Two-photon Fluorescence Enhancement Research Articles

Temperature-Modulated Evolution of Surface Structures Induces Significant Enhancement of Two-Photon Fluorescent Emission from a Dye Molecule.

Fluorescence is an essential property of molecules and materials that plays a pivotal role across various areas such as lighting, sensing, imaging, and other applications. For instance, temperature-sensitive fluorescence emission is widely utilized for chemo-/biosensing but usually decreases the intensity upon the increase in temperature. In this study, we observed a temperature-induced enhancement of up to ∼150 times in two-photon fluorescence (TPF) emission from a dye molecule, 4-(4-diethylaminostyry)-1-methylpyridinium iodide (D289), as it interacted with binary complex vesicles composed of two commonly applied surfactants: sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB). By employing second harmonic generation (SHG) and TPF techniques, we clearly revealed the temperature-dependent kinetic behavior of D289 on the surface of the vesicles and utilized it to interpret the origin of the significant TPF enhancement. Additionally, we also demonstrated a similar heating-induced enhancement of the TPF emission from D289 on the membrane of phospholipid vesicles, indicating the potential application of TPF in temperature sensing in the biology systems. The embedding of D289 in the tightly packed alkane chains was identified as the key factor in enhancing the TPF emission from D289. This finding may provide valuable information for synthesizing fluorescence materials with a high optical yield.

Two-Photon-Excited Single-Molecule Fluorescence Enhanced by Gold Nanorod Dimers.

We demonstrate two-photon-excited single-molecule fluorescence enhancement by single end-to-end self-assembled gold nanorod dimers. We employed biotinylated streptavidin as the molecular linker, which connected two gold nanorods in end-to-end fashion. The typical size of streptavidin of around 5 nm separates the gold nanorods with gaps suitable for the access of fresh dyes in aqueous solution, yet small enough to give very high two-photon fluorescence enhancement. Simulations show that enhancements of more than 7 orders of magnitude can be achieved for two-photon-excited fluorescence in the plasmonic hot spots. With such high enhancements, we successfully detect two-photon-excited fluorescence for a common organic dye (ATTO 610) at the single-molecule, single-nanoparticle level.

Enhancement of Two-Photon Fluorescence and Low Threshold Amplification of Spontaneous Emission of Zn-processed CuInS2 Quantum Dots

Heavy-metal-free I-III-VI2 quantum dots (QDs) have recently emerged as favorable alternatives to toxic II-VI QDs for optoelectronic and biological applications, but low fluorescence efficiency is a key issue related to the promising nanocrystals. In this work, we demonstrate big enhancement of two-photon fluorescence efficiency and low threshold two-photon pumped amplification of spontaneous emission (ASE) of Zn-processed CuInS2 (CIS) QDs for the first time. The change of two-photon process caused by Zn2+ cation exchange in CIS QDs is systematically investigated. Two-photon ASE in Zn-processed CIS QDs films is achieved with a record of low threshold fluence of 5.7μJ/cm^2. With high two-photon fluorescence quantum yields and low threshold ASE, the Zn-processed CIS QDs could become a promising candidate for two-photon bio-imaging, nonlinear optical and novel QDs laser devices.

Mitochondria-targeted iridium (III) complexes as two-photon fluorogenic probes of cysteine/homocysteine

Fluorescent imaging of cysteine (Cys) and homocysteine (Hcy) is crucial to understand sulphur metabolism in living cells. Whereas two-photon active cyclometalated Ir(III) complex for detecting Cys/Hcy has been rarely reported. Herein, two novel cyclometalated iridium (III) complexes Ir1-Ir2 with different electron-donor were designed, synthesized and fully characterized as well as confirmed by single-crystal X-ray diffraction analysis, which could selectively react with Cys/Hcy, accompanying with an obvious one- and two-photon fluorescence enhancement in vitro. The mechanism for sensing Cys/Hcy was further analyzed in detail by mass spectra and time-dependent density functional theory calculations. It was found that Ir2, bearing ester group, exhibited higher performance on the selective detection of Cys and Hcy compared to Ir1. Notably, the two-photon action cross-section value in the near-infrared region (∼800nm) of Ir2 is significantly enhanced upon the addition of Cys/Hcy. Further application to cellular imaging indicated that Ir2 is membrane permeable and capable of monitoring the changes of intracellular mitochondrial Cys/Hcy. These results support that such two-photon active complexes might provide a promising platform for the detection of mitochondrial Cys/Hcy in living biological systems.

