Light Of Wavelength Research Articles

Action spectrum for reorientations in bacteriorhodopsin of purple membrane in suspension

In the present study, the dependency of purple membrane (PM) dielectric responses on the wavelength of light in the range 380–750 nm has showed meaningful changes about the rotation of PM in suspension and about the rotation of bacteriorhodopsin (bR) trimer inside PM, as well. The action spectrum of PM random walk substantiates the existence of two states of bR. One of them (blue edge-state) lies at the blue edge and the other (red edge-state) at the red edge of the visible absorption of bR. The results might bear on correlation of these bands to some bR photocycle intermediates or bR photoproducts. The results implicate the protein–chromophore interactions that eventually underlie protein–lipid interactions. Disrupting the protein–lipid contact during the illumination with light of wavelength in ranges of (410–470 nm) and (610–720 nm) has resulted in emergence of distinct dielectric dispersion at 0.06–0.08 MHz which is comparable to the size of bR trimer or monomer.The work reports on the chromatic adaptation of bR in view of the dielectric spectral parameters of PM. It aimed to explore a correlation seemingly found between the light wavelength and the relaxations of bR trimer inside PM. Changes in rotational diffusion of bR trimer upon blue and red light illumination can influence the three dimensional data storage based on bR, which may implicate bR in bioelectronics.

Fabrication of Photoprocessable Materials via Photopolymerization Using an Acid-Induced Photocleavable Platinum-Acetylide Crosslinker.

Photopolymerization and photoprocessing are core technologies for molding and tuning polymer materials. However, they are incompatible with single materials owing to their contradictory photoreactivity. Herein, an acid-induced photocleavable crosslinker, a platinum-acetylide complex covered by permethylated cyclodextrins, enables the fabrication of photoprocessable materials via photopolymerization with N-(2-hydroxyethyl)acrylamide. The polymer networks are molded by 365 nm irradiation as well as softened and degraded by a cooperative reaction with HCl as an acidic additive under 365 nm UV light, or 470 nm visible light in the presence of a photosensitizer. Moreover, the crosslinker is applied to a photoadhesive triggered by 365 nm irradiation. The adhesion is detachable on-demand through acid-induced photodegradation with the same wavelength and intensity of irradiation. Thus, acid-induced photocleavage allows the integration of light-induced molding and processing under various lights of various wavelengths, opening up new strategies for polymer technologies.

Fabrication of Photoprocessable Materials via Photopolymerization Using an Acid‐Induced Photocleavable Platinum‐Acetylide Crosslinker

AbstractPhotopolymerization and photoprocessing are core technologies for molding and tuning polymer materials. However, they are incompatible with single materials owing to their contradictory photoreactivity. Herein, an acid‐induced photocleavable crosslinker, a platinum–acetylide complex covered by permethylated cyclodextrins, enables the fabrication of photoprocessable materials via photopolymerization with N‐(2‐hydroxyethyl)acrylamide. The polymer networks are molded by 365 nm irradiation as well as softened and degraded by a cooperative reaction with HCl as an acidic additive under 365 nm UV light, or 470 nm visible light in the presence of a photosensitizer. Moreover, the crosslinker is applied to a photoadhesive triggered by 365 nm irradiation. The adhesion is detachable on‐demand through acid‐induced photodegradation with the same wavelength and intensity of irradiation. Thus, acid‐induced photocleavage allows the integration of light‐induced molding and processing under various lights of various wavelengths, opening up new strategies for polymer technologies.

Sequential absorption of two photons creates a bistable form of RubyACR responsible for its strong desensitization

