Single Molecule Analysis of Laser Localized Psoralen Adducts

Summary

Lasers are frequently used in studies of the cellular response to DNA damage. However, they generate lesions whose spacing, frequency, and collisions with replication forks are rarely characterized. Here, we describe an approach that enables the determination of these parameters with laser localized interstrand crosslinks.

Abstract

The DNA Damage Response (DDR) has been extensively characterized in studies of double strand breaks (DSBs) induced by laser micro beam irradiation in live cells. The DDR to helix distorting covalent DNA modifications, including interstrand DNA crosslinks (ICLs), is not as well defined. We have studied the DDR stimulated by ICLs, localized by laser photoactivation of immunotagged psoralens, in the nuclei of live cells. In order to address fundamental questions about adduct distribution and replication fork encounters, we combined laser localization with two other technologies. DNA fibers are often used to display the progress of replication forks by immunofluorescence of nucleoside analogues incorporated during short pulses. Immunoquantum dots have been widely employed for single molecule imaging. In the new approach, DNA fibers from cells carrying laser localized ICLs are spread onto microscope slides. The tagged ICLs are displayed with immunoquantum dots and the inter-lesion distances determined. Replication fork collisions with ICLs can be visualized and different encounter patterns identified and quantitated.

Introduction

DNA is under constant assault from exogenous agents such as radiation, ultraviolet light, environmental toxins, combustion products, etc. Additionally, it is also attacked by endogenous radical species produced by oxidative metabolism. All of these have the potential to chemically or physically disrupt the integrity of DNA ¹. Perturbations in the genome can activate the DNA Damage Response (DDR), a recruitment and post translational modification cascade with hundreds, if not thousands, of proteins and microRNAs involved in lesion repair, regulation of the cell cycle, apoptosis, senescence, and inflammatory pathways ².

Most of our information about the DDR comes from studies with DSBs. This is in large part due to the availability of technologies for introducing breaks, including sequence specific breaks, in genomic DNA in living cells ³. In addition, the propensity of breaks to induce foci of DDR proteins, which can be displayed by immunofluorescence, has been very helpful for identifying the kinetics and requirements of responding proteins. One of the key technologies for studying the DDR was introduced by Bonner and colleagues, who used a laser beam to direct a stripe of DSBs in a "Region of Interest" (ROI) in the nuclei of living cells ⁴. In effect, they created a lengthy focus in which proteins of the DDR could be identified by immunofluorescence. This was illustrated by their demonstration of the strong stripe of phosphorylated histone H2AX (γ-H2AX) in the laser exposed cells. Since then, the laser approach has been employed in numerous studies of the DDR induced by DSBs. Although powerful and popular, and the source of dramatic immunofluorescence images, it should be noted that in most experiments the laser intensity is adjusted so as to produce observable results, without concern for lesion identity, density, or spacing. Indeed, it can be difficult to make these estimates. Thus they are largely ignored, despite the multiplicity of lesions introduced into DNA by lasers ⁵. This contributes to the many contradictions in the literature ⁶.

In contrast to DSBs, most chemical modifications of DNA do not stimulate the formation of discrete foci of DDR proteins. This is important in the light of our current understanding of lesion frequencies. It has been estimated that human cells in culture incur as many as 50 DSBs per cell cycle, formed largely during S phase ^7,8,9. Fewer are formed in non-proliferating cells. This contrasts with the number of nucleobase losses or modification events, which are in the tens of thousands per cell/day ^1,10. Thus, we know most about the DDR induced by events that are relatively rare, and much less about those induced by helix distorting lesions, which in aggregate are far more common.

