By enlarging the aperture along the optic axis, the coherent utilization of opposing objective lenses (4Pi arrangement) has the potential to offer the sharpest and most light-efficient point-spread-functions in three-dimensional (3D) far-field fluorescence nanoscopy. However, to obtain unambiguous images, the signal has to be discriminated against contributions from lobes above and below the focal plane, which has tentatively limited 4Pi arrangements to imaging samples with controllable optical conditions. Here we apply the 4Pi scheme to RESOLFT nanoscopy using two-photon absorption for the on-switching of fluorescent proteins. We show that in this combination, the lobes are so low that low-light level, 3D nanoscale imaging of living cells becomes possible. Our method thus offers robust access to densely packed, axially extended cellular regions that have been notoriously difficult to super-resolve. Our approach also entails a fluorescence read-out scheme that translates molecular sensitivity to local off-switching rates into improved signal-to-noise ratio and resolution.
The three to seven fold improved axial resolution provided by 4Pi microscopy1,2,3 in the 1990s marked a first step in the quest for radically improving the resolution in far-field fluorescence microscopy. Yet the resolution provided by 4Pi microscopy remained diffraction-limited, because by jointly using two opposing lenses for focusing the excitation and/or the fluorescence light, this method just optimized the focusing conditions for feature separation. Modern far-field fluorescence nanoscopy4, or superresolution microscopy, such as the methods called stimulated emission depletion (STED), reversible fluorescent saturable optical transition (RESOLFT) and later also photoactivated localization microscopy (PALM)/stochastical optical reconstruction microscopy (STORM) fundamentally departed from such early superresolution concepts by discerning features through a molecular state transition. The use of a state transition for feature separation, typically a transition between a fluorescent (ON) and a non-fluorescent (OFF) state, opened the road to lens-based fluorescence microscopy with resolution that is conceptually not limited by diffraction.
Yet diffraction plays a role in these ‘diffraction-unlimited’ techniques because the resolution of these ‘nanoscopy’ methods still benefits strongly from focusing the light as sharply as possible. While in STED and RESOLFT, it is the focusing of the illumination light in sample space that matters, in PALM/STORM it is the focusing of the emitted light at the detector. Therefore, the optimization of focusing remains very timely. 4Pi arrangements can also facilitate the doubling of the detected fluorescence without compromising the resolution in the focal plane (x,y), and offer significantly sharper axial (z) intensity gradients than single lenses for both the illumination and the detected light. Consequently, the combination of 4Pi with STED, RESOLFT and PALM/STORM approaches currently offers the most powerful optical setting for three-dimensional (3D) fluorescence nanoscopy5,6,7.
Yet 4Pi-type super-resolution arrangements are scarcely reported for STED and PALM and entirely unexplored for RESOLFT, a STED-derivative that typically uses reversibly switchable fluorescent proteins (RSFP) for providing the mandatory ON and OFF states. RSFP-based RESOLFT is particularly attractive because it operates with low light levels, making it gentle to living cells8.
The difficulties of realizing a 4Pi setup are commonly attributed to the counter-alignment of the two high numerical aperture (NA) lenses. In practice, however, the alignment can be controlled and stabilized over many hours. Instead, a far more general problem that is inherent to all fluorescent imaging modalities comes to the fore. The fluorescence signal (that emanates from each sub-diffraction pixel volume under investigation) needs to be discriminated against ‘background’ signal from outside of this volume. This ‘background’ largely stems from optical aberrations that preclude precise spatial control of the illumination or fluorescence beam positions and, in case of STED, RESOLFT or PALM/STORM, from imperfections of the ON/OFF-state transfer (switching) process. Discrimination against this ‘background’ signal is most challenging along the optical (z) axis, especially when the probed volume is of sub-diffraction dimensions. Lack of sufficient discrimination along the z-axis (optical sectioning) manifests itself as artifacts in the image, particularly as ‘ghost features’ above and below the real features.
