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Journal of Nanomaterials
Volume 2013 (2013), Article ID 468105, 9 pages
A Novel Complex: A Quantum Dot Conjugated to an Active T7 RNA Polymerase
1Niels Bohr Institute, University of Copenhagen, 2100 Copenhagen, Denmark
2Institute of Biology, Eötvös Loránd University, Budapest 1053, Hungary
3Institute of Biology, University of Copenhagen, 2200 Copenhagen, Denmark
Received 28 January 2013; Accepted 17 April 2013
Academic Editor: Christophe Merlin
Copyright © 2013 Mette Eriksen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
To perform single-molecule studies of the T7 RNA polymerase, it is crucial to visualize an individual T7 RNA polymerase, for example, through a fluorescent signal. We present a novel complex combining two different molecular functions, an active T7 RNA polymerase and a highly luminescent nanoparticle, a quantum dot. The complex has the advantage of both constituents: the complex can traffic along DNA and simultaneously be visualized, both at the ensemble and at the single-molecule level. The labeling was mediated through an in vivo biotinylation of a His-tagged T7 RNA polymerase and subsequent binding of a streptavidin-coated quantum dot. Our technique allows for easy purification of the quantum dot labeled T7 RNA polymerases from the reactants. Also, the conjugation does not alter the functionality of the polymerase; it retains the ability to bind and transcribe.
RNA polymerase (RNAP) is an enzyme that catalyses transcription. It shall balance two tasks: binding to specific sites on DNA where transcription is initiated (promoters) and the ability to disengage at the termination signals. Proteins and other cofactors can inhibit or recruit RNAPs to DNA, thus regulating the initiation process.
Several families of RNAPs exist which differ in their molecular characteristics. The viral T7 RNA polymerase is a single subunit RNAP (98 kDa)  characterized by extreme promoter specificity  and a very low error rate . The T7 family of RNAPs is structurally and evolutionary distinct from the multisubunit family of RNAPs. T7 RNAP allows specific high-level transcription and expression of cloned genes ; therefore, it is a key enzyme in the production of recombinant proteins and also in several in vitro molecular biology applications [5, 6]. Such applications include the generation of large quantities of RNA transcripts for translation, synthesis of tRNA, rRNA, RNA virus genomes, ribozymes, microarray targets , production of substrates for RNA splicing , RNA secondary structure, antisense RNA, and RNA-protein interaction studies. The T7 RNAP is suitable for homogeneous radioactive or nonradioactive labeling of single-stranded RNA, and it plays an important role in technologies based on RNA and DNA hybridization . Tight regulation of T7 RNAP expression is possible and T7 systems are therefore used for the production of otherwise deleterious protein products .
A wide variety of assays are designed to study the diffusive or directed translocation of molecular motors. In order to visualize or manipulate the individual motor, it is typically conjugated to a fluorescent probe or a dielectric particle. An effective conjugation, which does not alter the activity of the enzyme, is absolutely essential in order to obtain trustworthy results.
Due to their high quantum yield and large photostability [11–14] colloidal quantum dots (QDs) are a particularly good choice as labels for molecular motors. QDs have been used, for example, to track the motility of individual receptors in a cell membrane , to track individual bacteriophages infecting bacteria  and to monitor individual proteins diffusing on DNA [17, 18]. Individual colloidal QDs can even be optically manipulated  and excited by the trapping laser through two-photon absorption , thus enabling both visualization and manipulation through specific attachment of a single QD. For these reasons, it is highly desirable to devise a method to specifically attach QDs to individual molecular motors. QDs can be taken up by living cells  and are nontoxic when encapsulated. Hence, they also have potential for in vivo studies of, for example, the action of molecular motors.
Here, we devise a technique to specifically label individual T7 RNAPs by QDs through a biotin-streptavidin bond, and we show that the QD-functionalized T7 RNAP (QD : T7RNAP) retains activity. Previously, activity was proven of a QD-labelled E. coli RNAP , and activity was proven of T7 RNAP bioconjugated to polystyrene beads ; however, to our knowledge this is the first report of QD labelling of viral T7 RNAPs that retain activity after QD marking. Moreover, our applied purification technique is simple, inexpensive, and very efficient.