In order to address questions about the cellular response to covalent modifications of genomic DNA, we wanted to work with a helix distorting DNA adduct that had inherent DDR induction activity. Furthermore, to facilitate experimental design and interpretation we were interested in a structure whose introduction could be controlled with respect to time and was amenable to visualization. Accordingly, we developed a strategy based on psoralen. Psoralens are well characterized photoactive DNA intercalators favoring 5' TA:AT sites. Unlike other crosslinking agents such as nitrogen mustards and mitomycin C (MMC) they are not DNA reactive unless exposed to long wave UV (UVA) light. The intercalated molecules react with thymine bases on opposite strands to produce helix distorting interstrand crosslinks (ICLs) ¹¹. With the trimethyl psoralen used in our experiments most products are ICLs, relatively few monoadducts are generated (less than 10%) ¹², and intrastrand crosslinks between adjacent bases on one strand are not formed. Because they are powerful blocks to replication and transcription, psoralen and other crosslinking agents, like cis-platinum and MMC, are commonly used in chemotherapy. Thus psoralen enabled studies that followed the activation of the DDR by a helix distorting structure, and also provided insight into the cellular response to a compound with clinical importance.

We synthesized a reagent in which trimethyl psoralen was linked to digoxigenin (Dig), a plant sterol not found in mammalian cells and frequently used as an immunotag. The requirement for photoactivation permits localization by laser light (365 nm) of psoralen ICLs in defined ROI in nuclei in living cells. These can be displayed by immunofluorescence against the Dig tag. DNA repair and DDR proteins appeared in the stripes of laser localized ICLs ^13,14.

The DDR activated by the high laser intensities used to produce DSBs could be due to isolated or clustered damage ^15,16. Consequently, the relevance of results from these experiments to naturally occurring lesions, present at much lower concentration, is uncertain. To address similar questions about psoralen adduct frequency and spacing in DNA, we took advantage of DNA fiber technology ¹⁷ and immunoquantum dots. Quantum dots are much brighter than fluorescent dyes and are not bleached by exposure to light. Thus they are frequently used for single molecule imaging ¹⁸, an application for which fluorescent dyes are insufficiently bright. Individual DNA fibers can be stretched on glass slides and can be displayed by immunofluorescence against nucleoside analogues incorporated during incubations prior to cell harvest. We treated cells with Dig-psoralen and exposed the ROI to laser micro irradiation. Fibers were prepared from the cells and individual Dig-psoralen adducts could be visualized with the immunoquantum dots. Exposing the cells to nucleoside analogues for relatively short times (20-60 min) permits the display of replication tracts in the vicinity of the laser localized ICLs.

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Protocol

1. Preparation of Dig-TMP

1. Mix 50 mg (0.18 mmoles) of 4'-chloromethyl-4,5',8-trimethylpsoralen and 590 mg (2.7 mmoles) of 4,7,10-trioxa-1,13-tridecanedi-amine in a dry 25 mL round-bottom flask under nitrogen. Add 10 mL toluene and reflux for 12 h. Remove solvent in a rotary evaporator under reduced pressure.
   1. Purify the residue by flash column chromatography over silica gel. Elute the column with chloroform, methanol, and 28% ammonia solution (9:1:0.5). Evaporate the solvent in a rotary evaporator under reduced pressure, and recover the pure 4'-[N-(13-amino-4,7,10-trioxatrideca)]aminomethyl-4,5',8-trimethylpsoralen as a pale yellow viscous liquid.
   2. Mix 5.5 mg (0.012 mmoles) of 4'-[N-(13-amino-4,7,10-trioxatrideca)]aminomethyl-4,5',8-trimethylpsoralen with 5 mg (0.008 mmoles) of digoxigenin NHS ester in a dry round-bottom flask under nitrogen. Add 0.5 mL anhydrous dimethyl formamide (DMF) and 3.4 µL of trimethylamine and stir at 50 °C for 18 h.
   3. Remove solvent in a rotary evaporator under reduced pressure.
   4. Dissolve the residue in minimum amount of dichloromethane. Apply the solution in 2 µL spots horizontally across the bottom of a preparative thin layer plate with silica gel as a stationary phase. Run the preparative TLC in chloroform: methanol: 28% ammonium hydroxide (8:1:0.1).
   5. Mask the plate except for the vertical edges and identify the band of product with short wavelength UV 254 nm lamp. Scrape the product from the plate with a spatula and isolate the pure product using chloroform: methanol: 28% ammonium hydroxide (8:1:0.1) mixture.
   6. Remove solvents in a rotary evaporator under reduced pressure. Dissolve the residual pellets in 1 mL of 50% EtOH:H₂O, dispense into 50 µL aliquots in 1.5 mL tubes (~20 aliquots) and dry in a centrifugal evaporator until all solvent is evaporated (~3 h).
   7. Redissolve each aliquot in 200 µL of 50% EtOH:H₂O and dry again in a centrifugal evaporator. Dissolve each aliquot again in 200 µL of 50% EtOH:H₂O, dry in a centrifugal evaporator and store pellets at -20 °C for long term storage.
2. For use, dissolve the pellet in 50 µL of 50% EtOH:H₂O. Prepare a 1:100 dilution of the dissolved Dig-TMP in H₂O and measure OD at 250 nm. The extinction coefficient of Dig-TMP is 25,000. The solution is stable for about a month if stored at -20 °C. Verify the concentration by measuring OD at 250 nm before each use.
   1. Calculate stock concentration: Abs x 100 x10⁶/25,000 = Concentration (in µM). Typically the stock solution is about 3 mM. It is important to be in this range in order to minimize the volume of EtOH added to the medium.