When describing the imaging process in the spatial frequency domain, the appearance of axial lobes corresponds to local depressions in the amplitude of the optical transfer function, that is, the modulation transfer function (MTF) of the microscope. Structural information of the sample can only be retrieved in those spatial frequency bands where the MTF is strong enough to convey a signal that sufficiently exceeds the local noise level. In a 4Pi microscope, MTF depressions are typically restricted to sharp local minima at the so-called critical frequencies9. As their amplitude strongly depends on the aperture angle α of the objective lenses used9, combinations of 4Pi with diffraction-unlimited super-resolution/nanoscopy methods such as isoSTED5,10,11 and iPALM6,12, have unfortunately been limited to imaging fixed samples that are more easily accessible with high angle lenses (α≥74°, as for oil immersion lenses with NA≥1.46). Furthermore, the imaged objects were rather thin and labelled very sparsely, as both properties alleviate the requirements on optical sectioning, that is, on suppressing (‘background’) signal from above and below the focal plane. Fortunately, in a coordinate-targeted nanoscopy method such as RESOLFT, the signal received from the targeted nanosized pixel volume scales with the average number of molecules located within this volume, allowing for tailoring of the pixel volume11, and hence the resolution and the signal, to the actual imaging conditions to render the ‘background’ (mathematically) treatable.
Here we report the realization of 4Pi-RESOLFT nanoscopy, that is, of a conceptually diffraction-unlimited resolving method which, by virtue of 4Pi microscopy, provides spatially uniform 3D resolution for imaging (living) cells at the nanometre scale, offers strong optical sectioning due to multiple background suppressing mechanisms and operates at low light levels in 3D.
On-switching order and optical sectioning
The effective point-spread-function (PSF) hef(r) of a coordinate-targeted superresolution imaging modality ultimately quantifies the 3D-coordinate range where the fluorescent molecules are allowed to yield measurable signal. If the fluorophores from a certain range are imaged onto a (confocal point) detector, hef(r) is given by the normalized distribution SON(r) showing where a molecule is allowed to be in the ON-state at the time of read-out, multiplied by a normalized function hdet(r) that describes the detection probability:
SON(r) is proportional to a product of normalized terms hon and that describe the generation of the ON-state by the use of on- and off-switching processes, respectively. hon describes the spatial probability to assume the ON-state in the absence of off-switching light. It can typically be written as a product of terms that each express the relative probability for absorption of a single photon that drives a transition to a (virtual) state, and therefore scales with the intensity of the light patterns used (for example, for single-photon excitation with intensity ; in case of two-photon excitation: ). describes the effect of the off-switching light on a potential ON-state distribution; where molecules are always allowed to assume the ON-state, and where they are forced to stay in an OFF-state. Due to the forced assumption of an OFF-state by ‘saturating’ off-switching, is usually much sharper than the off-switching light intensity patterns.
We formally define hdet as the first on-switching term (because of its similar effect on hef), drop any that does not significantly sharpen hef (for example, widefield-detection or sample-wide switching) and obtain:
Here the number of on-factors Oon denotes the on-(switching) order of hef, for example, Oon=2 (excitation by single-photon absorption and confocal detection) for a typical confocal (STED) microscope. Optical sectioning can generally be improved by engineering such that molecules in out-of-focus areas are switched off more effectively (Supplementary Fig. 1), or by requiring the absorption of multiple photons for the occupation of the ON-state, which increases Oon. The latter can be realized directly through standard two-photon absorption13,14,15,16,17, or by requiring the sequential occupation of multiple real states to reach the ON-state18. Such sequential state occupation is easily realized using the switching steps offered by RSFP (that are central to the RSFP-based RESOLFT concept4,19).
