In all cells, proteins are synthesized by ribosomes, megadalton RNA-protein machines that use aminoacyl-tRNA (aa-tRNA) substrates to translate messenger RNA (mRNA). In recent years, tremendous progress has been made in elucidating the structure of the ribosome in the absence and presence of substrates and various translation factors. Despite this wealth of structural information, several important questions about translation elongation and the role of rRNA in this process remain open.
Aim 1 of this proposal is to determine the role of 16S rRNA in decoding. A number of mutations in 16S rRNA that increase misreading in vivo will be characterized in vitro. The data obtained may reveal how signaling between the 30S A site and elongation factor EF-Tu is mediated.
Aim 2 of this proposal is to determine the molecular basis of ribosomal "unlocking," which limits the rate of translocation. Nine inter-subunit bridge mutations and four 30S neck mutations will be thoroughly characterized with respect to factor-independent and factor-dependent translocation in vitro. The data obtained will identify those ribosome- ribosome contacts contributing to the energy barrier for translocation and may help uncover the molecular basis of unlocking. Ribosomes are a main target of antibiotics, and defects in translation are associated with a growing number of inherited human diseases and cancers. Insight gained by this project may lead to the development of novel antimicrobial drugs and/or treatments for one or more hereditary diseases.
One of the largest challenges facing modern medicine is the emergence of antibiotic resistance, and many classes of medically useful antibiotics target the ribosome. Defects in protein synthesis have been attributed to many inherited human diseases, and a growing body of evidence suggests that alteration in ribosome biogenesis and/or activity plays an important role in the development of several cancers. Insight gained from this project may (1) aid efforts to develop novel antibiotics and/or therapy regimes to combat pathogens with multiple-drug resistance and (2) contribute to the treatment and/or prevention of one or more hereditary diseases and/or cancers.
|Ying, Lanqing; Fredrick, Kurt (2016) Epistasis analysis of 16S rRNA ram mutations helps define the conformational dynamics of the ribosome that influence decoding. RNA 22:499-505|
|Fleming, Ian M C; Paris, ZdenÄ›k; Gaston, Kirk W et al. (2016) A tRNA methyltransferase paralog is important for ribosome stability and cell division in Trypanosoma brucei. Sci Rep 6:21438|
|Liu, Qi; Fredrick, Kurt (2016) Intersubunit Bridges of the Bacterial Ribosome. J Mol Biol 428:2146-64|
|Fredrick, Kurt (2015) Another look at mutations in ribosomal protein S4 lends strong support to the domain closure model. J Bacteriol 197:1014-6|
|Fosso, Marina Y; Zhu, Hongkun; Green, Keith D et al. (2015) Tobramycin Variants with Enhanced Ribosome-Targeting Activity. Chembiochem 16:1565-70|
|McClory, Sean P; Devaraj, Aishwarya; Fredrick, Kurt (2014) Distinct functional classes of ram mutations in 16S rRNA. RNA 20:496-504|
|Xia, Xin; Piao, Xijun; Fredrick, Kurt et al. (2014) Bifacial PNA complexation inhibits enzymatic access to DNA and RNA. Chembiochem 15:31-6|
|Fredrick, Kurt; Ibba, Michael (2014) The ABCs of the ribosome. Nat Struct Mol Biol 21:115-6|
|Balakrishnan, Rohan; Oman, Kenji; Shoji, Shinichiro et al. (2014) The conserved GTPase LepA contributes mainly to translation initiation in Escherichia coli. Nucleic Acids Res 42:13370-83|
|Liu, Qi; Fredrick, Kurt (2013) Contribution of intersubunit bridges to the energy barrier of ribosomal translocation. Nucleic Acids Res 41:565-74|
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