2. Materials and Methods
2.1. In Vivo Biotinylation and Purification of T7 RNAP
Our construct was based on plasmid pBH161 which was a generous gift from William T. McAllister, Department of Biochemistry, University of New Hampshire. Plasmid pBH161 encodes a T7 RNAP His-tagged N terminally . We further tagged the enzyme N terminally with the GLNDIFEAQKIEWH sequence, referred to as a biotag, which was recognized by biotin ligase and biotinylated at a single lysine in vivo  (Figure 1). The DNA sequence encoding the Bio-tag was synthesized by PCR using three overlapping primers: 5′-ATCACCATGGGTAGCAGCGGCCTGAACGACATCTTCGAAGCTCAGAAAA-. -ATCTTCGAAGCTCAGAAAATTGAATGGCACGGCAGCTCTCATCATCATCATCATCA
The synthesized DNA fragment was digested by XhoI and NcoI and inserted between the XhoI and NcoI sites in pBH161 upstream of the sequence encoding the His-tag; the resulting plasmid was denoted as pBioT7. Bio-His-tagged T7 RNAP (Bio-T7 RNAP) was expressed in the E. coli strain BL21Star (Invitrogen) containing the plasmids: pBioT7 and pBirA (Avidity), which expresses biotin-holoenzyme-synthetase activities. Enzymes were purified from the lysate using Ni2+-agarose beads (Qiagen) and eluted with 80 mM imidazol.
2.2. Quantification of Biotinylation of T7 RNAP
To quantify the amount of Bio-T7 RNAPs, purified Bio-T7 RNAPs were mixed with SoftLink Soft Release Avidin Resin (Promega) and allowed to bind for 1 hour at room temperature. The mixture was loaded on Poly-Prep Chromatography Columns (Bio-Rad) and the flow-through was collected. The column was washed with 10 bed volumes of buffer (20 mM Tris-HCl pH 7.9, 0.5 M NaCl, 0.05% (w/v) Tween 20). Samples of the flow-through, the washed fraction, and the matrix-bound fractions were loaded on a 4–12% NuPAGE gel (Invitrogen) along with a molecular weight marker (SeeBlue Plus2, Invitrogen). The control protein (Phage 16-3 repressor, C16-3) was not biotinylated. After electrophoresis the gel was stained with Coomassie Brilliant Blue.
2.3. Estimation of Concentration of Biotinylated T7 RNAPs
We used the ExPASy ProtParam tool (expasy.org)  to calculate the theoretical extinction coefficient of the Bio-T7 RNAP to 145760 1/M*cm. The absorbance was measured using a NanoDrop spectrophotometer (ThermoScientific). The enzyme preparation also included impurities (Figure S1, see supplementary material available online at http://dx.doi.org/10.1155/2013/468105) of unknown extinction coefficient. The approximate enzyme concentration was estimated using the measured absorbance and Beer-Lamberts equation.
2.4. Verification of Activity of Biotinylated T7 RNAPs
The in vivo biotinylated T7 RNAPs were immersed in a reaction mixture containing 2 ng/μL 1,000 bp DNA template with T7 promoter and terminator, transcription buffer (40 mM Tris-HCl pH 7.9, 6 mM MgCl2, and 10 mM NaCl), 2 mM spermidine, 10 mM DTT, 2 mM of each rNTP, 2 units/μL RNasin, and 2.6 μM Bio-T7 RNAP. The reaction mixture was incubated at for 1 hour and loaded onto a 1.8% agarose gel and stained with ethidium bromide.
2.5. Formation of QD : T7RNAP Complexes
The Bio-T7 RNAPs were attached to QDs in the following manner. In a final volume of 30 μL 0.13, 0.091, or 0.052 nmol of the Bio-T7 RNAP were mixed with 10 mM DTT, transcription buffer, and 0.01 nmol streptavidin-coated QDs (Qdot605, Invitrogen). The mixture was left at for 1.5 hour allowing the streptavidin-biotin bonds to form. Parallel controls consisted of the same solution with Bio-T7 RNAPs but without QDs present.