The 4Pi-RESOLFT modality
In this study, we devised a coordinate-targeted 4Pi-RESOLFT modality that utilizes negative-switching RSFP (that is, those that are switched off at a wavelength that is also used for generating the fluorescent signal, Fig. 1a) and that resorts to all the processes mentioned above for strong optical sectioning. Concretely, we opted for the RSFP Dronpa-M159T20,21,22, which stands out by relatively fast switching kinetics with comparatively low background. At each scanning position, the local RSFP molecules were cycled through their ON- and OFF-states by consecutive light pulses that defined our RESOLFT imaging sequence (Fig. 1a). In the initial step (‘activation’ pulse), we applied a μs-long train of 170–fs pulses at 90 MHz/780 nm in a focal pattern hac to (partially) transfer (’activate’) local RSFP to their meta-stable ‘active’-state by two-photon absorption, as described by the activation distribution SB(r). Subsequently, we applied a μs–ms-long ‘deactivation’ pulse of continuous-wave (CW) irradiation at 488 or 491 nm, focused to form a hollow deactivation pattern (for example, a ‘z-donut’ hzd, Fig. 1a, Supplementary Methods). This drove active RSFP outside the targeted pixel volume (for example, above and below the focal plane) back to their inactive state, which effectively denied them a further excitation to the fluorescent ON-state and thus improved the spatial ON/OFF-contrast during the following ‘read-out’ pulse. We finally probed the remaining active RSFP by a second μs–ms-long CW pulse at 491 nm with a focal pattern hro, which transferred them to their fluorescent (ON) state, and detected the fluorescence through a confocal pinhole.
Our scheme thus entails a number of advantages for live-cell 3D-imaging. First, RSFP are inherently live-cell compatible protein markers, and selection of sufficiently bright and stable RSFP is readily available8,20,23. Second, optical sectioning benefits from the additional switching step (activation) involved in the RSFP switching cycle with respect to modalities that do not make use of a meta-stable state. This additional switching becomes especially powerful if it is mediated by two-photon absorption in a 4Pi configuration, as Oon rises to 4 and the activation and read-out patterns (hac, hro) can be setup to a limited zone of overlap in the focal region (Fig. 1a). While overlapping several pattern also forms the basis of 4Pi microscopy of type C using two-photon excitation24, here we do not require coherent double-lens (4Pi) detection of the emitted fluorescence, and therefore do not need broad-band intra-cavity dispersion compensation. The scheme presented here thus acts to the same effect with much less technical complexity. Finally, activation by two-photon absorption entails much less photo damage than two-photon excitation, as it takes place at a time during the switching cycle when virtually no markers can assume their excited fluorescent state.
Under ideal conditions, the effective PSF hef of such a system is virtually free of axial lobes (Fig. 1a) even without a deactivation pulse. In practice, incomplete deactivation and optical aberrations may give rise to lobe amplitudes that are still relevant. To counteract these effects, we applied dedicated lobe deactivation by hzd and developed low-aberration25, live-cell 4Pi optics (Fig. 1b, Methods). These measures enabled volume scans of over 5-μm-thick mammalian cells without noticeable bleaching at an axial (z) resolution in the 100 nm range and axial lobes of only ∼15% of the main peak of the z-response, that is, measured on laterally (xy) integrated data (Fig. 2). The base acquisition time of 7–21 s μm−3 (depending on the brightness of the labelled structure) was short enough to capture the subtly moving cytoskeleton of a living cell (Fig. 2b,c, total acquisition times incl. drift correction overhead b: 115 min per 703 μm3, c: 160 min per 400 μm3). For highly mobile organelles, such as mitochondria (Fig. 2a), fixation of the sample by paraformaldehyde incubation (Supplementary Methods) offered a means to prevent motion blur. While this treatment irreversibly arrests the cell, its potential to introduce structural artifacts is very low with respect to staining/embedding protocols that involve membrane permeabilization.
To resolve smaller features, we implemented a second switching pattern for deactivation of RSFP around the focal centre: A hollow ‘3D-donut’ h3d (Fig. 3a), created by a single focused 4Pi beam pair26 (Methods), allowed us to tune hef to a near-isotropic resolution below the diffraction limit (Fig. 3a). Calculations using a vectorial diffraction theory27 predicted on-axis MTF values of over 40% of the MTF maximum within the MTF bandwidth up to a resolution of 30 nm. This feature keeps the signal well over the noise level in most applications and exemplifies the improvement brought about by higher order on-switching in comparison to modalities of second order such as those reported in isoSTED microscopy5 (Fig. 3b). Furthermore, the confinement of the fluorescent on-state, that is, of hef, to sub-diffraction 3D volumes means that fewer fluorophores are interrogated at any point in time. This reduction in number of interrogated molecules (that are inherently co-localized) greatly facilitates the quantitative assessment of the properties of the fluorescent labels as they vary in the sample. We found that in time-resolved recordings, the on/off separation contrast decayed over time, hinting to the contribution of multiple deactivation rates. Thus, we introduced a ‘rate-gated’ RESOLFT detection scheme that improved both the signal-to-noise ratio in the image and the resolution by discriminating individual signal components (Fig. 3c,d, Methods).
