posted on 2020-09-28, 17:34authored byLise Bedoin, Sandra Alves, Jean-François Lambert
In current living matter, biopolymers
follow specific sequences
that give them special properties, such as the sequence of amino acids
(AAs) in proteins and peptides. A major challenge for the elucidation
of the origins of life lies in understanding how, for example, nonrandom
polypeptides have been selected among all the possible ones. While
many investigations established plausible prebiotic polymerization
pathways, surprisingly, only a few attempted to study the selectivity
of these processes. We studied a mineral surface polymerization scenario
based on moderate thermal activation of leucine + glutamic acid mixtures
on silica. Oligopeptides up to octamers were quantitatively formed
in a “clean” prebiotic reaction and analyzed by high-resolution
mass spectrometry and Fourier transform ion cyclotron resonance spectrometry
for unambiguous molecular assignments. Nontrivial oligomerization
selectivities are evidenced in both stoichiometric compositions and
AA sequences, while comparable selectivities are not observed in other
polymerization scenarios. This must therefore be due to specific catalytic
reaction pathways occurring on the SiO2 surface. A statistical
measure of information contained in oligopeptide distributions is
proposed. It could be used to follow the evolution of potentially
meaningful complexity in biopolymers from the mineral to the biochemical
world.