## Introduction

Guanine-rich sequences of DNA can fold into tetra-stranded helical assemblies known as G-quadruplexes (G4s). These structures are implicated in a number of essential biological processes such as telomere maintenance, transcription, translation, and replication1,2,3,4. A series of bioinformatical studies initially suggested that there are over 350,000 putative G4-forming sequences in the human genome5,6, with subsequent studies reporting an even larger number7. Following these predictions, sequencing studies using purified human genomic DNA revealed over 700,000 sequences that form G4 structures under in vitro conditions8. More recently, the prevalence of G4s in human chromatin has been investigated using an immunoprecipitation technique9,10. These studies showed that there are over 10,000 sequences in the human genome that can form G4 DNA structures under cellular conditions9. Interestingly, these G4 structures are mainly located in gene promoter regions and in 5′-untranslated regions (5′-UTR) of genes supporting the proposed hypothesis that G4 DNA is involved in a number of essential biological regulatory processes.

While the exact roles that G4 structures play in biology are still under significant scrutiny, it is commonly accepted that G4 formation can be detrimental to certain biological processes and can lead to DNA damage11,12. Therefore, it is not surprising that several helicases such as Pif1, RecQ, RTEL1, FancJ, and BLM have been found to unfold G4 structures in vitro13. While it is known that G4 DNA helicases are important in maintaining genome integrity in cells, the direct link between their in vitro G4 unwinding activity and genome instability associated with their mutations is still missing.

Considering the wide range of biological processes associated with G4s, there has been significant interest in developing tools to detect and visualise G4 DNA structures in cells. With widespread application in immunofluorescent staining, high-affinity antibodies have been developed to visualise G4 in cells14,15,16,17,18,19. An early antibody found to be selective against telomeric G4 showed nuclear staining in the ciliate Stylonychia lemnae15. Subsequent studies have reported high-affinity antibodies able to visualise G4 DNA and G4 RNA in mammalian cells by immunofluorescent staining16,17,18. While these elegant studies are the most direct evidence of the presence of G4s in cells, they have some potential drawbacks. The fixation process can denature the cellular DNA and induce DNA degradation20,21, and the high affinity of the antibodies for G4 could artificially increase the presence of G4 structures. Furthermore, antibodies are not suitable for use in live cells and hence cannot be used to study G4 dynamics in real time.

These limitations can be overcome by using small-molecule optical probes22,23,24. Most G4 DNA optical probes reported to date rely on a large enhancement in emission intensity upon binding G4 (‘switch-on’), compared to binding duplex (ds) DNA24. For example, Thioflavin T (ThT) and its derivatives have shown to be switch-on probes for G4s, with up to 150-fold fluorescence enhancement vs. dsDNA (under optimal conditions) and have been used for live cell imaging of both DNA and RNA G4s25,26,27. However, ThT is known to bind to other biologically relevant molecules (e.g. protein aggregates28) and is highly sensitive to the matrix microviscosity29, potentially triggering non-G4 emission. While these small-molecule probes provide a good way of studying G4s in cell-free environments, their emission intensity is concentration dependent. In the vast excess of nuclear dsDNA (and other biomolecules), distinguishing G4 foci from background emission is challenging, even with a very high switch-on ability. Additionally, extracting quantitative information from emission intensity alone is difficult, since the cellular concentrations of neither the probe nor G4s are known. More complex approaches are required to gain insight in cellulo, such as the recently reported study using single-molecule fluorescence imaging for G4 detection30.

An alternative approach is to use a change in the fluorescence lifetime (a concentration-independent parameter) of a probe upon binding to different DNA structures31,32,33,34,35. For example, the fluorescence lifetime of 3,6-bis(1-methyl-2-vinyl-pyridinium) carbazole diiodide (o-BMVC) is longer when bound to G4 (ca. 2.5 ns) than non-G4 DNA sequences (ca. 1.5 ns). This difference was used to identify long lifetime foci in both the nucleus and cytoplasm of mammalian cells, however, this dye is only permeable to fixed cells and so no dynamic live cell work was possible33,34. More recently, a fluorescence lifetime-based probe (a tripodal cationic fluorescent molecule, NBTE) was reported that can distinguish G4 (3–4 ns) and dsDNA (2.0–2.5 ns) in live cells35. We previously reported that DAOTA-M2 [Fig. 1a] has a very different fluorescence lifetime when bound to G4 structures as compared to duplex or single-stranded DNA, with good live cell permeability and low cytotoxicity32. Herein we show that DAOTA-M2 can be used to visualise dynamic processes involving G4s in live cells. We confirm that while the probe works in fixed cells, there are differences in G4 abundance, highlighting the importance of carrying out G4 imaging experiments in live, rather than fixed environments. We demonstrate that DAOTA-M2 responds to the expression of DNA helicases FancJ and RTEL1 which are involved in genome stability and the distribution of G4 in live cells. Finally, we present a quantitative fluorescence lifetime-based assay to visualise the interaction of small molecules (which are not fluorescent themselves) with G4 structures in live cells.