Following this approach, we recorded images of Lifeact-Dronpa-M159T-expressing cells and adjusted rate-gating and the RESOLFT pulse sequence for target resolutions of 30-50 nm; the parameters were established by a PSF simulation using measured rate kinetics. Optical xz-sections taken perpendicular to the run of solitary actin fibre bundles confirmed the effectiveness of rate-gating (Fig. 3c,d) and the overall shape of the effective PSF (Fig. 3e). Illumination with the z-donut-shaped (hzd) focus for 1 ms at an average light power of 1.8 μW (488 nm, CW) was sufficient to virtually eliminate lobe background from the image (Fig. 3e, +hzd), while the low gradients around the central zero of hzd with respect to h3d facilitated the mutual alignment of these patterns (Supplementary Fig. 1). Turning to the finer structured actin network inside the cell body, we measured apparent feature sizes well below 40 nm (Fig. 4a–c). At a relaxed target resolution of 50 nm and an acquisition time of 3.3 min μm−2, we observed the time evolution of the actin scaffold at a vertical contact region of two neighbouring cells (Fig. 4e–g).
Using the current RSFP Dronpa-M159T, rate-gating allowed us to obtain images based on-switching speeds (switch-off half-time T1/2=10–17 μs at 11.5 kW cm−2 illumination intensity, Fig. 3c, Supplementary Fig. 2, Supplementary Table 1) that were over an order of magnitude faster than the previously reported corresponding values for rapid switching RSFP (T1/2, rsEGFP2: 250 μs (ref. 23), Dronpa-M159T: 230 μs (ref. 28)). Still the recording speed of our 4Pi-RESOLFT nanoscopy scheme can be made substantially faster by parallelization using a multi-spot scanning arrangement. In this case, the recording time of a certain sample area or volume would be cut down by the number of individual recording channels, that is, by the degree of parallelization.
In this study, we opted for cellular structures that are more demanding for 3D-superresolution imaging due to their high spatial density and wide axial extension. Under conditions exacerbated by the optical inhomogeneity of living cells, the signal from a (sub-diffractive) ensemble is easily buried in background (lobe) fluorescence beyond recovery. Nevertheless, owing to the consistently robust MTF of our 4Pi-RESOLFT scheme (Fig. 3b), we obtained raw (Fig. 2, insets) and rate-gated image data (Fig. 4e–g) that were conclusive without the mathematical post-processing (that is, deconvolution) dedicated to lobe-removal that is usually applied in 4Pi-based methods. The actin network seen in the exemplary time-lapse recording (Fig. 4e–g) appeared particularly crowded and extended over 8 μm along the optic axis, which forced the light to pass through several micrometres of cellular material from all angles. Still, the rearrangement of the entwined actin fibres could be traced in great detail, which was possible because the obtained images were practically devoid of axial lobes.
Notably, our scheme of reducing the global refractive index (RI) variance (Fig. 1b) turned out to sufficiently mitigate sample-induced aberrations without adding the complexity associated with adaptive optical elements. The most prominent residual aberration effect was a position-dependent 4Pi phase offset that stemmed from the uneven thickness of the cell layer; it has been accounted for during our recordings by the automated correction mechanism that also counteracted thermal drift (Supplementary Methods).
In conclusion, by realizing 4Pi-RESOLFT nanoscopy based on RSFPs, we have demonstrated exceptional optical sectioning in coordinate-targeted far-field fluorescence nanoscopy, which greatly facilitates nanometre scale 3D fluorescence imaging in living cells. Many accepted constraints to the sample can be lifted, which opens up an imaging regime that has so far been systematically avoided.