2. Laser Localized Dig-TMP ICLs

1. Perform laser localization with a confocal microscope with a SRS nitrogen laser (337 nm) pumped through a dye cell emitting a line of 365 nm and firing 3 ns pulses at 10 Hz, with a power of 0.7 nW.
2. Make a vertical mark on the side of a 35 mm glass bottomed cell culture dish with a marking pen. Scratch a cross in the center of the glass on the culture surface with a diamond pen such that the black stripe on the side of the dish is at the top of one arm of the cross. The cross is marked on the growth surface of the glass so that it and the cells will be in the same focal plane.
3. Sterilize the plate after marking with a rinse of 70% EtOH. Dry before plating cells.
4. Plate cells (standard laboratory strains such as HeLa or U2OS) in the cross marked culture dishes one or two days before. Cell should be actively dividing and 50-70% confluent on the day of the experiment. Incubate 24 h with 1 µM 5-chloro-2-deoxyuridine (CldU) to uniformly label DNA.
5. Add Dig-TMP in 50% EtOH: H₂O to cell culture medium to a final concentration of 20 µM. Bring the medium to 37 °C. Change the medium over the cells and place in incubator (37 °C, 5% CO₂) for 30 min to allow the Dig-TMP to equilibrate.
6. While the cells are incubating, establish the x/y coordinates of the field of view in which the laser is active. Follow the manufacturer's calibration procedure in which the laser is directed by the software to etch a mirrored glass slide along a horizontal and diagonal line. The two lines define the boundaries of the field in which the laser can strike a target.
7. Place the plate in the environmental chamber, at 37 °C with controlled CO₂ and humidity, on the microscope stage and focus with the 60X oil objective on the intersection of the cross.
8. Direct the 365 nm laser beam to an ROI, established by the investigator with the shape tool in the software, to form a stripe of 3 µm x 0.6 µm. The outline of the ROI is placed by the cursor in nuclei of cells located in the immediate vicinity of the intersection of the cross. Adjust the z focal plane to target the laser midway through the nucleus. Use a laser in the range of 350-370 nm. 405 nm lasers cannot induce crosslinks ¹⁹.
   NOTE: We locate the ROI in nucleoplasmic areas outside the nucleoli, which can be distinguished from nucleoplasm in differential interference contrast (DIC) imaging.
9. Verify the focus and activity of the laser by increasing the power setting to a level sufficient to obliterate a cell (the cell will darken and then disappear). This is an important diagnostic for an unimpeded light path for the laser through the microscope and then through the coverslip and into the cells.
   1. Lower the power setting to just enough to activate the psoralen and the ICL induced DDR (this must be determined empirically for each laser/microscope combination). Use a laser intensity setting (1.7% here) that does not activate the DDR in the absence of psoralen (monitored by the formation of γ-H2AX).
      NOTE: This is an important determination and the settings may require adjustment if the laser source or a component in the light path is changed. Follow the accumulation of GFP tagged repair proteins such as XPC or FAN1, both of which are rapidly recruited (in seconds) to the laser psoralen stripes, but not to ROI exposed to the laser alone. Some proteins of the DDR appear within seconds, while several minutes may be required for others. It is necessary to perform time course determinations for each protein of interest. We also note that in cells that were not exposed to the laser there are no stripes of responding proteins.
10. After all cells in a field have been targeted move the plate to a new field, staying close to the intersection of the cross.
11. In experiments designed to determine the distribution of inter lesion distances expose cells to the laser in 20-25 fields (4-5 cells/field) around the intersection. In order to analyze replication patterns in the vicinity of the localized ICLs incubate cells with 10 µM 5-Iodo-2-deoxyuridine (IdU) after laser firing.
    NOTE: The time of incubation with IdU is somewhat arbitrary. We have used as short as 20 min and as long as 60 min (see below). Longer pulses (a few hours) often result in multiple replication tracts coalescing, thus losing the opportunity to image the progress of single forks. In some experiments ces are labeled with CldU for 24 h to uniformly label DNA prior to exposure to Dig-TMP followed by pulse labeling of replication tracts.