## Results

### Biophysical characterisation of DAOTA-M2 interacting with DNA

Previously, we have shown that DAOTA-M2 is a medium-strength DNA binder36, with a moderately greater affinity for G4 over dsDNA (Kd = ca. 1.7 µM for dsDNA and ca. 1.0 µM for G4)32,37. Despite similar binding affinities, the intensity-weighted average lifetime (τw) upon binding is found to be dependent on the DNA topology. These values range from ca. 5–7 ns when bound to dsDNA, ca. 7–11 ns when bound to RNA and ca. 9–12 ns when bound to G4 DNA [Fig. 1b, c] and are independent of absolute concentration [Supplementary Fig. 1a]. Given the complex excited state decay of DAOTA-M2, we have now optimised our fitting algorithm and have chosen to use τw as a reporter instead of τ2 as used previously, due to a more straightforward and accurate fitting of fluorescence lifetime imaging data (vide infra)30.

To establish the effect of proteins, lipids, carbohydrates and biomolecules other than nucleic acids on the lifetime of DAOTA-M2, we used a highly protein-concentrated and nucleic acid-depleted Xenopus egg extract38. τw increases from 2.5 ± 0.3 ns in aqueous buffer to 7.3 ± 0.3 ns in cell extract [Fig. 1d], indicating an effect from other biomolecules on the fluorescence lifetime. Reassuringly, τw increases to 10.8 ± 0.6 ns on addition of G4 to the extract, and decreases to 6.1 ± 0.3 ns with dsDNA, consistent with the results observed in aqueous buffered solutions [Fig. 1c]. This result implies a higher affinity of DAOTA-M2 for DNA over other cellular biomolecules. In a nuclear environment, given the vast excess of nucleic acid, DAOTA-M2 should preferentially bind to DNA and the lifetime will give an indication of the DNA topology.

We next set out to examine whether the DAOTA-M2 lifetime can report on competitive interactions of other binders to G4 in vitro. Due to a higher affinity for quadruplexes, addition of G4 to a mixture of DAOTA-M2 and dsDNA increases the lifetime from 6.1 ± 0.2 ns [Fig. 1e, green trace] to 11.7 ± 0.4 ns [Fig. 1e, red trace]. The subsequent addition of pyridostatin (PDS), a selective G4 binder with a greater affinity for G4 than DAOTA-M2 (Kd = ca. 0.539,40 and ca. 1.0 µM32, respectively)41, displaces DAOTA-M2 from G4 back to dsDNA, accompanied by a drop in τw [Fig. 1f, black dots]. When the experiment is repeated using DAPI, which is a well-established dsDNA minor groove binder42 and non-G4 binder, only a small drop in τw is observed as DAOTA-M2 stays bound to G4 [Fig. 1f]. The dynamic equilibrium between dsDNA and G4 bound DAOTA-M2 can also be disrupted through the addition of a large excess of dsDNA into a solution of G4 and DAOTA-M2 [Supplementary Fig. 1b].

We then investigated DAOTA-M2 displacement using Ni-salphen, another DNA binder which has a higher affinity for both G4 and dsDNA than DAOTA-M2 [Supplementary Fig. 1c]43,44. In this case τw drops below the region associated with dsDNA to ca. 3.7 ns, close to that of free dye [Fig. 1f, orange dots]. A range of metal-salphen complexes (with metal = Ni, Cu, VO, Zn) are an ideal series to study structurally related molecules with different G4 affinities, as variation in the metal centre changes the metal coordination geometry, which has a dramatic effect on G4 binding: strong (Ni, Cu), medium (VO) and weak (Zn)45,46. Our DAOTA-M2 lifetime-based data [Fig. 1g] confirms a similar trend, with Ni, Cu and VO-salphen complexes displacing DAOTA-M2 more readily than Zn-salphen.

This data indicates that in mixtures of G4 and dsDNA, analysis of the DAOTA-M2 lifetime can accurately differentiate between distinct DNA topologies, thus, we next looked to investigate DAOTA-M2 in live cells using fluorescence lifetime imaging microscopy (FLIM).

### Imaging G4s in cellulo using DAOTA-M2 and FLIM

Given the in vitro assay results [Fig. 1] confirming that DAOTA-M2 lifetime can predict the strength of the interaction between small molecule binders and G4s, we set out to use DAOTA-M2 to study the interaction of any molecule with G4s in live cells. Incubation of U2OS cells with DAOTA-M2 (20 µM, 24 hr) results in nuclear staining [Fig. 2a], no obvious changes to cell morphology [Supplementary Fig. 4c], no increased DNA damage response [Supplementary Fig. 4a, b], and some accumulation of cells in S and G2 phases of the cell cycle [Supplementary Fig. 3a, b].

We then employed the same in vitro displacement assay [Fig. 1f] for in cellulo studies using PDS and DAPI. Co-incubation with DAOTA-M2 (20 µM) and PDS for 24 hr results in very different cellular lifetimes, dropping from 11.4 ± 1.0 ns in control cells to 10.3 ± 1.8 ns (5 µM PDS) and 9.0 ± 1.3 ns (10 µM PDS) [Fig. 3b]. The smaller drop in τw with a lower PDS concentration confirms the high concentration of PDS needed to disturb the equilibrium between DAOTA-M2 and G4, seen above in vitro [Fig. 1f]. As a negative control, incubation with DAPI (25, 50 and 90 µM, 1 hr) led to no change in the average nuclear lifetimes [Fig. 3b and Supplementary Fig. 6b], with nuclear localisation confirmed from the DAPI emission. Based on the consistency of these results with the in vitro characterisation [Fig. 1] and previous cellular work using DAOTA-M2 with PDS32, we propose that the lifetime drop in cellulo is the result of nuclear displacement of DAOTA-M2 from G4.

