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We present a flexible, real-time-coupled transcription–translation assay that involves the continuous monitoring of fluorescent Emerald GFP formation. Along with numerical simulation of a reaction kinetics model, the assay permits quantitative estimation of the effects on full-length protein synthesis of various additions, subtractions or substitutions to the protein synthesis machinery. Since the assay uses continuous fluorescence monitoring, it is much simpler and more rapid than other assays of protein synthesis and is compatible with high-throughput formats. Straightforward alterations of the assay permit determination of (i) the fraction of ribosomes in a cell-free protein synthesis kit that is active in full-length protein synthesis and (ii) the relative activities in supporting protein synthesis of modified (e.g. mutated, fluorescent-labeled) exogenous components (ribosomes, amino acid-specific tRNAs) that replace the corresponding endogenous components. Ribosomes containing fluorescent-labeled L11 and tRNAs labeled with fluorophores in the D-loop retain substantial activity. In the latter case, the extent of activity loss correlates with a combination of steric bulk and hydrophobicity of the fluorophore.
Protein synthesis is being studied intensively with a variety of motivations, ranging from practical needs for the development of efficient methods of cell-free protein synthesis (CFPS) for production of proteins that are difficult to express in cells (1–3), for the identification of new antibiotics (4,5), and toward achieving understanding of basic mechanisms of individual steps of the translation cycle and of overall protein synthesis (6,7). Many mechanistic studies employ fluorescent-labeled constituents of the protein synthesis machinery. Fluorescent probes permit real-time monitoring of specific reaction steps (8–15), but raise the question of whether introduction of exogenous labels unduly affects the processes under study. Assays of protein synthesis in current use are often cumbersome, involving aliquot removal and subsequent point-by-point determinations of bioluminescence (3), fluorescence (16,17), gel densitometry (16), enzymatic activity assay (18,19) or incorporation of radioactive amino acids (20–22).
Here we present a flexible, real-time coupled transcription–translation assay that, along with numerical simulation of a reaction kinetics model, permits quantitative estimation of the effects on full-length protein synthesis of introducing fluorescent probes, or other modifications, into components of the translational machinery. The assay involves the continuous monitoring of the formation of Emerald GFP (EmGFP), a rapidly maturing variant of green fluorescent protein (23), using a suitable plasmid and a commercially available CFPS kit derived from Escherichia coli (24). Straightforward alterations of the assay permit determination of (i) the fraction of ribosomes in a cell-free protein synthesis kit that is active in full-length protein synthesis and (ii) the relative activities in supporting protein synthesis of modified (e.g. mutated, fluorescent-labeled) exogenous components (ribosomes, amino acid-specific tRNAs) that replace the corresponding endogenous components.
Since the assay uses continuous fluorescence monitoring, it is much simpler and more rapid to use than other assays of protein synthesis and is compatible with high-throughput formats. It should thus find widespread application in many studies measuring protein synthesis in vitro. However, the assay does have the significant limitation that it is extremely stringent, since it treats as fully inactive those ribosomes that produce only partial or otherwise non-fluorescent EmGFP polypeptides.
All solutions contained water of high purity generated by MilliQ deionizer equipped with pyrogen free filter (Biopak, Millipore) to ensure the absence of contaminating RNAses, DNAses and proteases. All ultracentrifugations at 110000r.p.m. were carried out in a S120AT2 rotor in a Sorvall M120SE ultracentrifuge. Ribosome concentrations were calculated assuming 26pmol/A260 (25).
The pREST-EmGFP plasmid (Invitrogen, Inc.) contains a reading frame that includes a 40-residue N-terminal His-tag sequence followed by the 239-residue EmGFP sequence. We used standard mutagenesis techniques to introduce two modifications. The first, following reference (26), was to add a 31-residue C-terminal segment ending with the HindIII restriction site that, following plasmid linearization with HindIII, resulted in a reading frame devoid of a stop codon. This allowed tethering of mature, nascent EmGFPs to the ribosomes. The second change was a point mutation (S4F) near the beginning of the N-terminal His-tag sequence that was introduced for use in other studies. Mutagenesis was performed using a QuikChange Lightning site-directed mutagenesis kit (Stratagene, Inc.) with primers set according to the manufacturer's instructions.
