? Accurate translation of the genetic code into functional polypeptides relies on critical events in molecular recognition. The aminoacyl-tRNA synthetases (AARSs) are at the heart of this process. These enzymes catalyze specific tRNA aminoacylation reactions. Their products, the aminoacyl-tRNAs, convert the nucleic acid genetic code into proteins within the ribosome. With only a few exceptions, each of the AARSs is exquisitely specific for a single cognate amino acid and a single class of tRNA isoacceptors. Glutamyl-tRNA synthetase (GluRS) is an unusual exception to this specificity rule; some GluRSs aminoacylate both tRNA(Glu), the cognate substrate, and the """"""""non-cognate"""""""" tRNA(Gln); in these cases, GluRS is termed non-discriminating (GluRS-ND). The pathogenic bacterium Helicobacter pylori relies on two GluRSs - a discriminating GluRS-D (GluRS1) and a second GluRS (GluRS2) that is neither discriminating nor non-discriminating. This Hp GluRS2 misacylates tRNA(GIn) with glutamate but does not readily aminoacylate """"""""cognate"""""""" tRNA(Glu). It is proposed that these two GluRSs represent intermediates in the evolution of a modern GluRS-D and a possible future, bacterial glutaminyl-tRNA synthetase (GInRS). Thus, GIuRS1 and GluRS2 can be used to experimentally probe the evolution of substrate specificity. The research described in this proposal will define the molecular differences that result in the fine-tuned tRNA specificities of these two enzymes, while concomitantly delineating the differences between GluRS-NDs and GluRS-Ds. Additionally, experiments will directly probe the amino acid specificity of GluRS2 to determine how this enzyme selects glutamate over glutamine, asking whether or not it can be converted into a functional, bacterial GInRS. In total, this proposal will provide detailed molecular insight into the subtle differences between the substrate specificities of closely related AARSs, while providing direct insight into how the evolution of these enzymes might have proceeded. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM071480-01A1S1
Application #
7084126
Study Section
Molecular Genetics C Study Section (MGC)
Program Officer
Lograsso, Philip
Project Start
2005-03-01
Project End
2010-02-28
Budget Start
2005-05-01
Budget End
2006-02-28
Support Year
1
Fiscal Year
2005
Total Cost
$14,724
Indirect Cost
Name
Johns Hopkins University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Silva, Gayathri N; Fatma, Shirin; Floyd, Ashley M et al. (2013) A tRNA-independent mechanism for transamidosome assembly promotes aminoacyl-tRNA transamidation. J Biol Chem 288:3816-22
Fischer, Frederic; Huot, Jonathan L; Lorber, Bernard et al. (2012) The asparagine-transamidosome from Helicobacter pylori: a dual-kinetic mode in non-discriminating aspartyl-tRNA synthetase safeguards the genetic code. Nucleic Acids Res 40:4965-76
Zhao, Liangjun; Dewage, Sajeewa W; Bell, Michael J et al. (2012) The kinase activity of the Helicobacter pylori Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase is sensitive to distal mutations in its putative ammonia tunnel. Biochemistry 51:273-85
Huot, Jonathan L; Fischer, Frederic; Corbeil, Jacques et al. (2011) Gln-tRNAGln synthesis in a dynamic transamidosome from Helicobacter pylori, where GluRS2 hydrolyzes excess Glu-tRNAGln. Nucleic Acids Res 39:9306-15
Chang, Keng-Ming; Hendrickson, Tamara L (2009) Recognition of tRNAGln by Helicobacter pylori GluRS2--a tRNAGln-specific glutamyl-tRNA synthetase. Nucleic Acids Res 37:6942-9
Cathopoulis, Terry J T; Chuawong, Pitak; Hendrickson, Tamara L (2008) Conserved discrimination against misacylated tRNAs by two mesophilic elongation factor Tu orthologs. Biochemistry 47:7610-6
Hendrickson, Tamara L (2008) Proofreading optimizes iodotyrosine insertion into the genetic code. Proc Natl Acad Sci U S A 105:13699-700
Cathopoulis, Terry J T; Chuawong, Pitak; Hendrickson, Tamara L (2007) A thin-layer electrophoretic assay for Asp-tRNAAsn/Glu-tRNAGln amidotransferase. Anal Biochem 360:151-3
Stanley, Ann Marie; Chuawong, Pitak; Hendrickson, Tamara L et al. (2006) Energetics of outer membrane phospholipase A (OMPLA) dimerization. J Mol Biol 358:120-31
Chuawong, Pitak; Hendrickson, Tamara L (2006) The nondiscriminating aspartyl-tRNA synthetase from Helicobacter pylori: anticodon-binding domain mutations that impact tRNA specificity and heterologous toxicity. Biochemistry 45:8079-87