PDS (as well as many other G4 binders) is known to cause DNA damage, arrest cell growth and activate DNA damage response (DDR) pathways47. To establish whether the observed changes in DAOTA-M2’s fluorescence lifetime in cells could be due to PDS-dependent DNA damage rather than displacement of the probe from G4 structures, we carried out a control experiment with cisplatin. This compound is known to form DNA intra-strand links and activate the apoptotic pathway, but not to bind G4 DNA48. Encouragingly, co-incubation of cisplatin with DAOTA-M2 did not lead to a decrease in the fluorescence lifetimes recorded by FLIM [Supplementary Fig. 8a]. We also caused DNA damage by inducing double strand breaks with 2 Gy gamma irradiation. Irradiation of cells had no effect (p = 7.4 × 10−1) on the DAOTA-M2 lifetime [Fig. S8b], confirming that these two types of DNA damage were not the cause of the lifetime decrease observed after incubation of cells with PDS.

### FLIM studies using fixed cells

It is common for immunostaining or small molecule staining of G4 in cells to be performed following PFA fixation (needed for permeabilising the cellular membrane), which crosslinks proteins, increases cell rigidity and chemically alters the cell morphology. This process is known to impact nucleic acids within the cell, denaturing DNA and causing DNA damage20,21. However, DNAse and RNAse treatment is possible in fixed cells, and allows for examination of the effect of nuclear RNA on the DAOTA-M2 lifetime. This is an important control given the overlap in lifetimes when DAOTA-M2 is bound to G4 structures and non-G4 RNA [Fig. 1c].

Fixing with 4% PFA results in a drop in average τw by ca. 1 ns to 10.6 ± 1.1 ns, an interesting result as it implies changes in the number of G4s present upon fixation [Fig. 3d]. Reassuringly, addition of PDS (10 μM, 1 hr) has the same response as in live cells, with τw dropping to mean = 9.1 ± 1.4 ns and median = 8.5 ± 1.4 ns. In this experiment, the bi-modal distribution (formed due to limited PDS uptake by some cells) is best represented using the median. Treatment of fixed cells with RNAse (RNA digestion monitored using RNASelectTM, Supplementary Fig. 9) has no effect (p = 4.4 × 10−1) on the average τw, confirming that RNA in the cell nucleus does not affect DAOTA-M2 lifetime. DNAse treatment, however, did result in a drop in nuclear lifetime to 9.3 ± 0.9 ns. This value falls in-between that of DAOTA-M2 bound to dsDNA (median = 8.5 ± 1.4 ns) and in a mixture of dsDNA/G4 (10.6 ± 1.1 ns in fixed cells). This pattern is replicated in the Xenopus egg extract experiment described above [Fig. 1d].

Thus, our fixed cell experiments confirm that nuclear RNA does not contribute to the high DAOTA-M2 lifetime observed in fixed cells; this data gives us confidence that RNA is unlikely to interfere with live cell experiments. Therefore, the DAOTA-M2 lifetime can be attributed to G4 DNA structure formation. At the same time our data seem to indicate that more G4s are stained by DAOTA-M2 in live rather than in fixed cells (all of which are being equally displaced by PDS), although the effect of fixation on other cellular components and its knock-on effect on DAOTA-M2 binding cannot be excluded.

### Use of DAOTA-M2 to investigate helicases in live cells

We next investigated if DAOTA-M2 could report on the dynamics of G4 DNA inside live cells. We chose to disrupt the expression of the DNA helicases FancJ and RTEL1 [Fig. 4], which have been extensively reported, in vitro, to play a role in the resolution of G4s49,50,51, and monitor this using DAOTA-M2 in human and mouse cell lines. Cells lacking these proteins display general DNA replication stress, proposed to be the consequence of persisting G4s52,53. RTEL1 loss has been shown to cause sensitisation of mouse embryonic fibroblast (MEF) cells to G4 stabilising ligands, whilst FancJ loss did not – suggesting an increase in stable G4-DNA with the loss of RTEL1, but little or no increase with the loss of FancJ54.

To alter the general G4 content in cellulo, we used mutant MEF cells in which expression of the FancJ gene is eliminated, and the RTEL1 gene can be deleted using an adenovirus54. This allows for four combinations of MEF cells with FancJ and/or RTEL1 deletion to be studied: FancJ(+)/RTEL1(+), FancJ(+)/RTEL1(−), FancJ(−)/RTEL1(+), and FancJ(−)/RTEL1(−).

FancJ(+)/RTEL1(+) cells treated with DAOTA-M2 showed average nuclear lifetime of 7.7 ± 0.9 ns [Fig. S10c]. Lifetimes recorded in FancJ mutant MEF cells [FancJ(−)/RTEL1(+)] showed a modest, but significant (p = 6.6 × 10−3) increase in the mean lifetime [8.0 ± 1.0 ns, Supplementary Fig. 10c].