All preparative steps were carried out on ice or at 4°C. S30 fractions of E. coli strains MRE600 (wild type) and AM77 (−L11) were prepared as previously described (27) using a French Press at 5000psi. Crude ribosome pellets were prepared by centrifuging S30 fractions at 110000rpm for 12min at 4°C either directly (S100P), or by layering the S30 lysate on a sucrose cushion (S100sucP, using 1.1M sucrose in TAM15 buffer) followed by resuspending the resulting pellet in TAM15 buffer. Small scale ribosome purification (70S-ss) was achieved by layering S100sucP ribosomes on a linear 15–30% sucrose gradient and collecting the 70S peak as described, using a VTi50 rotor (28). Large-scale ribosome purification (70S-ls) was achieved by sucrose gradient centrifugation using a zonal rotor as described (9). S100P preparations of AM77L11or AM77L11Cy3 ribosomes were prepared by incubating AM77 S30 fractions with a 2-fold excess of either unlabeled C38S/S87C-L11 (L11) or Cy3-labeled C38S/S87C-L11 (L11Cy3) at 37°C for 15min prior to high-speed pelleting. The preparation of the L11 variant and its labeling by Cy3 is described in (11). FPLC-purified L11Cy3 contained 1.0 Cy3/protein.
The CFPS kit (RTS 100 E. coli HY kit – previously sold by Roche Applied Science, currently sold by 5prime) was utilized to synthesize EmGFP according to the manufacturer’s manual, with some modifications. The CFPS kit is made up of five vials, containing cell lysate (V1), reaction mixture (V2), 19 amino acids (V3), methionine (V4), reconstitution buffer (V5) and a control GFP vector that was substituted throughout these experiments with the modified pREST-EmGFP plasmid described above. In the standard reaction, the following components are pre-mixed on ice: 2.4μl V1, 2μl V2, 2.4μl V3, 0.2μl V4, 1μl V5 and 2μl (130ng) plasmid in water. The total reaction volume was ~10μl. Fluorescence is recorded continuously at 30°C. The V3 solution was sometimes substituted by a home-made solution that contained approximately twice the original amino acid concentrations (denoted V3a). V3a, made up in V5, contained 8.33mM tyrosine, 16.66mM of each of the 18 other amino acids and no methionine. Final amino acid concentrations in the CFPS mixture were: 10mM Met, 1mM Tyr and 2mM of the other amino acids. All other lyophilized CFPS components, were dissolved in V5 according to the manufacturer’s manual, flash-frozen and stored at −80°C in single-use aliquots.
To test the activity of various buffers (Figure 1A) the following components were mixed: 2.4μl V1, 2μl V2, 1.2μl V3a, 0.2μl V4, 9.2μl of the indicated buffer and 0.45μl plasmid (stock solution 430ng/μl in water). V3a was made up in the indicated buffer rather than in V5. The total volume of the reaction was ~15μl. This combination yielded a reaction mixture that contained at least 70% of the indicated test buffer by volume and 30% of V5 used to reconstitute the lyophilized V1, V2 and V4. The buffers tested, included: TAM15: 50mM Tris–HCl pH 7.5, 30mM NH4Cl, 70mM KCl, 15mM Mg(Ac)2, 1mM DTT; TAM7: 50mM Tris–HCl pH 7.5, 70mM NH4Cl, 30mM KCl, 7mM MgCl2, 1mM DTT (29); Polymix Buffer: 50mM Tris–HAc pH 7.5, 5mM NH4Ac,100mM KCl, 15mM Mg(Ac)2, 0.5mM Ca(Ac)2, 6mM 2-mercaptoethanol, 5mM putrescine and 1mM spermidine (30); Polyamine Buffer: 20mM HEPES–KOH pH 7.5, 150mM NH4Ac, 4.5mM MgAc2, 4mM 2-mercaptoethanol, 0.05mM spermine and 2mM spermidine (31).