2.6. Purification of QD : T7RNAP Complexes
In order to purify the QD : T7RNAP complexes 20 μL transcription buffer was added to the QD : T7RNAP and control solutions. Each of the final 50 μL reactions was transferred to 25 μL avidin resin, prewashed and centrifuged. The resin was resuspended, and put on a shaker at for 1 hour. The avidin and QD : T7RNAP suspensions were filter-centrifuged (pore size 0.45 μm, Pierce), only allowing the QD : T7RNAP and the free QDs to be in the flow-through, which was collected for an activity test (Figure 2). The avidin resins were washed with 100 μL transcription buffer and resuspended in 10 μL transcription buffer and also collected for an activity test.
2.7. Activity of QD : T7RNAP Complexes and Avidin-Bound RNAPs
A 1,000 bp T7 RNAP transcription template was made by PCR on pJT512 (the 11/6 construct of Tholstrup et al.2012 ). Forward primer was TH414: -TAATACGACTCACTATAGGGAGAGTATACCTCTCAGTTGGGTG-
(underlined is overhang containing T7 promotor) and the reverse primer, TH412, had the sequence: 5′-ATAATTCGCGTCTGGCCTTC.
This template supports a 1000 nt long transcript from the promoter to the end of the fragment. All activity tests were made with this template, except in Figures 4(b) and 4(c) where the template pMAS30 (plasmid encoding upstream lacZ riboprobe ), digested with SacI, was used. This T7 RNAP template supports a 830 nt long transcript.
Activity tests were performed of both the flow-through containing QD : T7RNAP complexes and of the washed avidin resin containing Bio-T7 RNAPs bound to the avidin resin. The reaction mixture (10 μL) contained 2 ng/μL, 1,000 bp DNA template with a T7 promoter, transcription buffer, 2 mM spermidine, 10 mM DTT, 2 mM of each rNTP, 2 units/μL RNasin, and 6 μL of collected QD : T7RNAP solution. The reaction mixture was incubated at for 1 hour and loaded on a 1.8% agarose gel. The two controls consisted of 0.026 nmol Bio-T7 RNAPs in transcription buffer and 1 pmol QDs in transcription buffer.
As each QD is coated with 6–8 streptavidins (Invitrogen), the average number of Bio-T7 RNAPs bound to each QD can be controlled by adjusting Bio-T7 RNAP and QD concentrations. The RNA product of the activity test should not derive from free Bio-T7 RNAPs. In order to find the amount of RNA product originating from free Bio-T7 RNAPs, controls undergoing the same procedure as the samples, but with no QDs, revealed the amount of free Bio-T7 RNAPs escaping the avidin resin in the flow-through. In this way the concentrations of Bio-T7 RNAPs and QDs yielding optimal working conditions, that is, an absolute minimum of free Bio-T7 RNAPs, were found.
2.8. T7 RNAP Streptavidin Control
A gel filtration was performed in order to exclude the possibility that active QD : T7RNAPs were only attached to streptavidin (and not to a QD). In this experiment 0.385 nmol Bio-T7 RNAP was mixed with 0.075 nmol QDs (Bio-T7 RNAP : QD 5 : 1) in a final volume of 110 μL, and the solution was left at for 1.5 hour to allow the formation of complexes. The solution was filtered through a Superose 6 10/300 GL column on BioRad BioLogic DuoFlow at a flow rate of 0.5 mL/minute transcription buffer. 0.5 mL fractions were collected with BioRad BioLogic BioFrac Fraction Collector. Controls without QDs were processed similarly using 2.137 nmol and 0.385 nmol Bio-T7 RNAP, respectively.
