Holger
Bußkamp
,
Ellen
Batroff
,
Andrea
Niederwieser
,
Obadah S.
Abdel-Rahman
,
Rainer F.
Winter
,
Valentin
Wittmann
and
Andreas
Marx
*
Department of Chemistry and Konstanz Research School Chemical Biology, University of Konstanz, Universitätsstrasse 10, 78457 Konstanz, Germany. E-mail: andreas.marx@uni-konstanz.de
First published on 22nd July 2014
Many applications in biotechnology and molecular biology rely on modified nucleotides. Here, we present an approach for the postsynthetic labelling of enzymatically synthesized vinyl-modified DNA by Diels–Alder reaction with inverse electron demand using a tetrazine. Labelling proceeds very efficiently and supersedes several known approaches.
For the postsynthetic modification of enzymatically synthesized DNA via DARinv (Fig. 1A) we envisioned 7-vinyl-7-deaza-2′-deoxyadenosine (dvinA) and 5-vinyl-2′-deoxyuridine (dvinU) (Fig. 1B) as nucleoside analogues bearing the vinyl group at the 7 or 5 position, respectively. The vinyl group is a very small modification that might render nucleosides into dienophiles for labelling by DARinv. In both cases the reactive group points towards the major groove of the DNA duplex and thus should be accessible by labelling reagents. The nucleosides were synthesized according to known procedures.14 As the reaction partner in the Diels–Alder reaction a known biotinylated tetrazine derivative (Fig. 1B) was used.13
To test the ability of the nucleosides to undergo DARinv with tetrazines, we determined the second-order rate constants k2 (Fig. S1, ESI†). dvinA undergoes DARinv with a constant k2 of 0.140 (±0.001) (L mol−1 s−1) and dvinU with a rate constant k2 of 0.010 (±0.0002) (L mol−1 s−1). The kinetic rate constant of dvinU is comparable to a recent report.15 We focused on dvinA in this study, as the DARinv proceeds 14-fold faster than the reaction with dvinU. Furthermore, the rate constant of dvinA is about 10-fold higher than that of the reaction of terminal alkenes with tetrazines, which has been reported for efficient labelling.13 In comparison to other prominent labelling reactions, the DARinv using dvinA proceeds faster than the Staudinger ligation16 or the strain-promoted azide–alkyne cycloaddition of dibenzocyclooctyne.17 Thus, labelling with dvinA and tetrazines appears to be promising for further applications.
The differences in the reactivity of the nucleobases might be explained by their different electronic properties. To gain further insights, we calculated the frontier orbitals of the tetrazine and the vinylated nucleobases and evaluated the energy difference of the interacting orbitals as an estimate for the reactivity.18 We found that the energy difference between the interacting orbitals (LUMO + 1 of the tetrazine, HOMO of the nucleobases; Fig. S2, ESI†) of the tetrazine and dvinU is larger by 0.55 eV than the difference between the corresponding orbitals when considering dvinA. The smaller energy difference can explain the higher reactivity of dvinA in comparison to dvinU.
Encouraged by these results, we synthesized dvinATP by phosphorylation as described in ref. 19. We tested the acceptance of the nucleotide analogue by KlenTaq DNA polymerase and conducted primer extension reactions (PEX) using a radioactively labeled primer strand. We employed standard conditions for primer extension reactions as they have been reported before.9a,b The nucleotide analogue was incorporated efficiently into the DNA strand. A full length product was observed in all cases and no stalling of the polymerase during incorporation of the modified nucleotide took place under the employed conditions, indicating efficient processing of the modified building block by the DNA polymerase.
Next, we tested if the incorporated modification can engage in DARinv in double stranded DNA (dsDNA). The primer extension product was incubated with tetrazine 1, bearing a biotin moiety. The DNA was used in low concentrations (0.9 μM) while an excess of labelling reagent (1.7 mM) was used. After purification via gel filtration, an aliquot was incubated with streptavidin. All samples were analyzed by denaturing polyacrylamide gel electrophoresis (PAGE). dvinA embedded in dsDNA undergoes DARinv with the biotinylated tetrazine derivative 1, indicated by the change in the migration of the product by PAGE analysis (Fig. 1C). Further control reactions point out that only when dvinATP was used as the substrate and dvinA was incorporated, the large shift of the product migration was detected by PAGE analysis after subsequent incubation with biotinylated tetrazine 1 and streptavidin.
