Corrigendum: Site Specific Genetic Incorporation of Azidophenylalanine in Schizosaccharomyces pombe

Scientific Reports 5: Article number: 17196; published online: 24 November 2015; updated: 22 February 2016 This Article contains errors in the Acknowledgements section: “We express our sincere gratitude to the WPH Proteomics Research Technology Platform for the contribution to the mass spectrometry analysis.

Scientific RepoRts | 5:17196 | DOI: 10.1038/srep17196 using methods of genetics, molecular biology, biochemistry, genomics, and high resolution imaging. To expand the repertoire of technologies that can be used in fission yeast to study protein function, we sought to develop experimental approaches to expand the fission yeast genetic code and thereby to facilitate genetic incorporation of unnatural amino acids at specified locations into fission yeast proteins.
In this study, we expanded the genetic code of S. pombe. We have engineered S. pombe cells with an orthogonal E. coli tyrosyl-tRNA synthetase (TyrRS)/E. coli tRNA Tyr pair, enabling site specific incorporation of natural and unnatural amino acids through amber codon suppression. We show that the cross-linking nitrene generating amino acid azido-phenylalanine (AzF) can be introduced into three different proteins in fission yeast. We also show the ability of glutathione S-transferase containing AzF at position 52 (the dimerization site) to generate covalently linked multimers upon UV exposure. Our studies introduce a new and powerful approach to study function of fission yeast proteins.

Results
Expression and functionality of the orthogonal pair in S. pombe. Incorporation of the unnatural amino acids at a specified location within a protein of interest is achieved by the availability of 3 elements: 1. a codon that does not encode any natural amino acid and can encode the unnatural amino acid when present in the mRNA. 2. a tRNA that base-pairs with this codon and 3. an aminoacyl-tRNA synthetase that charges the tRNA with the unnatural amino acid 9 . It is also important that the tRNA and the tRNA synthetase are orthogonal. The amber codon (UAG) has been developed as a sense codon for the incorporation of several unnatural amino acids into proteins in recent years. It has been established that the tRNA for tyrosine (tRNA Tyr ) from Escherichia coli or Bacillus sterothermophillus and the tyrosyl-tRNA synthetase (TyrRS) from E. coli function as an orthogonal pair in many eukaryotes 12,14 . Furthermore, mutant versions of E. coli/B. stearothermophillus (tRNA Tyr ) with mutations in the anti-codon loop that base-pair with amber codon and aaRS that can charge these tRNAs with tyrosine or UAAs have been generated 9 . We therefore chose to use this orthogonal tRNA Tyr and TyrRS pair for genetic code expansion studies in fission yeast.
To expand the genetic code of S. pombe, we first designed a system to express tRNAs. It is known that an S. pombe tRNA Ser is co-transcribed with tRNA Met 15,16 (Fig. 1A Construct 1). Previous work has also led to the identification of sup3-5 as an opal suppressing tRNA Ser , which is known to suppress the adenine auxotrophic mutant ade6-704 ( Fig. 1A Construct 2) 17,18 . We designed two DNA constructs in which the tRNA Met was replaced with tRNA Tyr from B. stearothermophillus (Fig. 1A Construct 3) or E. coli (Fig. 1A Construct 4). All DNA constructs described in Fig. 1A constructs 2, 3, and 4 also carried the marker gene his5, into which an amber codon had been inserted in place of the codon for Tyr at position 63. The three DNA constructs were introduced into an ade6-704 his5Δ strain also expressing E. coli TyrRS (Fig. 1B Strain 1) and selected for growth on medium lacking adenine. Transformants thus obtained were tested for their ability to grow on medium lacking histidine. We found that cells expressing B. sterothermophillus or E. coli tRNA Tyr , but not strains expressing S. pombe tRNA Met were capable of growth on medium lacking histidine (Fig. 1C). The suppression efficiency for the heterologous pair, B. stearothermophillus tRNA Tyr and E. coli TyrRS was significantly lower than the suppression by E. coli tRNA Tyr and E. coli TyrRS , unlike in mammalian cells in which B. stearothermophillus tRNA Tyr was better than E. coli tRNA Tyr in effecting suppression 12,19,20 . These observations established that the bacterial tRNA Tyr -TyrRS functioned as an orthogonal pair in fission yeast where they functioned as an amber suppressor. We chose to work with E. coli tRNA Tyr in the rest of the study.
