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Project 1 – Designing a Reconstituted
Translation System.
The goal of this project is to design a reconstituted
translation system that can efficiently polymerize N-methyl
and cyclic amino acids in an mRNA display format.
Project 2 – Targeting the Serine Protease
Thrombin.
The goal of this project is to target the serine protease
thrombin with an mRNA display library containing one or
more N-methyl and cyclic amino acids for the purpose of
identifying ligands that are resistant to enzymatic degradation
as a prototype for broad drug lead discovery.
Project 3 – Building Unnatural Amino Acids
into the Translation Apparatus.
The goal of this project is to expand the chemical repertoire
used in protein synthesis at one of the functionally important
steps in translation, Elongation Factor-Tu recognition
of aminoacyl-tRNAs.
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Frankel,
A., S.W. Millward and R.W. Roberts. 2003. Encodamers:
Unnatural Peptide Oligomers Encoded in RNA. Chemistry
and Biology, 10:1043-1050.
Xia,
T., A. Frankel, J. Ren, T.T. Takahashi, and R.W. Roberts.
2003. The conformation of the nascent boxB mRNA/N protein
complex dictates the function of the phage antitermination
switch. Nature Structural Biology, 10:812-819.
Frankel,
A., S. Li, S.R. Starck, and R.W. Roberts. 2003. Unnatural
RNA display libraries. Current Opinion in Structural
Biology, 13:506-512.
Frankel,
A. and R.W. Roberts. 2003. In Vitro Selection for Sense
Codon Suppression. RNA, 9:780-786.
Frankel,
A., N. Yadav, J. Lee, S. Clarke, T.L. Branscombe, and
M.T. Bedford. 2002. The Novel Human Protein Arginine
N-Methyltransferase PRMT6 Is a Nuclear Enzyme Displaying
Unique Substrate Specificity. Journal of Biological
Chemistry, 277:3537-3543.
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