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Regions of the M. jannaschii tyrosyl tRNACUA thought to interact with elongation factor Tu were randomized, and the resulting tRNA libraries were subjected to in vitro evolution. The tRNAs identified resulted in significantly improved unnatural amino acid-containing protein yields. In some cases, the degree of improvement varied in an amino acid-dependent manner.
tRNAs have evolved to act as highly efficient amino acid carriers and activators during each stage of protein synthesis. Each tRNA must be selectively charged by its cognate aminoacyl-tRNA synthetase (aaRS); the resulting aminoacyl-tRNA must be efficiently bound by elongation factor Tu (EF-Tu) for transport to the ribosome; after binding to the ribosomal A site, the aminoacyl-tRNA must function efficiently in translation as a substrate for the peptidyl transferase; and finally the tRNA bearing the growing peptide chain must be translocated to the P site, undergo another acyl transfer reaction, and be released from the ribosome. We and others have used orthogonal tRNA/aaRS pairs for the site-specific incorporation of nearly 50 unnatural amino acids in E. coli, S. cerevisiae, and mammalian cells in response to unique nonsense and frameshift codons.1 An engineered M. jannaschii amber suppressor tyrosyl-tRNA/tRNA-synthetase ( /MjYRS) pair has been the most extensively used system for the evolution of aaRS variants that incorporate unnatural amino acids in E. coli. Although unnatural amino acids are typically incorporated into proteins with good efficiency and excellent fidelity, further system optimization resulting in increased protein yields is highly desirable.
Because is derived from an archaeal tRNA and therefore significantly differs in sequence from E. coli tRNAs, it may not function optimally with the E. coli translational machinery. Furthermore, in vitro binding studies have shown that while correctly acylated tRNAs bind EF-Tu with near uniform affinity, tRNAs bearing non-cognate amino acids show a broad range of affinities for EF-Tu2, indicating that the tRNA body and the esterified amino acid make compensatory contributions to EF-Tu binding. A number of genetic, biochemical, and structural studies have implicated specific residues within the tRNA acceptor stem and T stem as being important for EF-Tu binding.3 tRNA misacylation has also recently been shown to perturb binding to the ribosomal A site.4 Therefore it is likely that tRNAs acylated with noncognate unnatural amino acids adversely impact the efficiency of protein synthesis due to non-optimal interactions with EF-Tu and/or the ribosome.
We have used in vitro evolution to optimize the sequence of with MjYRS and a panel of six evolved unnatural amino acid incorporating MjYRS variants, and have identified several unique tRNA sequences that confer significantly improved mutant protein expression in E. coli. While most tRNAs identified show some improvement in protein yields for all aaRSs tested, the degree of improvement for each tRNA often varies depending on the identity of the esterified amino acid.
Examination of the X-ray crystal structure of the T. aquaticus EF-Tu•E. coli cysteinyl-tRNACys•GDPNP ternary complex6 reveals that residues 1–3, 50–54, 63–67, and 73–76, which reside in the acceptor stem and T stem of the tRNA, are in close proximity to EF-Tu (Figure 1). Interactions with EF-Tu almost exclusively involve the tRNA backbone, although contacts also exist between EF-Tu and the base of residue 63. Based on the notion that mutation of the corresponding positions in might modulate its binding affinity for EF-Tu, we created a tRNA library (Library I, theoretical diversity 1.05 × 106, >99% coverage) in which the five base pairs of the T-stem (49–53, 61–65) were randomized. The tRNA library was subjected to a negative selection to remove tRNAs that are substrates for endogenous aaRSs using an amber mutant of the barnase gene as previously described5; positive selection of surviving clones to identify functional tRNA sequences was carried out in the presence of aaRS specific for tyrosine (1) (MjYRS), L-3-(2)-naphthlyalanine (2) (NapRS7a), p-azidophenylalanine (3) (pAzPheRS7b), p-iodophenylalanine (4) (pIPheRS7c), p-acetylphenylalanine (5) (pAcPheRS7d), and p-benzoylphenylalanine (6) (pBpaRS7e) (Scheme 1), chloramphenicol, and an amber mutant of chloramphenicol acetyltransferase (CAT) as previously described. The surviving tRNAs were then screened based on cell fluorescence using an amber suppressible GFPuv construct to identify the most active tRNAs (see supplementary material for experimental details). Nine unique tRNA sequences were identified with significantly improved protein yields compared to (supplementary Table S3). The G52-C62 and G53-C61 pairs, which are highly conserved among E. coli tRNAs, were invariant in all hits. The consensus sequence for the most active hits is W49NRGG53-C61CYNW65 (where W is A or T; N is A, T, G, or C; R is A or G; and Y is C or T).
Next, we constructed a second tRNA library (Library II, theoretical diversity 1.7 × 107, >99% coverage) in which the consensus sequences at positions 49–53 and 61–65 from the best Lib I hits were retained and the remaining positions in contact with EF-Tu (2, 3, 6, 7, 66, 67, 70, and 71) were randomized. Positions 1 and 72–76 were not mutated because of their high degree of conservation and their importance in recognition by MjYRS. Library II was subjected to the same selection/screening procedure as was used for Library I. In addition to the 6 previously used aaRSs, the aaRS specific for p-hydroxy-L-phenyllactic acid (7) (PlaRS)1c, was also used for positive selection. Fourteen unique tRNA sequences were identified that lead to significant improvements in protein yields compared to (supplementary Table S4). Of these, ten unique sequences were found to rank in the top 3 in terms of fluorescence intensity for at least one aaRS, and resulted in mutant protein yields 200–2200% of those obtained with (Table 1). Yield improvements were far greater with 6 (18 to 21-fold better than ) than with the other amino acids (100–350% better than ). Several of the best hits contained base deletions in the D-loop which arose as artifacts of library construction.
