upon other L-configured proteins/molecules. A D-configured protein remains unaffected by the L-configured enzyme. Using this principle, much research has been performed to enhance immune systems, prepare antibiotics, and create long-lasting proteins. crazy.
To end this thought like Dr. Petsko did, with the science fiction writer. Science fiction writers often speculate about parallel universes. If the choice for L-amino acids on our planet was random, then perhaps other universes consist of the opposite. Their molecules may be incompatible with ours. Either way, the mystery of why L was chosen is still up in the air.
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