As studying RTEL1 requires cells to be infected, we studied both uninfected MEF cells and MEF cells infected with a null adenovirus. Given we saw the potential for small variations in DAOTA-M2 lifetime after infection [Supplementary Fig. 10c], the null infected samples were used as our basis for comparison for RTEL1 mutants [Fig. 4b]. Under these conditions, FancJ(+)/RTEL1(+) cells treated with DAOTA-M2 showed average nuclear lifetimes of 7.4 ± 0.8 ns [Fig. 4b]. A substantial effect (p = 1.1 × 10−14) was observed for the deletion of RTEL1 [FancJ(+)/RTEL1(−), 8.3 ± 0.9 ns, Fig. 4b]. A similarly significant effect (p = 4.5 × 10−9) was also seen for the deletion of RTEL1 in FancJ mutant cells, where the lifetime increased from 7.8 ± 1.0 ns [FancJ(−)/RTEL1(+), Fig. 4b] to 8.5 ± 0.9 ns [FancJ(−)/RTEL1(−), Fig. 4b]. There was no significant (p = 1.4 × 10−1) difference when comparing the single RTEL1 deletion [FancJ(+)/RTEL1(−)] to cells lacking both RTEL1 and FancJ [FancJ(−)/RTEL1(−), 8.5 ± 0.9 ns, Fig. 4b]. In the absence of FancJ and/or RTEL1, the longer DAOTA-M2 lifetimes suggest an increase in the stability and/or number of G4s. This is probably a direct effect and not a result of chromatin re-organisation since FancJ(+)/RTEL1(+) and FancJ(−)/RTEL1(+) show similar chromatin staining by DAOTA-M2 and DAPI [Supplementary Fig. 5c–e], which do not correlate with the observed DAOTA-M2 lifetime [Supplementary Fig. 5h].

FancJ and RTEL1 deficient MEF cells are known to present a DNA damage response54, therefore to control for DDR influence on DAOTA-M2 lifetime, MEF cells were exposed to 2 Gy gamma irradiation. ɣH2AX positive MEF cells did not show DAOTA-M2 lifetime variation compared to non-irradiated MEFs [Supplementary Fig. 8c]. Additionally, we noticed that DAOTA-M2 treatment on all four MEF cell lines induced an equivalent increase in ɣH2AX intensity [Supplementary Fig. 4d, e] and a moderate accumulation of cells in S and G2 phases of the cell cycle [Supplementary Fig. 3c, d], when compared to control MEFs treated with DMSO. Importantly, these phenotypes in the mutant MEF cell lines are similar to the one observed in WT MEFs and so are independent of the genotypes. Therefore, the recorded fluctuations in DAOTA-M2 lifetimes between mutant and WT MEF cells are indicative of an effect of the absence of the helicases FancJ and RTEL1 on G4 homoeostasis, and not on DNA damage or cell cycle.

To corroborate this finding, the human homologue of FancJ was studied in U2OS cells transfected with well-established FancJ siRNA50, 55,56,57,58 to achieve knock-down [98.6% efficient from the WB, Figure S10a], alongside control cells transfected with siRNA against luciferase [Fig. 4c]. Cells where FancJ expression was knocked-down showed significantly (p = 2.7 × 10−26) longer lifetimes [11.1 ± 0.7 ns], compared to control cells [10.5 ± 0.7 ns].

These results demonstrate the potential for DAOTA-M2 to be used directly to monitor the role of G4 DNA in live cells without affecting cells through fixation or co-incubation.

### In cellulo Fluorescence Lifetime Displacement Assay

G4s are considered as potential drug targets, and therefore it would be extremely useful to assess the ability of any given G4-targeted pharmaceutical to bind to this structure. Currently, a gold standard is to assess G4 DNA binders in vitro, with crucial information on whether they also target G4s in live cells missing. To add to our previous work using PDS as known G4 binder32, our next aim was to develop a FLIM based Fluorescence Lifetime Indicator Displacement Assay (FLIDA) to investigate a range of G4 binders on their ability to displace DAOTA-M2 from live cells. As our test dataset, we chose the Cu/Ni/VO/Zn-salphen complexes described in the in vitro studies (see above) since they are structurally related but have different G4 affinities [Fig. 1g]. All cell cultures incubated with potential G4 binders showed good viability alone (at 1 μM G4 binder over 24 hr) and in combination with DAOTA-M2 at the experimental conditions used for imaging [Supplementary Fig. 11].

In cellulo FLIDA using Ni-salphen resulted in a rapid drop in lifetime over 2 hr to 8.9 ± 0.7 ns, and after 6 hr the lifetime had reached 8.1 ± 0.6 ns [Fig. 5a, orange trace], consistent with PDS [Fig. 5a, black trace]. For Zn-salphen – which has been previously shown not to interact with G4s in vitro45 – no DAOTA-M2 displacement in live cells could be detected as the lifetime remains constant [Fig. 5a, grey trace]. Both Cu and VO-salphen complexes display intermediate behaviour with lifetimes that plateau at ca. 10 ns after 2 hr [Fig. 5a and Supplementary Fig. 12]. For Ni, VO and Zn-salphens, the in vitro trend [Fig. 1g] is replicated in cellulo [Fig. 5], correlating with the binding affinity of each complex for G443,44,45. Cu-salphen, a strong G4 binder, did not show the magnitude of lifetime change expected from in vitro data, a possible consequence of lower cellular or nuclear uptake. Thus, it appears that dynamic measurements enabled by FLIDA in live cells offer significant advantages in monitoring the ability of potential G4 binders to target G4 structures.

## Discussion

To establish the validity of the cellular FLIDA assays, we carried out experiments with a series of structurally related G4 binders (i.e. the metal-salphens, with M = Cu, Ni, VO, Zn). As indicated above, there is a clear structure-activity relationship between the in vitro binding affinities and the live cell FLIDA experiments. As a further negative control, we carried out FLIDA in live cells with DAPI, which localised in the nucleus (and bound to DNA) but did not change the nuclear τw of DAOTA-M2, consistent with DAPI not displacing the probe from G4 DNA.