An activity test was performed on the gel filtration fractions. To this end 1/50 (10 μL) of each collected fraction was supplemented to a final volume of 12.1 μL with spermidine, DTT, rNTPs, and RNAse inhibitor (at concentrations described for the previous activity tests) and ~20 ng DNA. The samples were incubated at for 2.5 hours before electrophoresis on 1.8% agarose gels. The 2.137 nmol Bio-T7 RNAP control was tested with ~115 ng PCR-amplified DNA template from pJT512.
2.9. Single Molecule Assay
A 3,250 bp piece of -DNA was synthesized by PCR using the primers: -TTTTGAATTCAAAAAACCCCTCAAGACCCGTTTAGAGGCCCCAA GGGGTTCTCATGCTGAAAACGTGGTGTACCGGC-; -TTTTTTAAGCTTGGACCTATCTGCCCGTTCGTCCCGTCGTT-.
This DNA piece was inserted between the EcoRI and HindIII of the plasmid pGEM4Z (Promega) downstream of the T7 promoter. Using this plasmid pLJP1 as a template, a ~3,000 bp DNA was constructed with biotin and digoxigenin labels at the ends using the following primers: -Bio-TGTGATGCTCGTCAGGGGGGCGGAGC- -Dig-TTCTCATGCTGAAAACGTGGTGTACCGGC-.
The DNA product was purified with QIAquick Gel Extraction Kit. At ~500 bp from the biotinylated end, the DNA construct had a T7 promoter. There was no terminator site present.
A perfusion chamber was made by placing parafilm forming a 20–25 μL well on a 60 × 24 mm glass slide and adding a 50 × 24 mm glass slide as lid. The chamber was heated such that the parafilm melted to the glass surfaces. To coat the surface with antidigoxigenin 20 μg/mL antidigoxigenin in TE (10 mM Tris-HCl (pH 8), 1 mM EDTA) was flushed into the chamber and left at overnight or at least 1 hour at . To minimize unspecific bindings to the glass surface transcription buffer containing 2 mg/mL -casein was flushed through the chamber and incubated for 1 hour at . 10 nM of the DNA solution was flushed into the chamber and incubated for 30 minutes at such that the digoxigenin-labeled end of the DNA tether could bind to the antidigoxigenin-coated surface. 2 mg/mL -casein in transcription buffer was flushed into the chamber and left at for 30 minutes to block unspecific bindings. Finally, QD : T7RNAP complexes (2.6 nM Bio-T7 RNAP and 1 nM QDs) in transcription buffer with 2 mg/mL BSA, 2 mg/mL spermidine, 2 mM of each ribonucleotides, and 10 mM DTT were flushed into the chamber, and the chamber was sealed with vacuum grease. The controls were processed similarly but without ribonucleotides in the transcription buffer.
The samples were investigated using an inverted Leica microscope. A mercury lamp was focused with an oil immersion objective (Leica HCX PL APO 100 × NA = 1.4 oil, CS). To image the light emitted from the 605 nm QD we used a custom made filter cube (Leica HQ420/40x + 1064, z440/1065rpc, and HQ605/40m-2p) which allowed the 420 nm light from the mercury lamp to be reflected up to the sample and only allowed the emitted 605 nm light to be transmitted to the EMCCD camera (Ixon, Andor). The images were analyzed with ImageJ and custom made Matlab routines. In addition, we performed centroid tracking of the tethered QDs using the ImageJ tracking routine Spottracker2D .
3. Results and Discussion
3.1. In Vivo Biotinylation
The T7 RNAPs were biotinylated in vivo with a procedure that parallels the method used for biotinylating a lambda phage subsequently labeled by a QD . The biotinylated T7 RNAPs were purified using an agarose bead assay. The amount of biotinylated T7 RNAPs was quantified using an avidin-coated resin and estimated to be 95–99% of the total (Figure S1).
