RNA scaffolds for minihelix-based aminoacyl transfer: Design of "transpeptizymes"

Citation
Ny. Sardesai et al., RNA scaffolds for minihelix-based aminoacyl transfer: Design of "transpeptizymes", J BIO STRUC, 2000, pp. 29-37
Citations number
52
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
ISSN journal
07391102 → ACNP
Year of publication
2000
Pages
29 - 37
Database
ISI
SICI code
0739-1102(2000):S1<29:RSFMAT>2.0.ZU;2-2
Abstract
Some evidence and considerations suggest that RNA minihelices based on the acceptor-T PsiC stem-loop of tRNAs are the historical, more ancient part of the tRNA structure. These minihelices are substrates for aminoacylation by tRNA synthetases. In the transition from the RNA world to the theatre of p roteins, aminoacyl minihelices may have had a role in early systems of pept ide synthesis. Such systems would require bringing together aminoacyl group s into close proximity in order for peptide bonds to form. Here we report t he design of RNA scaffolds based on pieces of the structure of the P4-P6 do main of the Tetrahymena ribozyme. RNA minihelices were incorporated into th ese scaffolds and the resulting RNAs could be enzymatically aminoacylated. The RNA scaffolds containing the minihelix-like pieces associated spontaneo usly to create the presumptive P4-P6 structure and thereby bring together t he substrates for aminoacylation. Thus, peptide synthesis with associating RNA scaffolds that contain minihelix-like motifs appears plausible.