Localizable and photoactivatable fluorophore for spatiotemporal two-photon bioimaging.

Photoactivatable probe-based fluorescent imaging has become an efficient and attractive technique for spatiotemporal microscopic studies of biological events. However, almost all previously reported photoactivatable organic probes have been based on hydrosoluble precursors, which have produced water-soluble active fluorophores able to readily diffuse away from the photocleavage site, thereby dramatically reducing spatial resolution. Hydroxyphenylquinazolinone (HPQ), a small organic dye known for its classic luminescence mechanism through excited-state intramolecular proton transfer (ESIPT), shows strong light emission in the solid state, but no emission in solution. In this work, HPQ was employed as a precursor to develop a localizable, photoactivatable two-photon probe (PHPQ) for spatiotemporal bioimaging applications. After photocleavage, PHPQ releases a precipitating HPQ fluorophore which shows both one-photon and two-photon excited yellow-green fluorescence, thereby producing a localizable fluorescence signal that affords high spatial resolution for bioimaging, with more than 200-fold one-photon and 150-fold two-photon fluorescence enhancement.

Plasmonic-enhanced two-photon fluorescence with single gold nanoshell

Single gold nanoshell with mutilpolar plasmon resonances is proposed to enhance two-photon fluorescence efficiently. The single emitter single nanoshell configuration is studied systematically by employing the finite-difference time-domain method. The emitter located inside or outside the nanoshell at various positions leads to a significantly different enhancement effect. The fluorescent emitter placed outside the nanoshell can achieve large fluorescence intensity given that both the position and orientation of the emission dipole are optimally controlled. In contrast, for the case of the emitter placed inside the nanoshell, it can experience substantial two-photon fluorescence enhancement without strict requirements upon the position and dipole orientations. Metallic nanoshell encapsulating many fluorescent emitters should be a promising nanocomposite configuration for bright two-photon fluorescence label. The results provide a comprehensive understanding about the plasmonic-enhanced two-photon fluorescence behaviors, and the nanocomposite configuration has great potential for optical detecting, imaging and sensing in biological applications.

Two-Photon Fluorescence Spectroscopy and Imaging of 4-Dimethylaminonaphthalimide Peptide and Protein Conjugates

We report detailed photophysical studies on the two-photon fluorescence processes of the solvatochromic fluorophore 4-DMN as a conjugate of the calmodulin (CaM) and the associated CaM-binding peptide M13. Strong two-photon fluorescence enhancement has been observed which is associated with calcium binding. It is found that the two-photon absorption cross-section is strongly dependent on the local environment surrounding the 4-DMN fluorophore in the CaM conjugates, providing sensitivity between sites of fluorophore attachment. Utilizing time-resolved measurements, the emission dynamics of 4-DMN under various environmental (solvent) conditions are analyzed. In addition, anisotropy measurements reveal that the 4-DMN-S38C-CaM system has restricted rotation in the calcium-bound calmodulin. To establish the utility for cellular imaging, two-photon fluorescence microscopy studies were also carried out with the 4-DMN-modified M13 peptide in cells. Together, these studies provide strong evidence that 4-DMN is a useful probe in two-photon imaging, with advantageous properties for cellular experiments.