Channelrhodopsins with red-shifted absorption, rare in nature, are highly desired for optogenetics because light of longer wavelengths more deeply penetrates biological tissue. RubyACRs (Anion ChannelRhodopsins), a group of four closely related anion-conducting channelrhodopsins from thraustochytrid protists, are the most red-shifted channelrhodopsins known with absorption maxima up to 610nm. Their photocurrents are large, as is typical of blue- and green-absorbing ACRs, but they rapidly decrease during continuous illumination (desensitization) and extremely slowly recover in the dark. Here, we show that long-lasting desensitization of RubyACRs results from photochemistry not observed in any previously studied channelrhodopsins. Absorption of a second photon by a photocycle intermediate with maximal absorption at 640nm (P640) renders RubyACR bistable (i.e., very slowly interconvertible between two spectrally distinct forms). The photocycle of this bistable form involves long-lived nonconducting states (Llong and Mlong), formation of which is the reason for long-lasting desensitization of RubyACR photocurrents. Both Llong and Mlong are photoactive and convert to the initial unphotolyzed state upon blue or ultraviolet (UV) illumination, respectively. We show that desensitization of RubyACRs can be reduced or even eliminated by using ns laser flashes, trains of short light pulses instead of continuous illumination to avoid formation of Llong and Mlong, or by application of pulses of blue light between pulses of red light to photoconvert Llong to the initial unphotolyzed state.

Performance Enhancement of an Ag–Au Bimetallic SPR Sensor: A Theoretical and Experimental Study

Ag-Au bimetallic surface plasmon resonance (SPR) sensors operating in the Kretschmann configuration were investigated by numerical modelling and experiment. While Ag-based sensors have good sensitivity, they suffer from poor stability, and the addition of an Au capping layer offers improved chemical resistance and reliable analyte bonding via thiol-gold interactions. Sensors were evaluated with an Ag-Au combined thickness of 50 nm but different thickness ratios, and SPR reflectivity curves were obtained for 632.8 nm wavelength light incident over a range of angles. Numerical modelling using the transfer matrix method showed the SPR response improving as Au thickness decreased, giving the best results for 45 nm of Ag and 5 nm of Au. Experimental characterisation of fabricated Ag-Au bimetallic sensors was carried out with a custom SPR testbed. Performance parameters, including minimum reflectivity, FWHM, stability, and sensitivity were measured and the results were compared to those of single-layer Ag and Au sensors. A 5 nm Au coating was unable to preserve stable bimetallic sensor performance; however, increasing the Au thickness to 10 nm was sufficient to protect the Ag sensing layer, allowing only a small variation in the minimum reflectivity and FWHM when exposed to analytes for multiple hours. The sensitivity of the single-layer Ag, bimetallic Ag-Au, and Au sensors was measured as 3041%/Refractive Index Unit (RIU), 1817%/RIU, and 1229%/RIU, respectively. The sensitivity of the thickness-optimized bimetallic layer was ~1.5× that of the single-layer Au sensor.

Photoswitchable Inhibitors to Optically Control Specific Kinase Activity.

Potent and selective small-molecule inhibitors are valuable tools to elucidate the functions of protein kinases within complex signaling networks. Incorporation of a photoswitchable moiety into the inhibitor scaffold offers the opportunity to steer inhibitor potency with temporal precision, while the challenge of selective inhibition can often be addressed by employing a chemical genetic approach, termed the analog-sensitive method. Here, we combine the perks of these two approaches and report photoswitchable azopyrazoles to target calcium-dependent protein kinase 1 (CDPK1) from Toxoplasma gondii, a kinase naturally susceptible to analog-sensitive kinase inhibitors due to its glycine gatekeeper residue. The most promising azopyrazoles display favorable photochemical properties, thermal stability, and a substantial difference in IC50 values between both photostationary states. Consequently, the CDPK1 kinase reaction can be controlled dynamically and reversibly by applying light of different wavelengths. Inhibition of CDPK1 by the azopyrazoles drastically relies on the nature of the gatekeeper residue as a successive increase in gatekeeper size causes a concurrent loss of inhibitory activity. Furthermore, two photoswitchable inhibitors exhibit activity against T. gondii and Cryptosporidium parvum infection in a cell culture model, making them a promising addition to the toolbox for dissecting the role of CDPK1 in the infectious cycle with high temporal control. Overall, this work merges the benefits of the analog-sensitive approach and photopharmacology without compromising inhibitory potency and thus holds great promise for application to other protein kinases in the future.

