TY - JOUR
T1 - Natural amino acids do not require their native tRNAs for efficient selection by the ribosome
AU - Effraim, Philip R.
AU - Wang, Jiangning
AU - Englander, Michael T.
AU - Avins, Josh
AU - Leyh, Thomas S.
AU - Gonzalez, Ruben L.
AU - Cornish, Virginia W.
N1 - Funding Information:
This work was supported in part by funds to V.W.C. and R.L.G. Jr. from Columbia University and by grants to R.L.G. Jr. from the Burroughs Wellcome Fund (CABS 1004856) and T.S.L. from the US National Institutes of Health (RO1 GM54469). P.R.E. was supported by Columbia University College of Physicians and Surgeons’ MD/PhD Program (US National Institutes of Health Institutional Training Grant T32 GM07367). We thank Y.-M. Hou and M. Dupasquier (both at Thomas Jefferson University) for the kind gift of a nucleotidyl transferase overexpression strain, D. Tirrell (California Institute of Technology) for the gift of a phenylalanyl-tRNA synthetase overexpressing strain and N. Prywes (Columbia University) for cloning and purifying alanyl-tRNA synthetase as well as aiding in tRNAAla purification. We also thank H. Suga, R. Green, H. Zaher and L.G. Dickson for helpful discussions and advice. Finally, we are indebted to V. Mondol and S. Das for managing the Cornish and Gonzalez laboratories, respectively.
PY - 2009/12
Y1 - 2009/12
N2 - The involvement of tRNA structural elements beyond the anticodon in aminoacyl-tRNA (aa-tRNA) selection by the ribosome has revealed that substrate recognition is considerably more complex than originally envisioned in the adaptor hypothesis. By combining recent breakthroughs in aa-tRNA synthesis and mechanistic and structural studies of protein synthesis, we have investigated whether aa-tRNA recognition further extends to the amino acid, which would explain various translation disorders exhibited by misacylated tRNAs. Contrary to expectation, we find that natural amino acids misacylated onto natural but non-native tRNAs are selected with efficiencies very similar to those of their correctly acylated counterparts. Despite this, small but reproducible differences in selection indeed demonstrate that the translational machinery is sensitive to the amino acidg-tRNA pairing. These results suggest either that the ribosome is an exquisite sensor of natural versus unnatural amino acidg-tRNA pairings and/or that aa-tRNA selection is not the primary step governing the amino acid specificity of the ribosome.
AB - The involvement of tRNA structural elements beyond the anticodon in aminoacyl-tRNA (aa-tRNA) selection by the ribosome has revealed that substrate recognition is considerably more complex than originally envisioned in the adaptor hypothesis. By combining recent breakthroughs in aa-tRNA synthesis and mechanistic and structural studies of protein synthesis, we have investigated whether aa-tRNA recognition further extends to the amino acid, which would explain various translation disorders exhibited by misacylated tRNAs. Contrary to expectation, we find that natural amino acids misacylated onto natural but non-native tRNAs are selected with efficiencies very similar to those of their correctly acylated counterparts. Despite this, small but reproducible differences in selection indeed demonstrate that the translational machinery is sensitive to the amino acidg-tRNA pairing. These results suggest either that the ribosome is an exquisite sensor of natural versus unnatural amino acidg-tRNA pairings and/or that aa-tRNA selection is not the primary step governing the amino acid specificity of the ribosome.
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U2 - 10.1038/nchembio.255
DO - 10.1038/nchembio.255
M3 - Article
C2 - 19915542
AN - SCOPUS:73549106134
SN - 1552-4450
VL - 5
SP - 947
EP - 953
JO - Nature Chemical Biology
JF - Nature Chemical Biology
IS - 12
ER -