Two‐Photon Fluorescence Imaging Super‐Enhanced by Multishell Nanophotonic Particles, with Application to Subcellular pH

A novel nanophotonic method for enhancing the two-photon fluorescence signal of a fluorophore is presented. It utilizes the second harmonic (SH) of the exciting light generated by noble metal nanospheres in whose near-field the dye molecules are placed, to further enhance the dye's fluorescence signal in addition to the usual metal-enhanced fluorescence phenomenon. This method enables demonstration, for the first time, of two-photon fluorescence enhancement inside a biological system, namely live cells. A multishell hydrogel nanoparticle containing a silver core, a protective citrate capping, which serves also as an excitation quenching inhibitor spacer, a pH indicator dye shell, and a polyacrylamide cladding are employed. Utilizing this technique, an enhancement of up to 20 times in the two-photon fluorescence of the indicator dye is observed. Although a significant portion of the enhanced fluorescence signal is due to one-photon processes accompanying the SH generation of the exciting light, this method preserves all the advantages of infrared-excited, two-photon microscopy: enhanced penetration depth, localized excitation, low photobleaching, low autofluorescence, and low cellular damage.

Two-photon fluorescence correlation spectroscopy with high count rates and low background using dielectric microspheres

Two-photon excitation fluorescence is a powerful technique commonly used for biological imaging. However, the low absorption cross section of this non-linear process is a critical issue for performing biomolecular spectroscopy at the single molecule level. Enhancing the two-photon fluorescence signal would greatly improve the effectiveness of this technique, yet current methods struggle with medium enhancement factors and/or high background noise. Here, we show that the two-photon fluorescence signal from single Alexa Fluor 488 molecules can be enhanced up to 10 times by using a 3 µm diameter latex sphere while adding almost no photoluminescence background. We report a full characterization of the two-photon fluorescence enhancement by a single microsphere using fluorescence correlation spectroscopy. This opens new routes to enhance non-linear optical signals and extend biophotonic applications.

Single- and Multiphoton Turn-On Fluorescent Fe3+ Sensors Based on Bis(rhodamine)

Selective and sensitive turn-on fluorescent Fe(3+) sensors based on novel bis(rhodamine) dye molecules are reported. The compounds are synthesized with very high yields and characterized with NMR, ESI mass spectrometry, and elemental analysis. Single- and two-photon fluorescence enhancement is observed for both molecules in the presence of Fe(3+). High selectivity and sensitivity is observed over other metal ions and is shown to be due mainly to the spirolactam ring-opening power of Fe(3+). All measurements are made in buffer environments simulating biological conditions to facilitate single- and multiphoton fluorescence imaging of Fe(3+) in vivo and in vitro. Larger enhancement of fluorescence for both one- and two-photon excitation makes them suitable candidates for fluorescent labeling of biological systems. Two photon cross-section and time-resolved fluorescence measurements are utilized to understand the selectivity of the present sensors for Fe(3+)-sensing.

Coherent enhancement in two-photon fluorescence in molecular system induced by phase-jump modulated pulse

Coherent control of two-photon fluorescence (TPF) of 2',7'-dichlorofluorescein in methanol solution was experimentally investigated by shaping the femtosecond pulse with the phase jump. The experimental results indicated that the TPF intensity induced by the shaped femtosecond pulses with certain phase jump could be coherently enhanced. The physical mechanisms for TPF enhancement in the molecular system were explicitly discussed and analyzed, which could be attributed to the wave-packet constructive interference in the excited states. Finally, two phase-locked femtosecond pulses were used to explore the wave-packet constructive interference in the excited states of 2',7'-dichlorofluorescein, which validate experimentally the proposed mechanism.

Photonic jet driven non-linear optics: example of two-photon fluorescence enhancement by dielectric microspheres

The two-photon excited fluorescence from a dye solution is enhanced when a small amount of micro-meter sized silica beads are added. This observation is made in the simple scattering regime (inter-sphere distance four times larger than their radius) and is shown to depend on the concentration of the silica spheres. For a solution of rhodamine B, the enhancement can reach more than 30 %. As complementary experiments show that the fluorescence efficiency is unchanged, we argue that the non-linear absorption is enhanced due to focussing of the incident beam in the near-field of the spheres, a situation previously referred to as photonic (nano-)jets [3]. Our calculations indeed show that for the parameters of the spheres studied near-field focussing leads to an intensity concentration close to the sphere surface. We suggest that these photonic jets could be used to enhance other non-linear optical effects.