After in vivo biotinylation of T7 RNAPs we tested that they were still active. The activity was verified by inspecting the strong band at the expected weight of the product in lane 4 (Figure 3, red arrow). As native T7 RNAP did not bind the avidin resin, seen by comparing lane 3(F) to lane 3(A) (Figure S3), the conjugation of the avidin resin and Bio-T7 RNAPs is mediated by the biotin-streptavidin bond only. The QD : T7RNAP complexes were formed by mixing the Bio-T7 RNAPs with streptavidin-coated QDs. In order to purify the QD : T7RNAP complexes they were mixed with an avidin resin, with the goal of capturing possible Bio-T7 RNAPs which did not bind to QDs. The suspension was filter centrifuged using a 0.45 μm filter (Figure 2) and the QD : T7RNAP complexes would be present in the flow-through. Free QDs would also pass the filter and be present in the flow-through as well as possible streptavidin:T7RNAPs released from the QDs. There has been earlier attempts to tag T7 RNAPs , but the activity of the protein, when conjugated to a QD, was not confirmed.
3.2. Activity of Ensembles of QD : T7RNAP Complexes
The activities of the purified QD : T7RNAP complexes and the corresponding controls without QDs were investigated using normal gel electrophoresis (Figure 3). The RNA products (red arrow) from the flow-through (F) and avidin resin (A) are shown for Bio-T7 RNAP concentrations in the initial binding mixture of, respectively, 0.13, 0.091, and 0.052 nmol in lanes marked 1, 2, and 3 and QD concentrations of 0.01 nmol. This corresponds to QD : T7RNAP ratios of about 1 : 13, 1 : 9 and 1 : 5, respectively. The corresponding controls, without QDs, are shown in lanes marked C1, C2, and C3. There is a clear band denoting the existence of an RNA product in all lanes originating from QD : T7RNAP complexes and in all control lanes, albeit, only in the avidin resin (A) of the latter. This verifies that the RNA product present, for example, in lane 3 (F) originated from QD : T7RNAP complexes only since no RNA product is present in the flow-through of C3. This also shows that the surplus of free Bio-T7 RNAPs is efficiently captured by the avidin resin. Hence, we conclude that the Bio-T7 RNAP is indeed active when bound to a QD.
It is clear from lanes 1, 2, and 3 that the majority of the QDs passed the 0.45 μm filter and showed up on the gel in the F columns as two distinct bands (blue arrow) at 1500–1700 bp as earlier reported . Interestingly, the QDs with Bio-T7 RNAPs attached migrate further than the QD alone; to see this compare lane 5 (yellow arrow) to lanes 1, 2, or 3 (F) (blue arrow). This is probably because the net charge of the Bio-T7 RNAP at pH 8.5 (pH of the agarose gel buffer) is −5, and therefore the QD : T7RNAP complex migrates faster towards the anode during electrophoresis than the free QDs. The agarose gel pore size was relatively large in comparison to the size of the approximately spherical QD : T7RNAP complex. Hence, the fact that one or possibly more charged Bio-T7 RNAPs are attached and thereby cause the complex to move faster in the field has a larger influence on the overall migration than the incremental increase in effective diameter .
QDs are only present in the flow-through (F) of lanes 1, 2, and 3 (Figure 3), confirming that the majority of the QDs passed the filter and did not stick to the avidin resin. On the basis of the intensities of the bands originating from the RNA products of F and A we estimated a ratio 3-4 : 1 of RNAPs to QDs. This ratio is in accordance with a recent report on biotin binding to the same type of QDs .
The total amount of RNA product in the presence of QDs, lane 3, corresponds well with the RNA product in the control without QDs, lane C3 (same initial Bio-T7 RNAP concentrations). The intensities of the bands with RNA product (red arrow) in lane 3 (F + A) were quantified (ImageJ, Gel Analyser) and compared to the band with RNA product (red arrow) in C3. The two samples differed in intensity by ~5% only; hence, the Bio-T7 RNAP retained similar activity whether bound to QDs or to the avidin resin. The fact that the Bio-T7 RNAP also binds very well to avidin-coated agarose beads (Figure 3 lanes C1–C3) while retaining enzymatic activity proves the generality of the method; the Bio-T7 RNAPs retain activity though bound to other types of avidin-coated handles than a QD.