To incorporate unnatural amino acids through the expanded genetic code, we employed the mutated E. coli TyrRS designated as E. coli AzFRS, capable of charging E. coli tRNA Tyr with unnatural amino acid azido-phenylalanine (AzF) 9,10 . In this experiment, the construct ( Fig. 1A Construct 4) carrying the marker for yeast transformation (sup3-5) and expressing E. coli tRNA Tyr carrying CUA in the anti-codon position was introduced into ade6-704 his5Δ fission yeast strains expressing either E. coli TyrRS (Fig. 1B  Strain 1) or E. coli AzFRS (Fig. 1B Strain 2). The construct also carried a his5 selectable marker into which a UAG stop codon was introduced. Note that all transformants grew on medium lacking adenine, suggesting the existence of plasmids in the strains (Fig. 1D). The suppression of the UAG codon in his5, and the resulting growth on the medium lacking histidine, was observed when cells expressed E. coli tRNA Tyr and E. coli TyrRS, but not in cells carrying the E. coli AzFRS and E. coli tRNA Tyr (Fig. 1D). Importantly, cells expressing E. coli AzFRS and E. coli tRNA Tyr were able to grow only on medium lacking histidine but supplemented with AzF, confirming that AzF was genetically incorporated in a mechanism in which the UAG stop codon was read by the translation machinery as a codon for AzF (Fig. 1D).
Optimization of suppression of E. coli tyrosine tRNA pair in fission yeast His5p. Effective application of unnatural amino acids to study proteins functions in fission yeast cells is often challenging due to inefficient non-sense suppression and unnatural amino acid incorporation. Since an increase in the expression of the desired mRNA using a strong promoter led to a more robust suppression in budding yeast, we tested if this effect could be recapitulated in fission yeast 21,22 . In this experiment, we designed one new construct in which the expression of the gene of interest is driven by the strong inducible nmt1-mini promoter (Singh et al., unpublished observations), which contains 400 bp of nmt1 promoter ( Fig. 2A Construct 3). The gene we tested was a his5 mutant with an amber codon in place of the codon for Tyr63. Both E. coli tRNA Tyr and targeted gene his5 are encoded on a pNO13 plasmid ( Fig. 2A). Spot assays showed that all transformants grew on medium lacking adenine ( Visualization of the suppression of E. coli tyrosine tRNA pair in vivo and in vitro. We next investigated the ability of tRNA Tyr , TyrRS and AzFRS to suppress amber codon mutations in mRNA encoding a synthetic peptide fused between myosin II light chain (Rlc1p) and GFP and in mRNA encoding Glutathione-S-Transferase (GST) in place of the codon for Gly at position 6 ( Fig. 3A).
To investigate suppression of amber stop codon in vivo, a DNA molecule in which one amber stop codon TAG was placed between rlc1 and GFP was introduced into an ade6-704 his5Δ strain expressing either TyrRS or AzFRS and GFP fluorescence was monitored. In the strain expressing TyrRS, GFP fluorescence in the actomyosin ring was observed in the presence or in the absence of AzF in the medium. However, in the strain expressing the AzFRS, GFP fluorescence was detected in the ring only when cells were grown on medium containing AzF (Fig. 3B). We ensured that the lack of rings in medium lacking AzF was not due to a defect in entry into mitosis (Fig. 3C), since the proportion of binucleate cells in the strain expressing TyrRS in the absence of AzF was not significantly different from the growth in the presence of AzF.
Next we checked suppression when a UAG codon was introduced into RNA encoding a third reporter protein Glutathione-S-Transferase, GST. Again, suppression was observed in the presence and absence of AzF when TyrRS was expressed. However, full length GST was not detected in the cells expressing AzFRS when cultured in the absence of AzF, but was present when cells were grown in the presence of AzF (Fig. 3D). Presently, we do not understand why the suppression is reduced in the presence of AzF when TyrRS and tRNA Tyr are used. It is possible that AzF and Tyr may compete for a similar binding site on TyrRS, which might affect the incorporation of Tyr in the presence of AzF, notwithstanding the fact that tRNA Tyr can only be charged with tyrosine. Collectively, our studies have shown efficient non-sense suppression within 3 mRNAs and also that the unnatural amino acid AzF can be introduced in a site-specific manner into fission yeast proteins.

