2010
DOI: 10.1186/1745-6150-5-38
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Spontaneous chiral symmetry breaking in early molecular networks

Abstract: BackgroundAn important facet of early biological evolution is the selection of chiral enantiomers for molecules such as amino acids and sugars. The origin of this symmetry breaking is a long-standing question in molecular evolution. Previous models addressing this question include particular kinetic properties such as autocatalysis or negative cross catalysis.ResultsWe propose here a more general kinetic formalism for early enantioselection, based on our previously described Graded Autocatalysis Replication Do… Show more

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Cited by 24 publications
(31 citation statements)
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References 87 publications
(130 reference statements)
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“…While for the smaller N max value, the percentage of beneficial outcomes seems to be even higher than for the nominal N max = N G , a larger N max value appears to have a disruptive effect because the system is nearing the equilibrium steady state [23]. This is especially seen for the compotype count and the evolvability score.…”
Section: The Effect Of Assembly Sizementioning
confidence: 75%
See 1 more Smart Citation
“…While for the smaller N max value, the percentage of beneficial outcomes seems to be even higher than for the nominal N max = N G , a larger N max value appears to have a disruptive effect because the system is nearing the equilibrium steady state [23]. This is especially seen for the compotype count and the evolvability score.…”
Section: The Effect Of Assembly Sizementioning
confidence: 75%
“…The GARD model embodies the inheritance of compositional information in the realm of a lipid world scenario for early evolution [20,21,23,27,48,49,51,[55][56][57]. The GARD has recently been pursued in several additional publications [20,39,68,70] and has been chosen as an archetypal metabolism-first realization [68].…”
Section: Resultsmentioning
confidence: 99%
“…One reason for this is that it has been thought that the first biological entities were biopolymers, such as proteins and RNA, rather than lipids; thus, the discussion of homochirality has been mainly limited to biopolymers. The question was examined relatively recently [13,103] (p. 303). The relation between a supramolecular assembly and chirality is complicated compared to biopolymers, and it is necessary to clarify the connection between the features of an amphiphilic molecule and homochirality.…”
Section: Amphiphilic Molecule and Homochiralitymentioning
confidence: 99%
“…The diversity of stereospecific (chiral) phenomena was observed in molecular structures including chirality recognition/sensing [95,96], chirality transfer [97], chirality/helicity induction [98][99][100][101], chirality amplification [102][103][104], chirality breaking [61,105], chirality conflict [106,107], helicity inversion [108][109][110], and chiral phase transitions XVII [111][112][113][114]116]. Progress in the studies of molecular chirality transformation is helpful in resolving three questions.…”
Section: Diversity Of Stereospecific Phenomenamentioning
confidence: 99%