These 10 tRNAs were isolated, crossed against 13 aaRSs (the 7 used in this study and 6 additional aaRSs previously evolved for incorporation of bipyridylalanine (8) (Bpy)8a, hydroxyquinolinylalanine (9) (HQ)8b, sulfotyrosine (10) (SfY)8c, p-azobenzylphenylalanine (11) (pABPhe)8d, o-nitrobenzyltyrosine (12) (ONBY)8e, and 7-hydroxycoumarinylethylglycine (13) (Cou)8f) (Scheme 1) and assayed for GFP production in order to identify the tRNA sequence that confers the largest improvement in expressed protein yield for each amino acid. Improvements in yield of 175%–320% were seen with the best tRNAs charged with compounds 1–5, 8, 10, and 11. However, significantly larger improvements were observed with 9 (405%), 7 (420%), 13 (790%), 12 (2070%), and 6 (2520%) (Figure 2). Interestingly, the compounds with the most dramatic improvements in yield have bulky side chains. Notable exceptions include 7, which differs from tyrosine only by the replacement of the α-amino group with an α-hydroxyl group; and 11, which gave only a 255% improvement, yet has a bulky side chain. This data suggests that the structure of the unnatural amino acid can affect the ability of the corresponding aminoacyl-tRNA to function productively in translation. This may be a result of interactions between the amino acid and the EF-Tu binding pocket. Consistent with this hypothesis, it was recently shown that mutation of the EF-Tu amino acid binding pocket resulted in more efficient binding of tRNAs bearing bulky unnatural amino acids.9 The 195% yield increase observed with the natural amino acid 1 represents the baseline improvement of due to optimization of this archaeal tRNA for the E. coli translational machinery. Five tRNAs (Tyr1, pAzPhe1, Nap1, Nap3, and pIPhe1) consistently give the largest increases in yield. Of these, Nap1 is the best “general” hit (the tRNA that gives the best overall yield improvements with all amino acids). Yields of purified GFP expressed using Nap1 and a GFPN149TAG construct with 1–7 range from 2.7–16.3 mg/L (380–1175% of yields obtained with ) in rich media (supplementary Figure S9). The fidelity of unnatural amino acid incorporation with Nap1 and 1–7 was determined by LC-ESI-MS of purified GFP proteins produced using evolved tRNAs and is comparable to the high fidelity obtained with (supplementary Table S2, Figures S11–S17).
Growth rates were determined for E. coli TOP10 cells expressing the evolved tRNAs (with GFP N149TAG reporter, aaRS, IPTG, and 1–7) (supplementary Figure S10, Table S1). In all cell lines except those expressing PlaRS, the exponential growth rates for cells expressing the evolved tRNAs were significantly faster (μ= 0.47 ± 0.05 h−1) than for those expressing (μ = 0.30 ± 0.05 h−1), indicating that the evolved tRNAs are in general less toxic than . Because all tRNAs were subjected to negative selection to remove those that are substrates for endogenous aaRSs, it is unlikely that altered toxicity results from differences in orthogonality of the tRNAs. The decreased toxicity of the evolved tRNAs could result from decreased readthrough of natural stop codons, or altered interactions of the tRNA with EF-Tu and/or the ribosome which result in enhanced translation of heterologously expressed amber mutant genes. Several examples of suppressor tRNA-dependent cellular toxicity, in which toxicity was suggested to be the result of readthrough of endogenous stop codons, have been reported.10 The fact that cells expressing all evolved tRNAs charged with 1–6 have nearly the same growth rates yet display a broad range of protein yields, suggests that other factors in addition to ameliorated toxicity contribute to the improvements in protein yield.
A recent study on the EF-Tu binding affinities of a collection of acceptor stem and T stem mutations allows prediction of EF-Tu interaction strength based on sequence.3a This model predicts that our evolved tRNAs bind EF-Tu 0.3–0.9 kcal/mol more tightly than . The 51–63 base pair, which was changed from a U-G pair in to a G-C pair in all evolved tRNAs, is predicted to strengthen the EF-Tu binding affinity by 1.0 kcal/mol. The gain in function observed for the evolved tRNAs may be due in large part to this mutation, although convergence to non-wild-type sequences at other positions suggests that these mutations may act to fine-tune tRNA affinity for EF-Tu. It is possible that the predicted increase in binding energy between EF-Tu and the evolved tRNAs compensates for weaker binding of unnatural amino acids in the EF-Tu binding pocket, and that this compensation is the reason for the large yield improvements observed with some amino acids. Detailed analysis of the interaction of the acylated tRNAs with EF-Tu will provide additional insights into the mechanistic basis for the improved activities of these tRNAs.
In conclusion, we have utilized an in vitro evolution approach to identify variants with significantly enhanced activity for the incorporation of unnatural amino acids into proteins, especially the photocrosslinking amino acid 6, which is widely used to map biomolecular interactions. We also found that the degree of yield improvement is in some cases unnatural amino acid-dependent. These tRNAs will facilitate the creation of an optimized and standardized system for the genetic incorporation of unnatural amino acids into proteins in E. coli.11
Materials and methods can be found in the supporting information
This work is supported by NIH grants R01 GM062159 (P.G.S.) and F32 GM080067 (C.E.M.), and the Skaggs Institute for Chemical Biology.
Supporting information for this article is available on the WWW under http://www.angewandte.org or from the author.