4Pi sample optics for live-cell imaging
In a 4Pi arrangement, the RI (n) difference between the material forming a living mammalian cell (n≈1.35–1.40) and the surrounding culture medium (typically n≈1.33) is a major source of optical aberrations. Aberrations generally reduce the attainable signal-to-noise ratio (S/N) by blurring the light intensity distributions in the focal region and by raising the intensity of the central minimum of the off-switching light patterns (Figs 1a and 3a). We therefore devised a mounting procedure that minimizes optical aberrations by raising the RI of a standard cell culture medium to n=1.362 (Supplementary Fig. 3, Supplementary Methods) and by designing the optical setup accordingly (Fig. 1b, Supplementary Figs 4 and 5): The 4Pi foci are jointly created by two 1.20 NA water immersion objectives that are outfitted with individual tip/tilt-correction to prevent aberrations that arise from lens-coverslip misalignment29. The refractive indices of the embedding (n=1.362) and immersion media (n=1.350), the correction collar settings and the cover slip thickness were chosen to minimize spherical aberrations25 over at least 10 μm of sample depth. The changes in the optical path lengths of the two 4Pi-interferometer arms due to z-scanning of the sample were compensated30 by synchronous position adjustment of the main beam splitter cube (Supplementary Fig. 4).
A single-focus 3D light pattern for deactivation
To resolve features smaller than 100 nm, we added a RSFP deactivation beam to the microscope. It was imprinted with a circular phase ramp that was subsequently imaged into the back pupil planes of both objective lenses. In contrast to the configuration of a single-lens RESOLFT setup, the direction of rotation of the phase ramp was oriented in countersense with respect to the circular beam polarization at the back pupil planes, which produced a 4Pi off-switching pattern h3d that completely surrounded a central zero26 (Fig. 3a). Applying h3d during the deactivation phase of the RESOLFT switching cycle squeezed the central full width at half maximum (FWHM) def of hef and allowed us to tune hef to a resolution below the diffraction limit.
RESOLFT imaging with rate-gated detection
In the present case of RESOLFT imaging of negative-switching RSFP, deactivation of fluorophores during read-out gives rise to a time-dependent signal and hence a time-dependent effective PSF hef(r,t). The time-resolved image g(r,t) obtained by imaging a structure s(r) is thus given by
We simplistically assume a deactivation rate λ(r) that only depends on the read-out intensity Iro(r) and therefore obtain
with t denoting time relative to the start of the read-out pulse. The deactivation pattern h3d(r) typically confines the effective volume from which fluorescence is collected to a region of FWHM def around the primary zero of the deactivation pattern. This region is much narrower than the FWHM dro of the diffraction pattern used for read-out:
The read-out intensity can then be considered constant, and hef(r,t) follows a mono-exponential decay at a rate that only depends on the peak read-out intensity . Thus, g(r,t) becomes separable and transforms into:
Data from test structures, however, exhibit a distinct multi-exponential behaviour that requires additional components for a proper fit (Fig. 3c):
where n components with ordered switching rates , and coefficients are fitted to the data (‘^’ marks fit results). While we attribute the fastest rate to signal from unimpaired RSFP at the focal centre, the presence of additional rates suggests the co-existence of RSFP species that exhibit significantly slower switching kinetics. A slowed-down switching observed after fixation supports this notion. Unintended processes during image recording also potentially contribute to the observed signal behaviour, for example, the re-activation of RSFP by the read-out light which generates a constant background.
Without loss of generality, we assume a position independent mixture of n species with discrete switching rates λj. Since the deactivation pattern h3d shrinks the effective PSF by a λ-dependent factor, hef(r,t) has to be generalized to a superposition of n individual that each correspond to a λj. Furthermore, we assume our experimental parameters are chosen such that the in-focus part hfast of obeys the analogue to equation (5), and pool the remaining contributions in hslow:
Consequently, the apparent resolution of the acquired image is less than the potential resolution provided by hfast and declines over time, as faster components vanish first (Fig. 3c).
To access the full image information that is mediated by hfast, we implemented an unmixing scheme that isolates the fastest switching signal component (rate λ0), and that we hence termed ‘rate-gating’: according to equation (3), the image generated by a PSF equation (8) takes on the form
whereby gslow is represented by a continuum of exponentials with switching speeds Λ∈[0,λ1] and coefficients c(r,Λ) as the result of s⊗hslow.