Interestingly, cell fixation using PFA decreased the DAOTA-M2 lifetime which implies a difference in the nuclear distribution of G4 structures upon fixation (with a reduction in number of G4 sites available for binding with DAOTA-M2), a result that has not been observed previously. The FLIDA could be repeated in fixed cells using PDS, with displacement occurring to the same lifetime value as in live cells.

Having established how DAOTA-M2 interacts with G4 DNA using known G4 binders, we next designed experiments in which the nuclear G4 dynamics could be disturbed, without the need for co-incubation with strong G4 ligands. To achieve this, we reduced helicase enzyme expression in live cells through known protocols that knock-down FancJ in U2OS and knock-out FancJ and/or RTEL1, in MEF cells, respectively. Reducing the expression of known G4 helicases increases the number and/or stability of G4s, as the DAOTA-M2 lifetime increases. Studies using FancJ deficient human cells (U2OS and Hela) have reported that exposure to G4 ligands elicits a response in phenotypic markers (e.g. proliferation) when compared to wild type cells50, however, no such sensitivity was observed in FancJ deficient MEF cells54. We observe a modest lifetime increases when FancJ expression is reduced (0.5 and 0.3 ns, for U2OS and MEF cells, respectively). This increase is smaller than the decrease in lifetime after PDS displacement (ca. 2.5 ns), which is expected given that this helicase transiently targets specific regions of the genome and probably acts only on a proportion of the cellular G4 content inside each cell. Although the lifetime increase in MEF cells on loss of FancJ is small (0.3 ns), a larger effect is observed in MEF cells where RTEL1 has been deleted (0.6 ns). This is consistent with studies showing that RTEL1 loss led to sensitisation by G4-stabilising ligands, which was not observed with FANCJ loss. Taken together, these findings are in line with the suggestion that RTEL1 targets and resolves more efficiently genomic G4-forming sites than FancJ54.

We also noticed that MEF cells have a lower baseline average nuclear lifetime compared to U2OS (ca. 8 ns and ca. 11 ns, respectively). Embryonic MEF cells contain different euchromatin and heterochromatin organisation compared to U2OS cells61,62. While it is possible that the differences in chromosome packing between different cell lines have a direct effect on the lifetime of DAOTA-M2, we confirmed that high-intensity signal (indicating staining of chromatin) by DAOTA-M2 in the nucleus of both U2OS and MEF cells does not correlate with DAOTA-M2 lifetime (Supplementary Fig. 5). Additionally, as the PDS G4 displacement works in both live and fixed cells (Fig. 3), this lifetime change is unlikely to be only due to chromatin rearrangement.

Altering DNA helicase expression has multiple cellular and molecular effects on the genome, including transcriptome and RNA trafficking51,63,64, the possibility of forming ssDNA, double-strand breaks and affecting RNA molecules. Treatment of U2OS cells with cisplatin showed a slight increase in nuclear lifetime, indicating that intra-strand DNA adducts and inter-strand crosslinks can result in a shift in DAOTA-M2 lifetime (Supplementary Fig. 8a). However, dsDNA breaks induced by 2 Gy gamma irradiation had no effect on the DAOTA-M2 lifetime (Figures S8b, c). In all MEF cells used in this study, incubation with DAOTA-M2 resulted in the same DDR response as measured using ɣH2AX foci (Supplementary Fig. 4d, e). Given this result, it is very unlikely that the significant increase in lifetime measurements observed in the helicase mutant experiments reflects an increase in binding of DAOTA-M2 to other DNA structures that might form in these genetic backgrounds. With these factors relating to chromosomal packing and DNA damage accounted for, we can say with confidence that FLIM analysis of DAOTA-M2 reports directly on the prevalence of G4 structures in live mammalian cells.

G4 DNA targeting is emerging as a novel design strategy in the development of therapeutic drugs for diseases such as cancer65, thus, a robust method to test their G4 binding in live cells is highly desirable. We have demonstrated that DAOTA-M2 can be used to investigate G4 dynamics and their interaction with G4 binders in cellulo in real time. This approach holds promise for monitoring the sensitivity of newly developed G4 targeting drugs (e.g., testing against various cancer cell lines, including patient-derived samples) as well as for further understanding of the in vivo role of G4 DNA.

In summary, we have used DAOTA-M2 in combination with FLIM to monitor the formation of G4 DNA in the nuclei of live and fixed cells. We have developed a cellular assay to study the interaction of small molecules with G4 DNA, which can be applied to a wide range of drugs, which do not have intrinsic fluorescence. Our finding that cell fixation has a significant effect on the DAOTA-M2 lifetime, which must reflect a change in DNA topology, has wider implications for G4 studies that require fixations protocols. Additionally, our method can be used to study G4 DNA dynamics in live cells, for example when the expression of helicases known to unwind G4 in vitro is reduced or abolished. The knock-down of FancJ in U2OS or loss of FancJ and/or RTEL1 in MEF cells increase the nuclear lifetime, consistent with a reduction in amount of these enzymes. These experiments pave the way to directly study G4-related biological phenomena in live cells and to correlate the biological role of small molecules with their ability to target G4 DNA structures in live cells.

