تفاعل #2307982

ord-5b4a92b49bfc450c86ce1f646535cd48

معادلة التفاعل

N[C@@H](Cc1ccc2ccccc2c1)C(=O)O
L-3-(2-naphthyl)-alanine
N[C@@H](Cc1ccc2ccccc2c1)C(=O)O
L-3-(2-naphthyl)-alanine
Nc1nc2c(c(=O)[nH]1)N=C(CNc1ccc(C(=O)N[C@@H](CCC(=O)[O-])C(=O)O)cc1)CN2
dihydrofolate
N[C@@H](Cc1ccc(O)cc1)C(=O)O
tyrosine

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىprotein purification

الإجراء التجريبي

An L-3-(2-naphthyl)-alanine mutant of mouse dihydrofolate reductase (DHFR) was generated and characterized to confirm the ability of the mtRNACUATyr/SS12-TyrRS pair to site-specifically incorporate L-3-(2-naphthyl)-alanine in response to an amber stop codon. The Tyr163 codon of the mouse DHFR gene was mutated to TAG, and a His6 tag was added to the COOH-terminus of DHFR to facilitate protein purification using Ni2+ affinity chromatography. As a positive control, wild-type M. jannaschii TyrRS was coexpressed with the mtRNACUATyr resulting in efficient suppression of the TAG codon with tyrosine (FIG. 4). When SS12-TyrRS was coexpressed with the mutRNACUATyr in the presence of 1 mM L-3-(2-naphthyl)-alanine, full-length mouse DHFR was also generated (with yield of 2.2 mg/L in liquid GMML minimal medium). In the absence of either L-3-(2-naphthyl)-alanine, mtRNACUATyr or SS 12-TyrRS, no full length DHFR was produced. A penta-His antibody was used to detect the His6 tag at the COOH-terminus of DHFR in a Western blot. No DHFR could be detected in the absence of each of the above three components.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07368275B2uspto-grants-2008_05