Ribozyme with tRNA synthetase activity and methods of manufacturing and using the same
Ribozymes exhibiting tRNA synthetase activity and substrate specificity, as well as methods for engineering and producing the same, are disclosed. The ribozymes of the present disclosure comprise a T-box RNA module fused with a flexizyme module. The flexizyme module provides high promiscuity with respect to amino acid substrates and the T-box module provides tRNA substrate specificity. Systems are also described for aminoacylation of suppressor tRNAs with unnatural amino acids (uAAs), such systems comprising the ribozyme previously mentioned, suppressor tRNA, and the desired uAAs. Methods for incorporating a uAA into a growing polypeptide chain using the ribozyme hereof are also provided.
1. An artificial ribozyme comprising:
a T-box element comprising a 3′-terminus and a riboswitch element having a specifier loop for binding a cognate tRNA substrate with specificity; and
a flexizyme comprising SEQ ID NO: 2, which defines at least an active site for binding an unnatural amino acid, an acceptor end for base pairing to a terminus of a tRNA substrate, a nucleotide linker, and a P1 stem linked to the 3′-terminus of the T-box element,
wherein when the T-box element recognizes and preferentially binds the cognate tRNA substrate, the flexizyme can bind and aminoacylate the cognate tRNA substrate bound by the T-box element, and the active site of the flexizyme is not specific to a targeted unnatural amino acid.
2. The artificial ribozyme of claim 1 , wherein the T-box element comprises a bacterial T-box element derived from a Geobacillus kaustophilus and the flexizyme comprises a dinitro-flexizyme.
3. The artificial ribozyme of claim 1 , wherein the 3′-terminus of the T-box element and a 5′-terminus of the flexizyme are connected via a poly-A linker comprising between five and ten nucleotides.
4. The artificial ribozyme of claim 3 , comprising SEQ ID NO: 1.
5. The artificial ribozyme of claim 1 , wherein a 5′-terminus of the T-box element further comprises a guanine-adenine-guanine nucleotide sequence linked thereto to facilitate in vitro transcription of the artificial ribozyme.