Ribosomes were removed from a mixture containing 2.4μl V1, 2μl V2, 1.2μl V3 and 0.2μl V4 as the pellet formed by ultracentrifugation at 110,000rpm for 12min at 4°C to yield the CFPS-ribosome kit. EmGFP synthesis was accomplished by adding 2.2μl of 6.8μM stock solution of home-made ribosomes (see above) in TAM15 buffer to the kit and initiating reaction with 130ng of plasmid in 2μl water. The final ribosome concentration of 1.5μM equals the concentration found in the CFPS kit.
Construction of the CFPS-Phe kit required treatment of various solutions with an inhibition cocktail [100µl of a commercial mixture of protease inhibitors (Halt, Pierce) and 0.5µl of 4.7M N-benzyl-2-phenylethylamine (Acros), a Phe-RS inhibitor (32)] and preparation of a V3a solution lacking Phe (denoted V3a-Phe). Additional details are found in Supplementary Information 2C and Supplementary Figure S3C. In addition, the normal ribosome concentration was sometimes reduced by half.
V1 (24μl) was combined with 0.24μl of an inhibition cocktail and the resulting mixture was dialyzed against 40ml of TAM15 buffer supplemented with 5% PEG-8000 (Fisher) in 3.5kDa cutoff micro-dialysis cups (Slide-A-Lyzer, Pierce—soaked in water for 15min prior to first use). Following dialysis at 4°C for 30min, 0.24μl of fresh inhibition cocktail was added and dialysis was repeated against fresh buffer. The dialyzed V1 solution (24μl) was combined with 20μl V2, 12μl V3a–Phe, 2μl V4, 0.24μl inhibition cocktail and 0.42μl 10× of Polyamine buffer, generating the CFPS-Phe solution. Reduction of ribosome concentration was accomplished by combining equal volumes of a ribosome-containing CFPS-Phe kit and a ribosome-depleted CFPS-Phe kit, prepared via high-speed centrifugation as described above.
EmGFP synthesis was accomplished by adding aqueous solutions (3.8μl) of various concentrations of Phe-tRNAPhe or Phe to the CFPS-Phe kit (6.2µl), followed by incubating the resulting mixture at 37°C for 5min to promote ternary complex (EF-Tu·aa-tRNA·GTP) formation, and initiating the reaction with 130ng plasmid in water (0.3μl). Addition of EF-Tu in amounts equimolar with added Phe-tRNAPhe results in a loss of EmGFP production (Supplementary Information 2F and Supplementary Figure S3F).
Assays were performed at 30°C. Most assays were carried out in triplicates on a reaction volume of 10μl dispensed in 384 well-plates (Greiner Bio-One 784076). Readings were taken every 20–45s for 30–70min in a plate reader (Envision 2103, Perkin-Elmer). The exposure time for individual fluorescence determinations was ~30ms using 10 flashes/measurement. In the absence of dye-labeled exogenous components, filters/bandpass settings of λex=486/10nm, λem=535/25nm were employed. To overcome spectral overlap of EmGFP emission with Cy3 and/or Cy5, the optimal settings were found to be λex=450/8nm, λem=510/10nm (see Supplementary Information 3 and Supplementary Figure S5). Some assays were also carried out using a reaction volume of 15μl placed in a sub-micro fluorometer cell (Starna Cells, Inc) placed within a spectrofluorometer (Hobira Jobin Yvon) (λex=468nm, λem=510nm). Kinetic traces were recorded over 30min at 10s intervals, using a 1s integration time.
EmGFP displays a fast component of photobleaching (33). To minimize photobleaching, sample irradiation was avoided except during recording, both in the fluorometer and in the plate reader. In a control experiment, no appreciable loss in EmGFP fluorescence could be detected over 70min for purified EmGFP added to a CFPS-Phe kit using the employed plate reader configuration, although photobleaching was evident for EmGFP that was dissolved in TAM15 buffer.
Cell-free protein expression was performed for 1h at 30°C with 130ng circular or linearized plasmid DNA per 10μl reaction volume. Anti-tmRNA [SsrA (34)] at a final concentration of 5μM (6) was premixed with the reaction mixture, and reaction was initiated with linearized plasmid. The reaction mixtures were incubated either in the plate reader while following fluorescence in real time, or in a temperature controlled bath for one hour and subsequently pulled-down through a sucrose cushion. In pull-down assays, reaction volumes of 30μl were layered onto ice-cold 1.1M sucrose in TAM15 buffer (100μl) and centrifuged at 110000rpm for 40min at 4°C. The supernatant was collected and the pellet was suspended in 30μl TAM15 buffer. EmGFP in the supernatant and in the pellet were quantified in the plate reader using a fluorescence calibration curve (Supplementary Information 1 and Supplementary Figure S1). The calculated ratio of EmGFP per ribosome in the pellet represented the fraction of active ribosomes.