Azido-phenylalanine incorporation in response to an amber stop codon. To further verify
site-specific incorporation of AzF into the protein of interest and to determine its occupancy at the amber position (position 6) rather than any other amino acid, the GST protein purified from cells expressing TyrRS, GST (G6Y), and from cells expressing AzFRS, GST (G6AzF), were analyzed by nano LC-ESI-MS/MS after digestion with trypsin. The GST peptide (SPILYYWK) that incorporates tyrosine at position 6, was readily identified by mass spectrometry from cells expressing TyrRS as a 2+ ion of 535.29 m/z (Fig. 4 top). Curiously, despite the AzF-dependent suppression of the UAG codon in GST protein upon expression of AzFRS, we were unable to detect the expected mass increase of 131 Da from the wild type GST peptide SPILGYWK (Supplemental Fig. 1A) that would represent incorporation of AzF. However, we identified a 2+ ion of 534.80 m/z that fragmented to match peptide SPILFYWK with the F modified by an additional 15 Da of mass. The position of the F + 15 Da modification is supported by y ions 4, 5, 6, 7 (Fig. 4 bottom). It is known that AzF can be reduced to p-amino-L-phenylalanine (AmF) during sample preparation 9,10,23 . We suggest that AzF at position 6 was reduced to AmF, which would be consistent with the molecular weight observed (Supplemental Fig. 1B). Taken together, we conclude that AzF is site specifically incorporated in response to an amber codon into S. pombe proteins and is readily converted into AmF.

Covalent cross-linking in GST upon incorporation of AzF.
Azido-phenylalanine is a nitrene generating cross-linking amino acid, whose reactive nitrenes can be generated by exposure of the protein with ultraviolet light. Although the bulk of AzF appeared to be converted to AmF, we reasoned that a  Table S1 for the strain number. T-indicates that cells were placed on agar plates lacking thiamine, which suppresses the nmt1 promoter.
Scientific RepoRts | 5:17196 | DOI: 10.1038/srep17196 fraction of AzF might still be present in the mixture and might be able to covalently cross-link with interacting proteins. To develop this system further, we generated GST with a UAG codon in place of the codon for Phe52, a site known to be involved in GST-dimerization 24 . UAG codon suppression was achieved upon expression of TyrRS and AzFRS, in which case suppression required the presence of AzF in the medium (Fig. 5A). Upon exposure to UV, GST carrying AzF at Phe52, but not GST carrying tyrosine at Phe52, was converted into covalently linked multimers that ran slower on SDS-PAGE (Fig. 5B). These experiments established that despite the conversion of the majority of AzF to AmF a fraction of GST may contain AzF which aids in UV cross-linking.

Discussion
In this study, we have developed the tools to introduce the unnatural amino acid AzF in a site-specific manner into Schizosaccharomyces pombe proteins. We have achieved this by the generation of S. pombe strains expressing orthogonal pairs of bacterial tRNA (that base pair with the UAG non-sense codon) and aminoacyl-tRNA synthetases (for natural or unnatural amino acids). Using this approach we have succeeded in introducing tyrosine and the nitrene-generating unnatural amino acid, azido-phenyl alanine  Table S1 for the strain number.
(AzF) into three proteins (GST, His5p, and a synthetic linker peptide). We did not observe any major deleterious phenotypic effects in cells carrying non-sense suppressor tRNA and aaRSs. Thus non-sense suppression based on introduction of unnatural amino acids can be used to study fission yeast protein structure and function. This work has also established that the E. coli and B. stearothemophilus tRNA Tyr and E. coli TyrRS function as an orthogonal pair in fission yeast.