## Methods

DAOTA-M2 and metal-salphen (Ni, Cu, VO, Zn) complexes were synthesised as previously reported32,44,45. PDS was kindly donated by Dr. Marco Di Antonio, synthesised according to literature methods66,67. DAPI and cisplatin were purchased from commercial sources. Oligonucleotides (c-Myc and ds26; sequences = 5′-TGAGGGTGGGTAGGGTGGGTAA-3′ and 5′-CAATCGGATCGAATTCGATCCGATTG-3′, respectively) were purchased from Eurogentec, and dissolved in 10 mM lithium cacodylate buffer at pH 7.3. KCl was added to a final concentration of 100 mM, then the oligonucleotides were annealed at 95 °C for 5-10 min. Calf thymus DNA (CT-DNA, Sigma) was dissolved in the same cacodylate buffer, and KCl added to a final concentration of 100 mM. All oligonucleotide concentrations were determined unannealed using the molar extinction coefficients 13200 M−1 cm−1 (base pair for CT-DNA), 228700 M−1 cm−1 (strand for c-Myc), and 253200 M−1 cm−1 (strand for ds26). Concentrations of G4 and dsDNA are expressed as per strand, and per base pair, respectively.

### In vitro time-correlated single photon counting (TCSPC)

Time-resolved fluorescence decays were obtained using an IBH 5000 F time-correlated single-photon counting (TCSPC) device (Jobin Ybon, Horiba) equipped with a 467 nm NanoLED as an excitation source (pulse width < 200 ps, HORIBA) with a 100 ns time window and 4096 time bins. Decays were detected at λem = 575 nm (± 12 nm) after passing through a 530 nm long-pass filter to remove any scattered excitation pulse. For experiments using Ni-, Cu- or VO-salphens, a 404 nm NanoLED excitation source was used. For experiments involving ≤ 0.2 µM DAOTA-M2, 256 time bins were used detected at λem = 575 nm (±16 nm) to increase signal intensity per bin. Decays were accumulated to 10000 counts at the peak of fluorescence decay. A neutral density filter was used for the instrument response function (IRF) measurements using a Ludox solution, detecting the emission at the excitation wavelength. Data collection was performed using DataStation v2.2 (HORIBA Scientific) and analysed using DAS6 v6.8 (HORIBA Scientific). Traces were fitted by iterative reconvolution to the equation I(t) = I01et/τ1 + α2et/τ2) where α1 and α2 are variables normalised to unity. The intensity-weighted average lifetime (τw) was calculated using the equation:68

$$\tau _w = \frac{{\tau _1^2\alpha _1 + \tau _2^2\,\alpha _2}}{{\tau _1\,\alpha _1 + \tau _2\,\alpha _2}}$$
(1)

A prompt shift was included in the fitting to take into account differences in the emission wavelength between the IRF and measured decay. The goodness of fit was judged by consideration of the deviations from the model via a weighted residuals plot.

### In vitro fluorescence lifetime displacement assay

DAOTA-M2 (2 µM) was dissolved in 10 mM lithium cacodylate buffer (pH 7.3) supplemented with 100 mM KCl and the time-resolved fluorescence decay was recorded. If needed, dsDNA (CT-DNA, 20 µM) was mixed with DAOTA-M2 and the decay recorded. Pre-folded G4 DNA (c-Myc, 4 µM) was then added and the decay recorded. Increasing amounts of the corresponding molecules under study were added and the fluorescence decay recorded until no further changes were observed.

### In vitro fluorescence lifetime measurements with nucleic acid-depleted egg extracts

Decay data for nucleic acid-depleted cell extract studies was acquired by mixing 33 µL of nucleic acid-depleted Xenopus Laevis egg extracts38, with 12 µL of 10 mM lithium cacodylate buffer (pH 7.3) containing 100 mM KCl, DAOTA-M2 (final concentration 2 µM) and oligonucleotide (final concentration: c-Myc = 4 µM or ds26 = 44 µM). For samples where cell extract was not used, the same volume of 10 mM lithium cacodylate buffer (pH 7.3) containing 100 mM KCl was used in its place. Lifetimes decays were recorded using a home-built TCSPC method described previously69 with data collected using SPCM v9.83 (Becker & Hickl GmbH). Samples were excited using a pulsed diode laser (Becker & Hickl GmbH, 477 nm, 20 MHz) and emission collected at 575 nm (±15 nm), using a 550 nm long-pass filter to remove scattered excitation photons. Decay traces were fitted using the FLIMfit software tool developed at Imperial College London70 (v5.1.1, Sean Warren, Imperial College London) to a bi-exponential function, and the mean weighted lifetime (τw) calculated using Eq. (1).

### General cell culture

Human Bone Osteosarcoma Epithelial Cells (U2OS, from ATCC) were grown in high glucose Dulbecco’s modified Eagle medium (DMEM) containing 10% fetal bovine serum at 37 °C with 5% CO2 in humidified air.

### In cellulo fluorescence lifetime displacement assay

Cells were seeded on chambered coverglass (1.5 × 104 cells, 250 μl, 0.8 cm2) for 24 h, before washing with phosphate-buffered saline (PBS) and adding fresh media containing DAOTA-M2 (20 μM, 250 μl) for a further 24 h. For 24 hr co-incubation experiments, the compound under study was added with DAOTA-M2 and imaged 24 hr later. For < 24 hr co-incubation experiments, the compound udder study was added directly to the incubation media after 24 hr DAOTA-M2 incubation, and images were taken over time. Cells were imaged directly in the final incubation media. For time dependant measurements (Fig. 5), t = 0 cannot be measured directly as cells require equilibrating before imaging. Therefore, t = 0 was calculated from an average of all the control time points.

