3-nitroTyr-RS8/tRNA(CUA)

RS/tRNA Foundational Publication Support

Neumann, Heinz, Jennifer L Hazen, John Weinstein, Ryan A Mehl, and Jason W Chin. (2008) 2008. “Genetically Encoding Protein Oxidative Damage.”. Journal Of The American Chemical Society 130 (12): 4028-33. doi:10.1021/ja710100d.

RS/tRNA Pair Development Year
2008

ncAA(s) Incorporated

3-nitro-L-tyrosine

ncAA Structure (png, jpg, jpeg)
3-Nitro-L-tyrosine
ncAA Utility
3-nitroTyr is a natural post-translational modification of proteins typically resulting from protein oxidation by peroxynitrite. It increases in many diseases and with age. Still unknown is if it can be reversed (by a denitrase) and if it has has a purposeful signaling role, or if it is only a modification associated with pathologies. It is known in some cases to contribute to disease pathology, but in most cases it is unknown how much it causes pathology vs. being a consequence of pathology. The ability to site specifically and quantitatively place 3-nitroTyr in positions in proteins that have been seen to occur in association with disease is a key tool to answer questions about its possible roles in normal physiology and disease.


RS Organism of Origin
Parent RS
RS Mutations
Y32R
H70L
Q155M
D158G
I159L
L162H

tRNA Organism of Origin
Parent tRNA
tRNA Anticodon
CUA
Other tRNA Mutations
C17A
U17aG
U20C
G37A
U47G

RS/tRNA Availability
n/a
Used in what cell line?

RS/tRNA Additional Notes
Yielded high fidelity incorporation into Mn superoxide dismutatase, but was later found inadequate for other proteins. Has been superseded by the third generation Mj 3NY-A7 RS/tRNA pair for work in E. coli.