Samples were prepared with CFPS-Phe as described above, except the final sample volume was 15μl. The [14C]-Phe-tRNAPhe variants were used at final concentrations of 10μM. The reaction was initiated by plasmid addition and incubated at 30°C for 30min. The reaction was quenched by the addition of 0.3ml 5% TCA (ice-cold), heated to 95°C for 15min, cooled on ice, filtered through a nitrocellulose filter, and washed five times with 1ml of 5% ice-cold TCA. The filter was then dissolved in 1ml ethyl acetate. Precipitated radioactivity, accurate to ±8%, was determined above a background equal to the radioactivity obtained with a sample that did not contain the EmGFP plasmid.
Four parameters were evaluated from the fluorescence traces that contained various Phe-tRNAPhes, using Origin software (OriginLab Corporation). Estimates of lag time, tL, maximum synthesis rate, S1 and final protein synthesis rate, S2, were obtained from the time of the maximal value of the second derivative, the maximal value of the first derivative, and a linear fit of the last eleven time points, respectively. Amplitude of the rapid synthesis period, A1, was determined by the intercept of two linear regression lines, the first centered at the point of maximal slope and the second fitted as described for S2. Before taking derivatives, the traces were smoothed using a 5-point adjacent average. All linear fits were performed using 11 time points. All values were normalized to the data obtained for 2μM E. coli Phe-tRNAPhe.
A model of the kinetics of EmGFP fluorescence accumulation in the CFPS experiment was written in MATLAB version 7.5.0 (R2007b). Details of the algorithm are described in Supplementary Information. The MATLAB code is supplied as Supplementary File S2. A compiled executable file may also be obtained upon request to one of the corresponding authors.
We employed a construct containing the 239-residue EmGFP sequence in between a 40-residue N-terminal His-tag extension and a 31-residue C-terminal extension. The latter sequence permitted the native EmGFP polypeptide to leave the ribosomal exit tunnel, allowing folding and maturation of EmGFP while the peptide is still attached to the ribosome. Translation of EmGFP followed by fluorophore maturation results in an accumulation of fluorescence intensity, providing a readily detectable signal that, after an initial lag phase, increases continuously in real time, reaching a near plateau after 60–90min (Figure 1). Four different buffers were examined, with the amounts of fluorescent EmGFP formation falling in the order Polyamine (31) > TAM15 (11) > Polymix (30) TAM7 (29) (Figure 1A), with the Polyamine buffer showing similar activity to the buffer provided with the kit (unknown composition). Accordingly, only the Polyamine buffer [having a composition similar to that used previously to support transcriptional activity (35)] or the TAM15 buffer was used in subsequent translational activity assays. We also tested whether pre-transcribed mRNA would program ribosomes to produce EmGFP in the CFPS kit. Translation rates and amounts were comparable to the coupled transcription-translation beginning from the DNA plasmid (data not shown).
We next determined the fraction of active ribosomes present in a CFPS kit, as measured by the amount of ribosome-associated nascent EmGFP complex formed, adapting a known procedure (26). In this approach the EmGFP plasmid is linearized to remove the stop codon, preventing re-initiation on a new mRNA, and anti-tmRNA oligonucleotide complementary to the tmRNA sequence is added to suppress the release of EmGFP from the stalled ribosome after translation of the last codon (6,36). The results (Table 1, Figure 1B) show higher total fluorescent EmGFP production for circular plasmid than for linearized plasmid, in accord with an earlier report (22). Addition of anti-tmRNA to the linearized plasmid further reduces EmGFP production. Here the slightly higher value of total mature EmGFP synthesized (0.36/ribosome) vs. mature EmGFP cosedimenting with ribosomes (0.29/ribosome) arises from some combination of incomplete suppression of EmGFP release (i.e. a small number of ribosomes expressing multiple EmGFPs) and/or dissociation of some ribosome-bound EmGFP during either the reaction or ultracentrifugation. The fraction of active ribosomes (0.29), as measured by co-sedimenting fluorescent EmGFP, provides an important benchmark for evaluating the quality of different preparations and/or batches of CFPS kits, and of exogenous ribosomes that are substituted for endogenous ribosomes (see below). For other batches of the CFPS kit this fraction varied from 0.18 to 0.33, which is in reasonable agreement with previously reported results for SecM-stalled ribosomes with a protein of similar length (6) and somewhat higher than found in a previous single molecule experiment using similar methods (26).