Hence, a fit to an imaged structure according to equation (7), in principle, provides a position invariant estimate for by , on top of a local approximation of gslow(r,t). In practice however, an insufficient photon count often prohibits local fitting of equation (9). We therefore implemented a robust approximation scheme for gfast(r) that only relies on parameters that can be extracted from a fit to the global (that is, from a region much larger than the corresponding diffraction limit) spatial average of the measured data:
First, we estimated the time t0 at which the integrated signal exhibits the maximum S/N with respect to gfast:
Locally calculated values for t0 would slightly differ, but as this only affects the statistical error of the result, equation (10) is usually sufficiently precise. Second, we determined a cut-off time t1 such that
which is usually the case for t1=2t0. By further choosing t2 and t3 such that ti>ti+1(i=0..3), we partition the measured signal into time bins ∑0,1,2 (Fig. 3d),
with F(r) and S(r) denoting the time integrals over the fast and slow components:
Finally, we estimated F(r), and thereby g0(r), by linear extrapolation in either zeroth or first order:
with u,v=u,v(t0..3) denoting geometrical factors that account for the particular choice of the t0..3. Narrowing the integration intervals defined by t0..3 and moving them closer to t=0, just as the inclusion of the first extrapolation order, reduces the systematic error, but also raises the statistic error due to a reduced photon count. To mitigate this effect, and owing to equation (11), we substituted ∑1,2 with their respective resolution-neutral local averages, for example, by applying a Gaussian filter with a FWHM sufficiently far below the FWHM of .
How to cite this article: Böhm, U. et al. 4Pi-RESOLFT nanoscopy. Nat. Commun. 7:10504 doi: 10.1038/ncomms10504 (2016).
Hell, S. W. Double-confocal scanning microscope. European Patent 0491289. (1992).
Hell, S. W. & Stelzer, E. H. K. Properties of a 4pi confocal fluorescence microscope. J. Opt. Soc. Am. A Opt. Image Sci. Vis. 9, 2159–2166 (1992).
Gustafsson, M. G. L., Agard, D. A. & Sedat, J. W. Sevenfold improvement of axial resolution in 3D widefield microscopy using two objective lenses. Proc. Soc. Photo-Opt. Instrum. Eng. 2412, 147–156 (1995).
Eggeling, C., Willig, K. I., Sahl, S. J. & Hell, S. W. Lens-based fluorescence nanoscopy. Q. Rev. Biophys. 48, 178–243 (2015).
Schmidt, R. et al. Spherical nanosized focal spot unravels the interior of cells. Nat. Methods 5, 539–544 (2008).
Shtengel, G. et al. Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure. Proc. Natl Acad. Sci. USA 106, 3125–3130 (2009).
Hell, S. W., Schmidt, R. & Egner, A. Diffraction-unlimited three-dimensional optical nanoscopy with opposing lenses. Nat. Photon. 3, 381–387 (2009).
Grotjohann, T. et al. Diffraction-unlimited all-optical imaging and writing with a photochromic GFP. Nature 478, 204–208 (2011).
Lang, M. C., Engelhardt, J. & Hell, S. W. 4Pi microscopy with linear fluorescence excitation. Opt. Lett. 32, 259–261 (2007).
Schmidt, R. et al. Mitochondrial cristae revealed with focused light. Nano Lett. 9, 2508–2510 (2009).
Ullal, C. K., Schmidt, R., Hell, S. W. & Egner, A. Block copolymer nanostructures mapped by far-field optics. Nano Lett. 9, 2497–2500 (2009).
Kanchanawong, P. et al. Nanoscale architecture of integrin-based cell adhesions. Nature 468, 580–584 (2010).
Denk, W., Strickler, J. H. & Webb, W. W. 2-photon laser scanning fluorescence microscopy. Science 248, 73–76 (1990).
Schneider, M., Barozzi, S., Testa, I., Faretta, M. & Diaspro, A. Two-photon activation and excitation properties of PA-GFP in the 720-920-nm region. Biophys. J. 89, 1346–1352 (2005).
Glaschick, S. et al. Axial resolution enhancement by 4Pi confocal fluorescence microscopy with two-photon excitation. J. Biol. Phys. 33, 433–443 (2007).
