Abstract

Soria Baouz1, Anne Woisard1, Lila Chenoune, Gustave Aguié, Gérard Keith, JeanMarie Schmitter, Jean-Pierre Le Caer and Codjo Hountondji

Periodate-oxidized tRNA (tRNAox), the 2’,3’-dialdehyde derivative of tRNA, was used as a zero-length active sitedirected affinity labeling reagent, to covalently label proteins at the peptidyl transferase center (PTC), the catalytic site of the large ribosomal subunit. When human 80S or Escherichia coli 70S ribosomes were reacted separately with tRNAox positioned at the P-site, in the presence of an appropriate 12 mer mRNA, a set of two tRNAox- labeled ribosomal proteins was observed. These proteins referred to in this work as rPox1 and rPox2 exhibited comparable physicochemical properties including apparent molecular weights. In the case of human 80S ribosome, the protein present in the major labeled tRNA- rPox1 covalent complex was identified as the 60S ribosomal protein L36a-like (RPL36AL) by mass spectrometry. The molecular weight of the minor labeled tRNA-rPox2 covalent complex was estimated from the data of the 1-D SDS-PAGE, and a deduced molecular weight of 34,000 + 2,000 Da for the ribosomal protein referred to as rPox2 designated protein RPL5 as the candidate minor labeled protein of human 80S ribosome. Search for candidate ribosomal proteins for the tRNAox-labeled proteins rPox1 and rPox2 of 70S ribosome from E. coli designated RPL2 (M.W. 29,860 Da), the largest eubacterial rP as the tRNAox-labeled protein corresponding to the minor labeled human RPL5, and RPL15 (M.W. 14,980 Da) or RPL16 (M.W. 15,281 Da) as corresponding to the major labeled human RPL36AL.