### Fixed Cell experiments

Cells were seeded on chambered coverglass (1.5 × 104 cells, 250 μl, 0.8 cm2) for 24 h, before washing with PBS and adding fresh media containing DAOTA-M2 (20 μM, 250 μl) for a further 24 h. Cells were washed (x3) in ice-cold PBS before incubation in ice-cold paraformaldehyde (PFA, 4% in PBS) solution for 10 min, and a further wash (x3) with ice-cold PBS. Fixed cells were further treated with PDS (10 μM, 1 h, 21 °C), RNAse A (1 mg ml−1, 10 min, 21 °C, Merck) or DNAse (200 Units well−1, 1 hr, 37 °C, Qiagen). DAPI was stained at 0.5 µM (5 min) and RNASecelctTM at 0.5 µM (20 min) in PBS. To minimise the impact of fixation on the DAOTA-M2 lifetime due to the refractive index of the media59, all FLIM experiments on fixed cells were performed without fixative, under a solution of PBS.

### Cell culture for helicase knock-down and knock-out experiments

For FancJ helicase knock-down treatment, a solution of 30 nM siRNA (SigmaAldrich, 5′- GUACAGUACCCCACCUUAU -3′) and DharmaFECT reagent (used as per manufacturer’s instructions, Dharmacon) in serum-free DMEM was prepared and incubated at RT for 30 min. 400 µL of this solution was mixed with 2.1 mL DMEM containing 10% FBS and used to seed cells (1.6 × 105 cells, 2.50 ml, 9.6 cm2) for 16 hr at 37 °C. The growth medium was replenished, and cells further incubated for 24 h before reseeding on chambered coverglass (5.0 × 104 cells, 400 μl, 0.8 cm2) with the addition of DAOTA-M2 (10 µM) for a further 24 hr before imaging. Cells treated analogously using an siRNA for Luciferase (Dharmacon, 5′- UCGAAGUAUUCCGCGUACG -3′) were used as a control. The knockdown efficiency was assessed by Western blot for FancJ compared to actin [Figure S10a].

Mutant mouse embryonic fibroblast (MEF) cells were used in which the FancJ gene is compromised by a gene trap cassette, eliminating expression of the FancJ ORF, resulting in a null allele43. In these cells the RTEL1 gene is flanked by lox P sites, allowing RTEL1 deletion by infection with adenovirus harbouring the CRE recombinase protein. RTEL1F/F FancJ+/− and RTEL1F/F FancJ−/− MEF cells (a kind gift from S. Boulton) were cultured as described above for U2OS cells. For studies of RTEL1 knock-out, cells were left without infection, or cells were incubated with 30 MOI of either Null or CRE adenovirus (Vector biolabs) with 1x polybrene and 2% FBS in serum-free DMEM for 2 hr at 37 °C with shaking, before returning to culture. This infection was repeated after 48 hr. Cells were grown for a further 72 hr before preparation for FLIM.

For FLIM, cells were reseeded on chambered coverglass (1.5–5 × 104 cells, 200 μl, 0.8 cm2) for 24–48 h in media, incubated with DAOTA-M2 (20 μM) for 24 h before imaging.

### MTS cytoxicity assay

U2OS cells were seeded (5 × 103 cells, 100 μl, 32.2 mm2) in a 96-well plate. After 24 h, compounds under study were added at the appropriate concentration in triplicate (150 μl). After a further 24 h, the MTS/PMS reagents were added according to the Promega MTS Assay protocol. The average absorbance of the triplicate wells was recorded at 492 nm, and where applicable, readings were corrected for compound absorbance by subtracting the compound-only control run in parallel. Wells were maintained with DMSO (only cells) as 100% and the maximum compound concentration as 0% viability. For experiments involving co-incubation with DAOTA-M2, cells with only DAOTA-M2 incubation were used as 100% and no cells as 0%. Absolute IC50 was determined from the dose-response curve of absorbance vs. logarithm of concentration of compound.

### Fluorescence imaging

DAPI emission (400–450 nm) was collected following multi-photon excitation at 760 nm with 665 and 680 nm cut off filters. RNASelectTM emission (495–545 nm) was collected following 488 nm excitation. When RNASelect was present, DAOTA-M2 emission (570–700 nm) was collected following 561 nm excitation. Software for confocal imaging and analysis was LAS AF v.2.6.0 (Leica).

### Fluorescence lifetime imaging microscopy (FLIM)

FLIM was performed through time-correlated single-photon counting (TCSPC), using an inverted confocal laser scanning microscope (Leica, SP5 II) and a SPC-830 single-photon counting card (Becker & Hickl GmbH). A pulsed diode laser (Becker & Hickl GmbH, 477 nm, 20 MHz) was used as the excitation source, with a PMC-100-1 photomultiplier tube (Hamamatsu) detector. Software for collecting FLIM images was SPCM v9.83 (Becker & Hickl GmbH). Fluorescence emission (550–700 nm) was collected through a 200 μm pinhole for an acquisition time sufficient to obtain signal strength suitable for decay fitting, or a maximum of 1000 s. For all live-cell imaging, cells were mounted (on chambered coverglass slides) in the microscope stage, heated by a thermostat (Lauda GmbH, E200) to 37 (±0.5) °C, and kept under an atmosphere of 5% CO2 in air. A 100x (oil, NA = 1.4) or 63x (water, NA = 1.2) objective was used to collect images at either 256 × 256 pixel resolution or at 512 × 512 pixel resolution, as stated in the text. The IRF used for deconvolution was recorded using reflection of the excitation beam from a glass cover slide.