Although non-sense suppression was only observed in the presence of all three factors, 1. tRNA Tyr , 2. AzFRS, and 3. AzF in the growth medium, we were unable to detect AzF in mass spectrometric analysis. Rather we found a peak consistent with conversion of AzF to amino-phenylalanine (as described in previous work) 9,10,23 . The conversion of AzF to AmF reduced the utility of the current system we have developed. Additional work is required to prevent reduction of AzF to AmF, so that the system can be used in protein-protein interaction studies. We have detected covalent cross-links between GST   Table S1 for the strain number. (B) The purified GST was exposed to UV light at 254 nm for 5 min and western blot with GST antibodies.
Scientific RepoRts | 5:17196 | DOI: 10.1038/srep17196 molecules, suggesting that despite our inability to detect an AzF peak in mass spectrometry, a fraction of GST should contain unreduced bona fide AzF.
In western blot analysis, we found that the amount of GST was less in non-sense suppressed strains compared to the level of GST expressed from mRNA that did not have an internal non-sense codon (data not shown). This is consistent with previous work that non-sense suppression is an inefficient process 12 . In addition, non-sense mediated decay of mRNA might also affect transcript abundance, as has been shown in C. elegans and S. cerevisiae 11,25 . Consistently, an increase in non-sense suppression was observed in S. cerevisiae, strains defective in the NMD pathway 26 . Development of such strains should increase the non-suppression efficiency in fission yeast.
Site-specific incorporation of AzF has been achieved in the budding yeasts S. cerevisiae and C. albicans. However, the biology of S. pombe allows for the investigation of a number of cell biological questions (such as cytokinesis and RNA interference) that are not easily tackled in budding yeasts. Our work on incorporation of site-specific incorporation of AzF, thus fills an important gap and opens up a new avenue to study fission yeast protein function. Further refinement of this method is necessary to allow full utilization of this approach to investigate protein function.

Methods
Media and growth conditions. Cells were grown and maintained in the yeast extract medium (YES) or Edinburgh minimal medium with appropriate supplements, as described in Moreno et al. (1991) 27 . YPD medium containing 1% yeast extract (Gibco-BRL), 2% peptone (Gibco-BRL) and 2% glucose was mainly used for mating and sporulation. All experiments were done at 30 °C which is the optimal growth temperature for tRNA Tyr -TyrRS expressing fission yeast strains, unless indicated otherwise. To suppress the stop codon in rlc1-TAG-gfp which was expressed under nmt1 promoter control, cells were grown in thiamine containing medium (repressing condition) overnight, followed by three washes with medium lacking thiamine and growth for another 6 h in medium lacking thiamine but supplemented with unnatural amino acid before imaging.
Plasmid construction. All the polymerase chain reactions are performed on a T100 Thermal Cycler from BIO-RAD. Inverse PCR based plasmid construction method was used to generate tRNA Tyr expression constructs as well as mutations on the gst and rlc1-gfp. For inverse PCR, two primers were designed to introduce insertion fragment. Each primer was ~50 bp in length and contained ~25 bp overlap with the plasmid backbone sequence. A standard PCR was performed firstly to generate the insertion fragment. 500 ng of the purified PCR product was used as primer in a 50 μ L inverse PCR mixture which contained 30 ng of plasmid template, 5 μ L of dNTP, 5 μ L of Pfu buffer, 1 μ L Pfu and ddH 2 O made up to 50 μ L. For site-directed mutagenic PCR, most steps were the same as in the inverse PCR. The only difference was the targeted mutation was designed into the primers and located into the middle of the overlap region of forward primer and reverse primers.

S. pombe Lithium Acetate transformation.
To transform plasmids into fission yeast cell, 20 mL overnight culture (a concentration of 0.5-1 × 10 7 cells/ml (OD 595 ≈ 0.5)) was harvested at 3,000 rpm for 1 min and washed with 1 mL LiAc/TE buffer (made from 100 mM lithium acetate pH 7.5, 10 mM Tris-HCl and 1 mM EDTA pH 7.5). After suspending cells in 100 μ L LiAc/TE buffer, 2 μ L SSDNA (sonicated salmon sperm carrier DNA, Stratagene) and 2 μ g DNA fragments (linearized) or plasmids were added to the suspended cells and incubated at room temperature for 15 min. Next, 240 μ L of PEG/LiAc/ TE (40% w/v PEG 4000 in 100 mM LiAc, 10 mM Tris-HCl, 1 mM EDTA) was added to cells followed by gentle mixing. After incubating them at 30 °C for 45-60 min, 43 μ L of dimethyl sulfoxide (DMSO) was added to the cells followed by gentle shaking. Cells were heated at 42 °C for 5 min and rinsed with sterile water. Cells were resuspended in 100 μ L water and plated on the selective agar plates.