To estimate the activity loss due to QD conjugation we first determined if our activity assay responded to different polymerase concentrations (Figure S2). Next, we compared the activity of the QD : T7RNAP complex to the nonconjugated Bio-T7 RNAP (lane 1 (F + A) to lane 4 in Figure S3) and corrected for dilutions of Bio-T7 RNAP in lanes 1 to a concentration of approximately 0.013 nmol. This comparison showed that the QD : T7RNAP complex lost at most ~15% of its activity in the experiment shown in Figure S3. However, upon repeating the experiment 21 times with an independently purified protein batch, we found an average activity loss of ()% (mean ± STD) upon QD conjugation. Our activity test of QD-bound RNAPs is an indirect method of measuring the purity of complexes compared to gel purification . However, running the complexes through an avidin resin is still reliable, time saving and requires very little preparation.
3.3. Gel Filtration of QD : T7RNAP Complexes
To exclude the possibility that the active Bio-T7 RNAP was only bound to streptavidin (and not to QDs) released from the stock solution of streptavidin-coated QDs, we mixed Bio-T7 RNAP and QDs in a molar ratio of 5 : 1 and performed a gel filtration on a Superose 6 column (Figure 4). This type of column facilitates the separation of high molecular weight substances and molecules in the particle size range relevant for ribosomes and QDs. The goal of this experiment is to compare the Bio-T7 RNAP activity in the fractions where QDs eluted to the activity in the fractions where streptavidin:Bio-T7 RNAP is expected to elute. In the experiment three different gel filtrations were performed, two controls without QDs with different Bio-T7 RNAP concentrations and one with QDs present. The two controls without QDs were performed using 2.137 nmol Bio-T7 RNAP (Figure 4(a)) and 0.385 nmol Bio-T7 RNAPs (Figure 4(b)), respectively. The Bio-T7 RNAPs elute at 37 minutes (fraction 25) clearly visible in Figure 4(a) and just visible in Figure 4(b). Figure 4(a) shows where free Bio-T7 RNAP elute, while Figure 4(b) is a control to Figure 4(c), which shows the signal that can be obtained with this low amount of Bio-T7 RNAP. Another important reason to use a low concentration of QDs for the gel filtration was that these experiments required a very large amount of QDs (~75 μL) in comparison to the other experiments described above (which each used 10 μL). As QDs are still rather expensive, it makes sense to perform the experiment with as small an amount as possible (as done in the experiments depicted in Figures 4(b) and 4(c)). It is unlikely that the streptavidin tetramer would be able to bind more than two molecules of biotin-labelled T7 RNAP due to steric hindrance [34, 35], and the complex would maximally obtain a molecular weight of 60 kDa (Streptavidin) + 2 × 103 kDa (T7 RNAP) = 266 kDa. Such a complex should therefore elute approximately at 28 minutes (fraction 19), much later than the observed QD : T7RNAP activity that peaked in fractions 14-15 (inset of Figure 4(c)). The Bio-T7 RNAP peak is not visible and the corresponding activity in fraction 25 was very low compared to the early fractions. The peak at 50 minutes is caused by oxidized DTT from the storage buffer. Due to a relatively large spread in QD sizes (Figure S4) the Bio-T7 RNAP activity peak actually extended up to fraction 5 where the largest QDs appeared. Hence, we conclude that the activity observed was indeed from QD : T7RNAP. These results also exclude the possibility that the activities seen in our other assays originate from residual T7RNAP unbound to QDs. Because we see the same overall amount of RNA in fraction 6–17 of Figure 4(c) as is fraction 22–28 of Figure 4(b), we conclude that the activity of the complex is comparable to the activity of free Bio-T7 RNAP.
3.4. Activity of Single Molecule QD : T7RNAP Complexes
As the QD : T7RNAP complex has a large potential for single-molecule investigations, we also tested its activity in a typical single-molecule assay, the tethered particle assay. In this assay a double-stranded DNA tether (~3,000 bp) was specifically anchored to a surface with the free biotinylated end bound to a reporter particle, a streptavidin-coated QD. The DNA tether had a T7 promoter sequence 500 bp from the free end, and this promoter was directed towards the glass surface. The experiment and a control were conducted as sketched in Figures 5(b) and 5(c), respectively. Intensity images of DNA tethers on the coverslip surface (Figures 5(d) and 5(e)) were collected with wide-field fluorescence microscopy and a sensitive camera.