Next, we investigated the efficiency of the reaction by varying the reaction time (Fig. 2). Interestingly, the starting material was almost completely consumed within 10 minutes. During longer incubation times another band appears that might be derived from the oxidation of the Diels–Alder reaction product, as it is known that dihydropyridazines easily oxidize to pyridazines in the presence of oxygen.13
Next, we investigated the dependence of the reaction efficiency on the concentration of the labelling reagent. Therefore, the product of the primer extension reaction in the presence of dvinATP was incubated with increasing concentrations of tetrazine 1. As an excess of tetrazine was applied, the reaction follows the kinetics of pseudo-first order. We stopped each of the reactions after different time points and analyzed the reactions by PAGE. Interestingly, when 22 μM labelling reagent is present, conversion to the reaction product occurred only to a minor extent even after prolonged reaction times (2 h). When 90 μM labelling reagent is used, after 2 hours about 70% of the starting material has been converted to the reaction product. Upon applying 450 μM tetrazine 1 about 70% conversion took place after 30 minutes and after 1 hour no starting material was detected anymore. To gain deeper insights, we performed kinetic studies of the DARinv on the DNA duplex (Fig. S3, ESI†). We estimated the second order rate constant k2 of 0.42 (±0.03) (L mol−1 s−1). This constant is 3-fold higher than for the nucleoside. This increase in the reaction rate might originate from the polar microenvironment in the major groove, in which the Diels–Alder reaction takes place, as it has been reported that Diels–Alder reactions are accelerated in polar solvents.20 Furthermore we found that even at low DNA concentration (0.9 μM), applying 450 μM of tetrazine results in very efficient labelling within 30 min. In comparison, 4 h are required for labelling by copper-catalyzed azide–alkyne cycloaddition in a similar setup when the same concentration of DNA albeit a 1900-fold excess of labelling reagent was used.9b
Next, we investigated if dvinATP can also be used in the polymerase chain reaction (PCR) by completely substituting natural dATP by dvinATP (Fig. 3). With the complete exchange of natural dATP by dvinATP, the full length product could be observed. The incorporation of 160 modified nucleotides into the DNA duplex was indicated by a change in the migration behavior of the DNA product, as monitored by gel electrophoresis analysis.
Still, the PCR product containing the vinyl groups undergoes DARinv when incubated with tetrazine for 1 h at room temperature, visible in a large shift of the band after addition of 1 (Fig. 3). As only one major band appeared after Diels–Alder reaction, one can conclude that a defined reaction product is formed, indicating that in most DNA strands a similar number of vinyl groups reacted with tetrazine. To address the efficiency of the DARinv using the PCR product, we digested the PCR product to the nucleosides and analyzed the products by HPLC. We found that the peak in the HPLC chromatogram corresponding to dvinA completely vanished and a new peak appeared at higher retention times (Fig. S4, ESI†) when the PCR product was incubated with tetrazine 1. These findings indicate that all vinyl groups reacted with tetrazine.
To summarize, here we show that the modified nucleoside triphosphate dvinATP is efficiently incorporated into DNA by a DNA polymerase. The modified biopolymer can undergo DARinv and can therefore be conjugated. We found that natural dATP can be substituted completely by its modified counterpart in PCR and still the full length product is formed, which can react in DARinv. All in all, we present an efficient tool for labelling and manipulation of enzymatically synthesized DNA.
We gratefully acknowledge funding by the DFG (SFB 969) and the Konstanz Research School Chemical Biology.
Footnote |
† Electronic supplementary information (ESI) available: Synthetic details of dvinATP and experimental details of kinetic measurements, PEX, PCR, labelling with tetrazine, and the protocol of the digestion of the PCR product to nucleosides. See DOI: 10.1039/c4cc04332d |
This journal is © The Royal Society of Chemistry 2014 |