RNAによるアミノ酸の分子非対称性選択の作用機構

  • 田村 浩二
    東京理科大学・基礎工学部・生物工学科 東京理科大学・総合研究機構 科学技術振興機構・さきがけ

書誌事項

タイトル別名
  • MECHANISTIC FEATURES OF RNA-DIRECTED MOLECULAR ASYMMETRY OF AMINO ACIDS
  • RNA ニ ヨル アミノサン ノ ブンシ ヒタイショウセイ センタク ノ サヨウ キコウ

この論文をさがす

抄録

<p>  Chiral-selective aminoacylation of an RNA minihelix (progenitor of the modern tRNA) could provide a crucial clue to solve the origin of homochirality in a biological system. In this reaction, an amino acid donor (aminoacyl phosphate oligonucleotide) is placed in close proximity to minihelix with the help of a bridging oligonucleotide, which possesses sequences complementary to both donor nucleotide and single-stranded NCCA of minihelix, to accomplish the chiral (L-amino acid)-selective aminoacylation of the minihelix. Here, we propose a molecular mechanism of chiral selectivity based on the mutational analysis of the donor and bridging nucleotides. The selectivity for L-amino acids is dependent on the stereochemistry of RNA. Due to cation coordination and sugar pucker, the side chain of D-amino acids is brought much closer to the terminal adenosine of the minihelix, thereby causing steric hindrance of the D-amino acids during amino acid transfer from the donor nucleotide to minihelix. This mechanism completely explains the result of the original chiral-selective aminoacylation experiment without any contradictions. This selective process may have determined the homochirality of L-amino acids in the putative RNA world.</p><p>  </p><p>This article is dedicated to the memory of Dr. Kaoru Harada.</p>

収録刊行物

  • Viva Origino

    Viva Origino 39 (3), 39-44, 2011

    生命の起原および進化学会

関連プロジェクト

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