3. Harvest of Cells and Stretching of DNA Fibers

1. Remove the plate from the stage, remove the medium, and wash with phosphate buffered saline (PBS). Remove the PBS solution. Place a 10 µL drop of a commercial trypsin/EDTA solution on the intersection of the cross in the middle of the glass surface.
2. Incubate for 3-4 min at room temperature (RT) and then draw the trypsin solution with the detached cells into the pipet tip. There is no need to neutralize the trypsin.
3. Place the drop of trypsin/EDTA with the cells at one end of a silanized glass microscope slide. Lyse the cells and release the DNA by addition of 10 µL of 0.5% SDS solution and incubate for 3-4 min at RT mixing gently with the pipet tip, allowing the periphery of the pool to dry.
4. Tilt the slide 20º and allow the liquid to run down to the end. The DNA fibers are extended/stretched by the hydrodynamic forces of the flowing liquid. Let the slides air dry (~10 min) and fix in 3:1 methanol/acetic acid for 10 min. Remove the slides from the fix solution and air dry again. At this point they can be stored indefinitely in 70% EtOH at -20 °C. On removal from the 70 % EtOH allow to air dry before the next step.
5. Wash slides in PBS, and then denature in 2.5 M HCl for 1 h at RT. This treatment depurinates DNA making the incorporated halogenated nucleobases accessible to antibodies.
6. Neutralize slides in 0.4 M Tris-HCl, pH 7.4. Wash twice in PBS/0.5% Tween-20 (PBST) for 5 min each.
7. Block slides with 5% bovine serum albumin (BSA) and 10% goat serum in PBS. Cover the slides gently with a parafilm to spread the blocking solution evenly over the slide and incubate for 1 h at RT.
8. Pipet 100 µL of 1:200 dilution in blocking solution of rat anti-bromodeoxyuridine (specifically detects CldU) primary antibody to each slide. Cover the slides gently with a parafilm to spread the dilution evenly over the slide and incubate in a humidified chamber for 1 h at RT. Remove the parafilm and wash the slides three times in PBST for 5 min each.
9. Pipet 100 µL of diluted (1:100) goat anti-rat Alexa Fluor 647 in blocking solution to each slide. Cover the slides gently with a parafilm and incubate for 45 min at RT. Wash the slides three times in PBST for 5 min each.
10. Pipet 100 µL of diluted (1:40) mouse anti-bromodeoxyuridine (detects ldU and CldU. This dual specificity necessitates the blocking of CldU by the rat anti BrdU in the prior incubation) primary antibody and rabbit anti-DIG antibody (1:200) in blocking solution to each slide. Cover the slides gently with a parafilm and incubate in a humidified chamber for 1 h at RT. Wash the slides three times in PBST for 5 min each.
11. Pipet 100 µL of diluted (1:100) goat anti-mouse Alexa Fluor 488 andc(1:5,000) goat anti-rabbit probe (e.g., Qdot 655) in blocking solution to each slide. Cover the slides gently with parafilm and incubate for 45 min at RT. Wash the slides three times in PBST for 5 min each.
12. Drain excess PBST onto a paper towel. Add 50 µL of antifade mounting medium onto each slide and cover with a coverslip. Image or store for no more than 48 h at -20 °C.