High speed centrifugation can be used to remove endogenous ribosomes from the CFPS kit, resulting in a preparation, denoted the CFPS-ribosome kit, that is inactive in the EmGFP expression assay, with activity restored by addition of exogenous ribosomes. We examined the restoration of activity as a function of the extent of ribosome purification (Figure 2A and ‘Materials and Methods’ section), using the circular EmGFP plasmid, and determined that minimal purification, consisting of ribosome pelleting by high-speed centrifugation of crude S30 lysate, gave the highest restored activity. Accordingly this preparation, denoted S100P ribosomes, was used in assays comparing the activities of several exogenously added ribosomes, including wild-type MRE600 ribosomes, AM77 ribosomes lacking protein L11 (37) and AM77 ribosomes reconstituted with either wild-type L11 (AM77L11) or with an L11 variant labeled stoichiometrically at position 87 with Cy3 (AM77Cy3L11) (11) (Figure 2B). These results, showing that the lower activity of the AM77 ribosomes is partially restored by reconstitution with either wild-type or Cy3-labeled L11, indicate that derivatization of L11 with Cy3 does not interfere with translational activity, in accord with earlier results measuring other ribosomal activities (9,38,39). Addition of initiation factors improves the activity of these exogenously added ribosome preparations (Supplementary information 2B and Supplementary Figure S3A and B).
For the CFPS kit used for the experiments shown in Figure 2B, 0.18±0.02 of the endogenous ribosomes were active (determined as described above using the linearized EmGFP plasmid in the presence of anti-tmRNA), compared with 0.32±0.05 of the exogenously added MRE600 ribosomes and 0.09±0.01 and 0.10±0.04, respectively, for exogenously added AM77 and AM77L11 ribosomes. The lower fractions of active AM77-derived ribosomes account for the lower levels of EmGFP synthesis observed with these ribosomes (Figure 2B), although the intrinsic translation rate of active AM77-derived ribosomes is similar to that of wild-type ribosomes (see Supplementary Information 2A, and Supplementary Figure S2).
We next modified the EmGFP assay to permit comparison of the activities of added exogenous charged tRNA in supporting EmGFP expression. Below we detail our results with Phe-tRNAPhe, although the approach is general and has also been applied successfully to Val-tRNAVal and Lys-tRNALys. These experiments were performed using the circular EmGFP plasmid.
The principal challenge in the development of this modified assay was to prepare a CFPS-Phe kit (i.e. a kit depleted of all forms of Phe) such that synthesis of mature EmGFP was completely dependent on added exogenous Phe-tRNAPhe or Phe. This was accomplished by: (i) dialysis of the commercial CFPS lysate to remove all small molecules, including the amino acids; (ii) specific inhibition of Phe-amino-acyl tRNA synthetase (Phe-RS) with an active-site directed inhibitor; (iii) addition of a general protease inhibitor to prevent generation of Phe from protein breakdown; and (iv) adding back all of the small molecules required for protein synthesis with the exception of Phe (Supplementary Figure S3C). The ability of the resulting CFPS-Phe kit to produce detectable amounts of EmGFP was totally dependent on adding either exogenous yeast Phe-tRNAPhe (Figure 3A, Supplementary Figure S4A—similar results were obtained for E. coli Phe-tRNAPhe; Supplementary Figure S4B) or Phe (Figure 3B) with maximal EmGFP expression requiring higher concentrations of Phe (80µM) than of Phe-tRNAPhe (8–10μM) (Figure 3C and D).