Prior to every experiment we located the DNA tethers with the reporter QD and tracked the diffusive behavior through time to find the subpixel coordinates. The magnitude of the tethered particle motion contains information on the overall length of the tether. Therefore, the diffusion was used to verify that the observed QDs were indeed attached to a DNA tether of ~1 μm length and not, for example, an agglomerate of -casein which, most likely, has a shorter tethering length. To this end we measured the root-mean-square displacement: Here, , is the position of one of the two orthogonal dimensions of the projected surface plane, is the mean position, and is the number of data points in the time series. The root-mean-square displacement of QDs attached to the free end of the DNA tether was measured: = 233 nm ± 56 nm (mean ± STD) (). The result is in accordance with the one reported for a QD attached to a DNA tether of similar size .
For the actual experiment QD : T7RNAP complexes were added to the sample together with the required ribonucleotides (NTPs). Individual QD : T7RNAP complexes thus attached at the promoter site and started transcription along the DNA tether. As there was no transcription termination sequence, the QD : T7RNAP complexes were prone to accumulate on the DNA tether close to the glass surface. In the control no NTPs were present (−NTP); hence, it was unlikely that any QD : T7RNAP complexes would attach to the promoter or start elongating. The only fluorescent signal expected from the control was that originating from a streptavidin-coated QD attached to the biotinylated end of the DNA tether (Figure 5(e)).
In the experiments with the elongating QD : T7RNAP complexes (+NTP) the spots on the surface were significantly more intense than in the control experiment (−NTP). Probably because the luminescent spots in the experiments originated from a single DNA tether with multiple QDs attached, only one QD would attach to a DNA tether in the control experiments. As the DNA tether itself performed thermal fluctuations in and out of the focal volume and the QD also exhibited blinking, the resulting intensity time series (with total length ~200 s) had significant intensity fluctuations. In the analysis we used the window of 20 frames (~5 s) of each time series around the maximum intensity. The average intensity, , of the window was normalized to the intensity average of a time series originating from the control (−NTP), . The measured values of both for the experiment (red bars) and for the control (green bars) are shown in Figure 5(a). The intensity distribution of the control is very narrow and peaks around a value of 1, consistent with the expectation that only a single QD would attach to the tether. The intensity distribution of the experiment (+NTP) is significantly broader, scattered, and consistent with an average accumulation of 5 QDs per tether (at a concentration of 200 nM Bio-T7 RNAPs). Hence, we conclude that the individual QD : T7RNAP complexes are indeed active; in the presence of NTP they bind to the promoter and accumulate on the DNA tether.
We showed that the viral T7 RNAP could easily be efficiently biotinylated while retaining activity. In addition, we showed that upon attachment of a streptavidin-coated QD the QD : T7RNAP complex still retains activity. In particular, we showed how to purify QD : T7RNAPs from a solution of unbound RNAPs. As the conjugation and purification assays presented in this study were simple and highly efficient, the devised technique is recommendable for attachment and purification of QDs to Bio-T7 RNAPs. In comparison to the E. coli RNAP the viral T7 RNAP is simple as it only consists of a single polypeptide chain and has a short promoter recognition sequence. The simplicity of the T7 RNAP as well as its efficiency has paved the way for high production of specific protein products . Anyhow, only few single-molecule investigations of the T7 RNAP exist [37–40] in comparison to the detailed knowledge obtained on the single molecule level concerning the fundamental properties, for example, transcription velocity, stalling force, pausing events, backtracking, of E. coli RNAP. With the techniques here presented it will be possible to uncover the action of T7 RNAP even at the single-molecule level.
The authors acknowledge support from Jesper Tholstrup and thank Kaj Frank Jensen for introducing them to gel filtration. The work was financed through the University of Copenhagen Excellence Program.
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