Western Blot. Cells were lysed by glass bead disruption and eluted with lysis buffer (50 mM Tris-HCl pH 7.4, 150 mM NaCl, 5 mM EDTA, 1 mM PMSF, supplemented with protease inhibitors (Complete EDTA-free; Roche Diagnostics, Basel, Switzerland)). The lysate was clarified by centrifugation at 200 g. The supernatant was heated at 100 °C for 5 minutes after the addition of 2× Laemmli sample buffer and dithiothreitol. For western blotting, equal volumes of each sample were loaded on SDS-polyacrylamide gels of appropriate concentration and run at a constant current of 20 mA for 80 min. Note that the maximum voltage was lower than 200 V. After SDS-PAGE, proteins were blotted to PVDF (Polyvinylidene fluoride) membranes at a constant voltage of 90 V for 100 min at 4 °C. Transfer buffer used was 25 mM Tris-HCl pH 8.3, 192 mM glycine, 10% v/v methanol. Membranes were incubated with appropriate concentration of primary antibodies in blocking buffer (5% w/v milk, 0.05% v/v Tween-20 in TBS or PBS) at room temperature for 3 h or 4 °C overnight. After washing the blots thrice with PBST or TBST with gentle agitation, secondary antibodies were added and incubated at room temperature for 1 h. Signals were detected using the ECL approach 28 .
Glutathione S-transferase purification. Cell extract preparation for the glutathione S-transferase purification was as described for the western blot experiments. The extracts were incubated for 1-2 h at 4 °C with 20 μ L of pre-swollen glutathione-sepharose 4B (GE healthcare) beads equilibrated with lysis buffer (150 mM NaCl, 50 mM Tris pH 8.0, 10% Glycerol, complete protease inhibitors and 1.5 μ g/mL of PMSF). The supernatants were removed after centrifugation at a speed of 1,000 rpm for 2 min. The beads were washed with PBS containing protease inhibitors twice and lysis buffer containing 0.1% Triton-X100 once. The final elution buffer was 50 mM Tris/HCl, 10 mM reduced Glutathione, pH 8.0. Two fractions were collected.
His-tag purification. Cell extracts from 300 mL cell for the His purification was prepared as described for the western blot experiments. The extracts were incubated for 1-2 h at 4 °C with 300 μ L of pre-washed HisPur Ni-NTA Resin (Thermo Scientific) equilibrated with lysis buffer (150 mM NaCl, 50 mM Tris-Cl pH 8.0, 10% glycerol, complete protease inhibitors and 1.5 μ g/mL of PMSF). The supernatants were removed after spinning down at a speed of 2,000 rpm for 2 min. The beads were washed with lysis buffer with 20 mM imidazole thrice. The final elution buffer was lysis buffer contained 500 mM imidazole.
GST UV Crosslinking. Purified GST proteins containing unnatural amino acid AzF or tyrosine were used in this experiment. The concentration of purified proteins was estimated and diluted to equivalent levels. 20 uL of each sample was loaded on parafilm, which was kept on an icebox. Samples were exposed to UV (254 nm) in UV crosslinker CL-1000 (VWR) for 5 min and collected into a microfuge tube.
Spinning Disk Microscopy. Spinning disk images were captured by Andor spinning disk. Andor spinning disk using a Nikon ECLIPSE Ti-E microscopy equipped with a Plan Apo Vc 100× /1.40 N.A. Oil objective lens, a Yokogawa CSU-X1 unit spinning disk system, Andor iXon Ultra EMCCD (16 um/pxl) camera with 2× adapter for CSU-X1 and Andor iQ3 software. 405, 488, 561 and 640 nm solid state diode (power 50/100 mW) laser were used for excitation. All images were processed and analyzed by using ImageJ (http://rsb.info.nih.gov/ij/) software. Graphs in this paper were made by Excel.