The curves of EmGFP fluorescence in Figure 3A and B can be characterized by four parameters, a lag phase corresponding to all dark events preceding EmGFP maturation (tL), a region of high slope reflecting the maximum rate of fluorescent EmGFP formation (phase-1-slope, S1), the total fluorescent EmGFP synthesized in the first, rapid phase of reaction (phase-1-amplitude, A1), and a final region of lower slope (phase-2-slope, S2) corresponding to a slower, second phase. Each of the latter three parameters shows a strong Phe-tRNAPhe or Phe concentration dependence (Figure 3C and D, respectively). Both S1 and A1 increase nearly monotonically before reaching saturated values. S2 increases monotonically over the limited range of Phe-tRNAPhe concentrations employed, but goes through a maximum over the broader range of Phe concentration that was explored. In contrast, tL has only minor dependence on either Phe-tRNAPhe or Phe concentration. The overall maximal activities of the CFPS-Phe kit with added Phe-tRNAPhe (8-10µM) or Phe (80µM) were similar to one another (Supplementary Figure S3D), but reduced as compared with the unmodified CFPS kit, showing similar tL values but 2- to 4-fold reductions in the values of S1, S2, and A1 (Supplementary Table S1).
The CFPS-Phe kit makes very efficient use of added Phe-tRNAPhe. For a CFPS-Phe kit containing a total active ribosome concentration of 0.6µM, saturation of Phase-1-formation was reached by ~8μM yeast Phe-tRNAPhe (Figure 3C). As the encoded EmGFP has 14 Phe residues (2 in the N-terminal linker sequence and 12 in the original gene) the value of 8µM of added Phe-tRNAPhe found at saturation, in addition to the residual endogenous Phe-tRNAPhe (2µM) that we estimate to be present in the CFPS-Phe kit (see below), is just slightly above the expected stoichiometric requirement of 8µM Phe-tRNAPhe needed to produce one EmGFP per active ribosome. This result indicates an apparent Km for Phe-tRNAPhe incorporation at cognate codons that is <1µM, in accord with results derived from simpler model sytems (10,40,41). The apparent Km for Phe, estimated from the concentration dependence of either S1 or A1, is ~10–15µM. This value, which represents the first reported estimation of Km for an amino acid in a CFPS system, is considerably higher than the value for Phe-RS (2µM) determined in a highly purified system (42), perhaps reflecting competing binding to Phe-RS in the CFPS-Phe kit by near cognate amino acids and/or added Phe-RS inhibitor.
We developed a numerical simulation of a reaction kinetics model in order to gain additional understanding about the effects of exogenous Phe-tRNAPhe (see below) on the formation of EmGFP fluorescence using the CFPS-Phe kit (Figure 3A). This model includes 315 steps, which proceed in series, and include: a transcription initiation step, a transcription elongation step, a translation initiation step, 310 translation elongation steps, utilizing 296 non-Phe aminoacyl-tRNAs and 14 Phe-tRNAPhes according to the EmGFP sequence, and two fluorophore maturation steps (35). Each non-Phe translation elongation step was assigned the same pseudo-first-order rate constant (k1) and each Phe translation elongation step was assigned a second-order rate constant, k2 for endogenous Phe-tRNAPhe and for exogenous Phe-tRNAPhe. The pseudo-first-order rate process with rate constant k1 reflects the large excess of each of the non-Phe aminoacyl-tRNAs present in the CFPS-Phe kit while the second-order process, k2, reflects the limited availability of the added Phe-tRNAPhe.
In order to account for the rather small observed threshold value of exogenously added Phe-tRNAPhe (~1µM) that has to be exceeded in order to detect EmGFP fluorescence (Figure 3C), the model includes endogenous Phe-tRNAPhe that is not completely removed in preparing the CFPS-Phe kit and functionally heterogeneous ribosomes. If all of the ribosomes were equally active, small amounts of added Phe-tRNAPhe would be consumed by synthesis of incomplete, non-fluorescent chains, leading to a considerably higher threshold Phe-tRNAPhe concentration (Supplementary Figure S6). A final assumption is that protease and Phe-RS activities are incompletely inhibited in the CFPS-Phe kit, allowing a continual slow regeneration of the limiting reagent, Phe-tRNAPhe, that results in the slow second phase of EmGFP formation.