4. Fiber Imaging by Fluorescence Microscopy

1. Perform image acquisition through a 63X objective on an inverted microscope with an attached fully motorized filter wheel with FITC, Cy5 and Q Dot 655 detection. The excitation filter is 425 nm, and the emission filter is 655 nm with 20 nm centered at the emission peak ²⁰.

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Results

Laser localized Dig-TMP (Figure 1A) ICLs can be displayed by immunofluorescence against the Dig-tag linked to the psoralen. Although the laser can be directed to strike in an area of any contour, stripes are not "natural" shapes in cells, and legitimate signals can be easily distinguished from artifacts due to non-specific binding by primary or secondary antibodies. This feature is helpful when using antibodies of less than perfect specificity. An example of the w...

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Discussion

The laser localization technology requires the use of adherent cells with nuclei that are visible in bright field microscopy. We have tried to attach nonadherent cells, such as primary lymphocytes, or loosely adherent cultured cells such as AD293, to the glass surface with cell adhesive preparations such as polylysine or collagen, or more complex mixtures. Although these treatments may bind the cells to the surface, we find that they generally stay rounded making it very difficult to focus into the nuclei. Furthermore, t...

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Materials

Name	Company	Catalog Number	Comments
Digoxigenin NHS ester	Sigma-Aldrich	11333054001
Chloro-psoralen	Berry and Associates	PS 5000
diaminoglycol	Sigma-Aldrich	369519	4,7,10-Trioxa-1,13-tridecanediamine
Chloroform	Acros Organics	423550040
Methanol	Fisher Scientific	A4524
Ammonium solution	Sigma-Aldrich	5002
TLC plates	Analtech, Inc.	P02511
Flass glass column 24/40, 100 mL	Chemglass Life Sciences	CG-1196-02
Nikon T2000_E2 spinning disk confocal microscope, equipped with automated stage and environmental control chamber and plate holder	Perkin Elmer		With Volocity Software
Micropoint Galvo	Andor Technologies		with a Nitrogen pulsed laser
dye cell	Andor Technologies	MP-2250-2-365
365 dye	Andor Technologies	MP-27-365-DYE
IdU	Sigma-Aldrich	17125
35 mm glass botomm plates 1.5 coverslip, 10 mm glass diameter, uncoated	Matek	P35G-1.5-10-C
microscope slides	New Comer Supply	Part # 5070	New Silane Slides
Mouse anti BrdU antibody (IdU)	BD Biosciences	347580	1 in 40
Rat anti BrdU Antibody (CldU)	Abcam	ab6326	1 in 200
Rabbit anti Dig antibody	ThermoFisher Scientific	710019	1 in 200
Q-dot 655 goat anti Rabbit IgG	ThermoFisher Scientific	Q-11421MP	1 in 5,000
AF647- goat anti Rat IgG	Jackson Immunoresearch	112-605-167	1 in 100
AF488-goat anti mouse IgG	Jackson Immunoresearch	115-545-166	1 in 100
Zeiss epifluorescent microscope A200	Zeiss		with Axiovision software
Q-dot 655 filter	Chroma	39107