RNA affinity for molecular L-histidine; genetic code origins

Selection for affinity for free histidine yields a single RNA aptamer, which was isolated 54 times independently. This RNA is highly specific for the side chain and binds protonated L-histidine with 10(2)-10(3)-fold stereoselectivity and a dissociation constant (K(D)) of 8-54 microM in different iso...

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Veröffentlicht in:Journal of molecular evolution 2005-08, Vol.61 (2), p.226-235
Hauptverfasser: Majerfeld, Irene, Puthenvedu, Deepa, Yarus, Michael
Format: Artikel
Sprache:eng
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Zusammenfassung:Selection for affinity for free histidine yields a single RNA aptamer, which was isolated 54 times independently. This RNA is highly specific for the side chain and binds protonated L-histidine with 10(2)-10(3)-fold stereoselectivity and a dissociation constant (K(D)) of 8-54 microM in different isolates. These histidine-binding RNAs have a common internal loop-hairpin loop structure, based on a conserved RAAGUGGGKKN(0-36) AUGUN(0-2)AGKAACAG sequence. Notably, the repetitively isolated sequence contains two histidine anticodons, both implicated by conservation and chemical data in amino acid affinity. This site is probably the simplest structure that can meet our histidine affinity selection, which strengthens experimental support for a "stereochemical" origin of the genetic code.
ISSN:0022-2844
1432-1432
DOI:10.1007/s00239-004-0360-9