Resonant double grating waveguide structures as enhancement platforms for two-photon fluorescence excitation

We report a strong enhancement of two-photon fluorescence (TPF) excitation in the evanescent field of a double grating waveguide structure (DGWS). For a suitable combination of wavelength, polarization, and angular orientation of the incident laser light DGWSs show resonant behavior resulting in a large field enhancement at the waveguide surface. We demonstrate that at resonance, TPF spectroscopy reveals a 330-fold enhancement of the fluorescence signal of a tetramethylrhodamine thin film prepared from a picomolar aqueous solution. This shows the large potential of DGWSs as TPF-based high-sensitivity sensor platforms for biotechnological and biophysical application.

Picosecond-pulse-induced two-photon fluorescence enhancement in biological material by application of grating waveguide structures

We report enhancement of two-photon fluorescence (TPF) excitation in fluorescent dyes and fluorescently labeled biomolecules by exploiting the optical properties of double grating waveguide structures (DGWSs). Picosecond laser pulses generate a large evanescent field based on the guided mode phenomenon in the resonant DGWSs, which induces strong TPF signals from fluorescent dyes at the waveguide surface. By recording enhanced TPF signals of Rhodamine B and Lucifer Yellow under resonance conditions, a detection sensitivity of concentrations of approximately one dye molecule per 0.1 microm2 was achieved. For the first time to our knowledge, enhanced TPF signals of a Lucifer Yellow-labeled biomolecule (human self-peptide) in an aqueous environment are demonstrated. These results strongly encourage the use of DGWSs as enhancement platforms in modern biophysics and biotechnology for investigations of biological membranes and cells.

Double grating waveguide structures: 350-fold enhancement of two-photon fluorescence applying ultrashort pulses

The enhancement of ultrashort pulse excited two-photon fluorescence (TPF) based on resonant double grating waveguide structures (DGWS) was studied systematically. For a specific wavelength, polarisation and angular orientation, the transmission of the incident light through these devices vanishes while most of the light is reflected by the structure. Since these resonances are based on a guided mode phenomenon they exhibit a large evanescent field inducing enormous TPF signals of, for instance, marker or biomolecules at the waveguide surface. TPF signals for various concentrations of Rhodamine B under and out of resonance conditions were recorded. We demonstrate a resonance enhancement of the monitored TPF of more than two orders of magnitude which can be achieved by DGWS specifically designed for ultrashort pulses without beam focussing or laser amplification. Furthermore, the observed enhancement increases with decreasing dye molecule concentration at the surface, so these structures can be considered as powerful platforms for TPF detection of even very small amounts of fluorescent molecules in biotechnology and spectroscopic applications.

Giant enhancement of two-photon fluorescence induced by resonant double grating waveguide structures

We report a 350-fold enhancement of ultra-short-pulse-excited two-photon fluorescence (TPF) using a resonant double grating waveguide structure (DGWS). These structures show vanishing transmission and maximum reflection under resonance conditions, i.e. specific wavelength, polarisation and angular orientation of the incident light. This guided mode phenomenon is characterised by a large field enhancement inducing an enormous TPF signal of fluorescent molecules at the waveguide surface, as compared to direct non-resonant excitation. We demonstrate that high spectral acceptance for ultra-short pulses with broad spectral bandwidths can be achieved by a specifically designed DGWS, and that neither beam focussing nor high laser power is necessary for TPF excitation. Due to the high enhancement of more than two orders of magnitude, DGWS can be considered as a powerful platform for TPF applications such as biosensing and microarray technology.