The kinetic model was used to simulate actual results obtained on adding varying Phe-tRNAPhe concentrations to the CFPS-Phe kit, as described below. Further details on the simulation may be found in Supplementary Information 4A.
We used the CFPS-Phe kit to compare the relative activities of various Phe-tRNAPhe variants in EmGFP synthesis. The Phe-tRNAPhes examined were E. coli and yeast, either unlabeled or labeled at dihydroU residues (16 and 17 in yeast or 16 and 20 in E. coli tRNAPhe) to a total stoichiometry of 0.8 – 0.9 fluorophores/tRNA (Table 2) with either Cy3, Cy5, or Cy5.5 (10). Variants were examined at one to three concentrations over a concentration range, 1–4µM (Figure 4A), for which both S1 and A1 are highly dependent on Phe-tRNAPhe concentration (Figure 3C).
Although the simulation model described above adequately fits the data using identical values of for both yeast and E. coli exogenous unlabeled Phe-tRNAPhes (equal to the k2 value for endogenous Phe-tRNAPhe), some variability in individual head-to-head comparisons caused slight differences in apparent activity, as is evident from Figure 4A. In contrast, the labeled Phe-tRNAPhes were consistently less active than the unlabeled Phe-tRNAPhes with respect to values of both S1 and A1 (Figure 4B and C, Table 2). A large increase in tL is associated with the use of Cy5-labeled yeast Phe-tRNAPhe, whereas tL is not strongly affected by the other Phe-tRNAPhes. The relative activities of labeled Phe-tRNAPhes are reduced more strongly at higher concentrations (Table 2), suggesting that high concentrations of the labeled Phe-tRNAPhe preparations are inhibitory. Such inhibition could be due, at least in part, to an increase in uncharged, labeled tRNAs in these preparations (Supplementary Figure S3E) that may offset the direct effect of raising Phe-tRNAPhe concentration.
Because of the apparent inhibition at high labeled Phe-tRNAPhe concentrations, only the time-courses of fluorescent EmGFP formation using 2µM exogenous labeled Phe-tRNAPhe (Figure 4B and C) were fit with the kinetic simulation model. The resulting values (Table 2) show that the activities of the labeled tRNAs, relative to E. coli Phe-tRNAPhe, fall in the order Cy5.5 (5-fold reduction) > Cy3 (10-fold reduction) > Cy5 (40–fold reduction). The order of activity found with these dyes suggests that activity loss results from a combination of steric bulk and hydrophobicity, since Cy3 is both smaller and less hydrophobic than Cy5, whereas Cy5.5, a dianion at neutral pH, is both larger and less hydrophobic than Cy5.
Plasmid-dependent [14C]-Phe incorporation into polypeptide during EmGFP synthesis provides an alternative measure of the relative activities of labeled Phe-tRNAPhe in protein synthesis. [14C]-Phe incorporation is less stringent than the EmGFP fluorescence assay, since it measures synthesis of partial and full-length EmGFP chains regardless of correct folding or chromophore maturation. Indeed, for the results presented in Table 2 using unlabeled E. coli or yeast Phe-tRNAPhe, only 35–40% of the [14C]-Phe incorporated into precipitable peptide chains was incorporated in full-length fluorescent EmGFP protein in the first 30min of the reaction, as determined by carrying out both analyses on the same sample. The relative [14C]-Phe incorporation levels are consistent with relative activities observed in ensemble measurements of polyPhe synthesis and single molecule translation of short stretches of model mRNAs using these same labeled tRNAs (10,11). Qualitatively, the relative [14C]-Phe incorporation levels showing Phe-tRNAPhe (Cy3) to be more active than Phe-tRNAPhe (Cy5) for both E. coli and yeast tRNAs parallel the order of relative activities found in the fluorescence assay measured either by or A1 values (Table 2).