Moneron, G. & Hell, S. W. Two-photon excitation STED microscopy. Opt. Express 17, 14567–14573 (2009).
York, A. G., Ghitani, A., Vaziri, A., Davidson, M. W. & Shroff, H. Confined activation and subdiffractive localization enables whole-cell PALM with genetically expressed probes. Nat. Methods 8, 327–333 (2011).
Hell, S. W. Improvement of lateral resolution in far-field light microscopy using two-photon excitation with offset beams. Opt. Commun. 106, 19–24 (1994).
Hell, S. W. Toward fluorescence nanoscopy. Nat. Biotechnol. 21, 1347–1355 (2003).
Stiel, A. C. et al. 1.8 angstrom bright-state structure of the reversibly switchable fluorescent protein dronpa guides the generation of fast switching variants. Biochem. J. 402, 35–42 (2007).
Willig, K. I., Stiel, A. C., Brakemann, T., Jakobs, S. & Hell, S. W. Dual-label STED nanoscopy of living cells using photochromism. Nano Lett. 11, 3970–3973 (2011).
Testa, I. et al. Nanoscopy of living brain slices with low light levels. Neuron 75, 992–1000 (2012).
Grotjohann, T. et al. rsEGFP2 enables fast RESOLFT nanoscopy of living cells. eLife 1, e00248 00241-00214 (2012).
Gugel, H. et al. Cooperative 4pi excitation and detection yields sevenfold sharper optical sections in live-cell microscopy. Biophys. J. 87, 4146–4152 (2004).
Wan, D. S., Rajadhyaksha, M. & Webb, R. H. Analysis of spherical aberration of a water immersion objective: application to specimens with refractive indices 1.33-1.40. J. Microsc. 197, 274–284 (2000).
Schmidt, R. 3D Fluorescence Microscopy with Isotropic Resolution on the Nanoscale PhD thesis, Univ. Heidelberg (2008).
Richards, B. & Wolf, E. Electromagnetic diffraction in optical systems. II. structure of the image field in an aplanatic system. Proc. R. Soc. Lond. A 253, 358–379 (1959).
Testa, I., D'Este, E., Urban, N. T., Balzarotti, F. & Hell, S. W. Dual channel RESOLFT nanoscopy by using fluorescent state kinetics. Nano Lett. 15, 103–106 (2015).
Arimoto, R. & Murray, J. M. A common aberration with water-immersion objective lenses. J. Microsc. 216, 49–51 (2004).
Hell, S. W., Schrader, M. & VanderVoort, H. T. M. Far-field fluorescence microscopy with three-dimensional resolution in the 100-nm range. J. Microsc. 187, 1–7 (1997).
We thank C. Gregor for providing the plasmid Lifeact-Dronpa-M159T, T. Gilat and E. Rothermel for cloning support and assistance with cell culture preparation, B. Thiel for Imspector software support and A. Pucher-Diehl for precision mechanic support for custom microscope parts. S.W.H. and R.S. acknowledge a grant by the Deutsche Forschungsgemeinschaft within SFB 775.
The authors declare no competing financial interests.
Supplementary Figures 1-5, Supplementary Table 1, Supplementary Methods and Supplementary References. (PDF 2620 kb)
tsCOX8a-Dronpa-M159T, targeted to mitochondria. Fixed-cell recording, 14.06 x 4.00 x 10.94 μm3 (xzy). (MPG 7424 kb)
Lifeact-Dronpa-M159T, targeted to actin. Live-cell recording, 28.13 x 6.25 x 4.00 μm3 (xzy). (MPG 7456 kb)
Vimentin-Dronpa-M159T. Prior to acquisition, three sample regions (centered at the medial xz-plane of the recorded volume) were deliberately exposed to coincident illumination of the activation and read-out light, which negated the bleaching protection introduced by the 2-photon-activation pulse scheme and consequently resulted in a local signal attenuation. Live-cell recording, 25.0 x 8.0 x 2.0 μm3 (xzy). (MPG 7424 kb)
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Böhm, U., Hell, S. & Schmidt, R. 4Pi-RESOLFT nanoscopy. Nat Commun 7, 10504 (2016). https://doi.org/10.1038/ncomms10504
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