Lifetime data were fitted using the FLIMfit software tool developed at Imperial College London (v5.1.1, Sean Warren, Imperial College London)70 to a bi-exponential function, and the mean weighted lifetime (τw) calculated using Eq. (1). 7 × 7 and 9 × 9 square binning was used to increase signal strength for images recorded at 256 × 256 and 512 × 512 resolution, respectively. A scatter parameter was added to the decay fitting to account for scattered excitation light. Before fitting, a mask was applied to the images to analyse individual cell nuclei. Fitted lifetime data for each pixel within a single cell nucleus were pooled to find average and median nuclear τw values. A threshold was applied to the average of each nucleus to require a minimum of 300 at the peak of the decay and a goodness-of-fit measured by χ2 of less than 2. Average nuclear intensity in FLIM images was calculated from the peak maximum of the fitted decay (excluding scatter), averaged across the nucleus.

Chamber slides containing either U2OS or MEF cells were inserted into the Irradiator (GSR D1 Cell Irradiator) for 50 s to irradiate cells to 2 Gy. Control cells were left outside for the equivalent time. Samples for FLIM were then imaged as above, except MEF cells which were imaged using a 20x (NA = 0.7) objective. To confirm DNA damage, slides were further incubated for 30 min to allow initiation of damage repair by the cells, then imaged for ɣH2AX immunofluorescence staining.

### ɣH2AX staining

Cells were permeabilised with Triton X-100 buffer (0.5% Triton X-100; 20 mM Tris pH 8; 50 mM NaCl; 3 mM MgCl2; 300 mM sucrose) at RT for 5 min and then fixed in 3% formaldehyde/2% sucrose in PBS for 15 min at RT and washed with PBS (x3). After a 10 min permeabilisation step and a wash in PBS, nuclei were incubated with blocking solution (10% goat serum in PBS) for 30 min at 37 °C and stained with mouse-anti-γH2AX (1/500, Millipore 05–636) for 1 h at 37 °C followed by O/N incubation at 4 °C. After washing in PBS (x3), slides were incubated with secondary goat anti-mouse Alexa 488 antibody (1/400, Life Technologies A11001) for 40 min at 37 °C, washed in PBS (x3), and incubated with ethanol series (70, 80, 90, 100%). Slides were mounted with antifade reagent (ProLong Gold, Invitrogen) containing DAPI, and images were captured with Zeiss microscope using Carl Zeiss software.

### Fluorescence-activated cell sorting (FACS)

Cells in culture were treated with BrdU (10 µM) in medium for 30 min before collection with trypsin and resuspended in PBS (300 µL). Ice-cold methanol (700 µL) was added dropwise with mixing and the samples were stored at −20 °C for a minimum of 2 h. Fixed cells were harvested by centrifugation and incubated with pepsin (2 mL, 0.2 mg/mL in 2 M HCl, RT) for 20 min. Samples were washed with PBS and resuspended in 0.5 m: block solution (PBS, 0.5% Tween20, 0.5% BSA) with αBrdU-FITC conjugate (20 µL) for 1 h at RT. Samples were washed with the same solution then resuspended in PBS containing RNaseA (0.5 mg/mL, 1 mL, 37 °C, 15 min). Propidium iodide (10 µg/mL) was added for 5 min at RT and samples were stored at 4 °C for FACS. Data and graphs were analysed and generated using FlowJo software (BD biosciences), using Watson (Pragmatic) module.

### Western Blot

Protein was extracted from cells using a lysis buffer (40 mM NaCl, 25 mM Tris pH 8, 2 mM MgCl2, 0.05% SDS, 2x Complete EDTA-free protease inhibitor (Roche), 0.4 µL mL−1 benzonase) with protein concentration determined by Bradford assay, comparing to BSA standards to ensure loading of an equal mass of protein into each lane. Protein and Laemmli buffer were heated to 100 °C for 5 min before loading into gel. For U2OS, NuPAGE Novex 4–12% Bis-Tris Gel (Invitrogen) was used. For MEFs, NuPAGE Novex 3–8% Tris-Acetate Gel (Invitrogen) was used. Samples were run on gels for 2 hr before transfer from gel to a nitrocellulose membrane. Antibodies used to bind proteins on membrane were pAb rabbit BRIP1/FANCJ antibody (1/10000, Novus Biologicals NBP1-31883), pAb rabbit RTEL1 antibody (1/5000, Novus Biologicals NBP2-22360). For loading control, mAb mouse anti-β-actin antibody (1/5000, Abcam ab8226) was used with U2OS and mAb mouse anti-α-Tubulin (1/10000, Sigma Aldrich T6199) was used with MEFs. Secondary antibodies used were: pAb swine anti-rabbit immunoglobulins/HRP (1/10000, Dako P0217) and pAb goat anti-mouse immunoglobulins/HRP (1/5000, invitrogen A16078). Visualisation was performed by exposure onto photographic film for U2OS and visualisation using Amersham ImageQuant 800 for MEFs. Full uncropped scans are available in the source data file.

### Statistics

Results are expressed as mean ± SD (unless stated otherwise). Two-tailed non-paired t-tests were performed using OriginPro v9.55. p-values, t-values, and degrees of freedom (DF) are stated in the figure captions. Significance: ns p > 0.05, *p < 0.05, **p < 0.01, ***p < 0.001. n values are the total cell nuclei that meet the threshold requirements. For box plots, the box represents 25–75% range, error bars are the mean ± SD, horizontal line is the median and the grey dot is the mean.

### Reporting Summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.