Here we describe a convenient, fluorescence-based assay that, via adaptation of a commercially available bacterial CFPS kit, permits quantitative determination of the effects on the rate and stoichiometry of fluorescent EmGFP expression of replacing endogenous with exogenous components of the protein synthesis machinery. An important adjunct to this assay is the quantification of the fraction of active ribosomes in either the CFPS kit itself, or in a sample from which endogenous ribosomes have been removed (the CFPS-ribosome kit) and replaced. Approximately 20–30% of the ribosomes in the commercial CFPS kit are active in fluorescent EmGFP expression. By comparison, wild-type MRE600 ribosomes prepared by us show ~30% activity, whereas the fractional activities of the mutant AM77 ribosomes which lack protein L11, even when supplemented with L11, are distinctly lower (~10%).
As described above, replacement of endogenous ribosomes is quite facile, since exogenous ribosomes prepared directly from crude cell extracts (‘S100P’ ribosomes) confer the highest activity when added to the easily prepared CFPS-ribosome kit. Replacement of endogenous Phe-tRNAPhe is somewhat more demanding, but relatively straightforward using the optimized procedures detailed in ‘Materials and Methods’ section. In order to selectively remove Phe-tRNAPhe, we elected to prepare a CFPS-Phe kit in which the endogenous tRNAPhe is retained, but Phe is depleted and Phe-RS is inhibited. With the CFPS-Phe kit, fluorescent EmGFP expression is totally dependent on either added Phe (Figure 3B) or added Phe-tRNAPhe, at much lower concentration (Figure 3A). An alternative approach for preparing a CFPS-Phe system, which we are currently pursuing, utilizes PURExpress® (New England Biolabs), a cell-free transcription/translation system reconstituted from purified E. coli components, including each of the tRNA synthetase enzymes (43). A custom-made PURExpress® mixture should essentially eliminate the residual Phe-tRNAPhe and Phe-RS content present in a CFPS-Phe kit.
Our primary goal in developing adaptations of CFPS kit assay for the expression of fluorescent EmGFP was to permit determination of the effects on translational activity of fluorescent labeling of components of the protein synthesis machinery, in particular ribosomes and tRNAs, since such labeling is used extensively in both ensemble and single molecule studies of the mechanism of protein synthesis (12–15). The results showing that dye-labeled Phe-tRNAPhes have substantially lower activity than unlabeled Phe-tRNAPhe in supporting full-length protein synthesis highlight the need to explore alternative labeling strategies to produce labeled tRNAs with higher intrinsic activities. Such strategies could include using tRNA transcripts so as to be able to direct labeling to a unique DHU position (44) as opposed to native tRNAs, for which labeling is distributed over all DHU positions (45,46); using less hydrophobic fluorophores; and introducing fluorophores at other than DHU positions (47–49).
In addition to meeting our primary goal, continuous monitoring of the formation of fluorescent EmGFP by simple or modified CFPS kits provides a general, radioactivity-free approach, amenable to high-throughput screening, for evaluating effects on the efficiency of protein synthesis of various additions, subtractions or substitutions to the protein synthesis machinery. These include (i) any kind of tRNA, rRNA or ribosomal protein variation, including mutation or enzymatic or chemical modification; (ii) addition of agents affecting transcription, translation, or protein folding (e.g. antibiotic screening effects on translation could be separated from those on transcription by initiating EmGFP synthesis with added mRNA, transcribed separately, rather than with added DNA); (iii) substituting amino acid analogues for native amino acids, whether measured by supplementing a CFPS-aminoacid kit with the amino acid analogue or with a tRNA charged with the analogue (50). In some experiments, suitable controls would be needed to exclude possible artifacts due to direct effects on EmGFP fluorescence. Finally, a CFPS-aminoacid kit, reconstituted with an isotopically labeled amino acid, could be used to prepare isotopically labeled proteins for IR and NMR studies.
Supplementary Data are available at NAR Online: Supplementary Tables S1–S3, Supplementary Figures S1–S6, Supplementary Information Files S1–S2 and Supplementary Reference .
National Institutes of Health (GM080376 to B.S.C., Y.E.G.); Human Frontier Science Program fellowship (to G.R.). Funding for open access charge: National Institutes of Health (GM080376).
Conflict of interest statement. Y.E.G. and B.S.C. are paid consultants for Anima Cell Metrology.
We thank Dr Olga Lozynska in Professor Scott Diamond’s group at Penn for her help with the plate reader.