Design and manufacturing of aspherical GaAs-SILs for a versatile optical semiconductor failure analysis system

In this study, we have developed an aspherical solid immersion lens (SIL) made of gallium arsenide (GaAs) for semiconductor failure analysis. A SIL is an optical component to dramatically increase the numerical aperture and the spatial resolution of a microscopy system by attaching it to the backside of the device-under-test. To further enhance the spatial resolution of the optical microscopy system, a shorter wavelength light source has also been introduced. In the past, we have developed a spherical SIL made of silicon (Si), which is the same material as the device under test. However, Si is not transparent for wavelengths shorter than around 1100 nm. To enable the use of a SIL at shorter wavelengths, we chose GaAs as SIL material, which is transparent at shorter wavelengths than Si and has a refractive index very close to that of Si. However, a spherical GaAs SIL features a more pronounced spherical aberration due to the difference in refractive index between the device-under-test (Si) and that of the SIL (GaAs) deteriorating the optical resolution of the microscopy system. We have therefore designed an aspherical GaAs-SIL which makes it possible to correct spherical aberration. We applied diamond tooling as a technique for manufacturing the SIL shape with a required surface irregularity below 100 nm peak-to-valley, resulting in a diffraction limited performance of the optical system for semiconductor failure analysis with a performance at around 0.18 μm cutoff.

An energy-saving glasshouse film reduces seasonal, and cultivar dependent Capsicum yield due to light limited photosynthesis

Glasshouse films can be used to reduce energy costs by limiting non-productive heat-generating radiation, but the impact on yield of greenhouse horticultural crops remains unknown. The effects of energy-saving film ULR-80 (ultra-low-reflectivity film with 80 % light transmission referred to as Smart Glass; SG) designed to block long wavelength light that generates heat also reduced photosynthetically active radiation (PAR) consequently affecting crop morphology, photosynthesis, leaf pigments, and yield of two hydroponically grown capsicum (Capsicum annuum L.) cultivars (Red and Orange). The crops were grown in four high-tech glasshouse bays over two seasons of similar daily light integrals (DLI) during ascending [Autumn Experiment (AE)] and descending [Summer Experiment (SE)] photoperiods. The Red cultivar exhibited higher photosynthetic rates (light saturated - Asat) and yield than the Orange cultivar in control glass but displayed stronger reductions in modelled photosynthetic rates at growth light and yield in SG without changes in photosynthetic capacity. Foliar pigment ratios of chlorophyll a/b and carotenoid:chlorophyll remained unaffected by the SG during both seasons indicating that chloroplast homeostasis was similar between SG and control. The seasonal differences in photosynthetic pigments and xanthophyll de-epoxidation state (DPS) revealed that cultivars were able to sense the SG-altered light environment during the AE, but not SE. The SE correlated with a lower daily light level and a substantial yield reduction of 29 % and 13 % in Red and Orange cultivars, respectively. Thus, SG-induced higher reductions in yield during the SE indicate that SG may be more beneficial for capsicum crops planted during AE.

Exploiting Reusable Edge‐Functionalized Metal‐Free Polyphthalocyanine Networks for Efficient Polymer Synthesis at Near Infrared Wavelengths

AbstractHeterogeneous catalysts are highly advantageous for industrial applications owing to their distinctive merits including easy separation and effective recovery. However, utilizing heterogeneous photocatalysts to harness longer wavelength light remains a critical area of research. This contribution explores the use of edge‐functionalized metal‐free polyphthalocyanine networks (PPc‐x) to promote efficient polymer synthesis under near infrared (NIR) light irradiation. Our screening process revealed that both phenyl‐edged PPc‐x (PPc‐p) and naphthyl‐edged PPc‐x (PPc‐n) offer promising performance for photopolymerization. With the assistance of ppm‐level PPc‐n catalyst, well‐defined polymers were synthesized within a few hours under the regulation of three NIR lights, regardless of shielded by synthetic and biological barriers. An excellent control over the molecular weight and molecular weight distribution was achieved. Furthermore, PPc‐x can be easily recovered and reused for multiple cycles, with negligible leaching and maintenance of the catalytic performance. This study expands a new avenue in developing versatile photocatalysts for the modern synthetic toolkits and offer benefits in diverse applications.

Exploiting Reusable Edge-Functionalized Metal-Free Polyphthalocyanine Networks for Efficient Polymer Synthesis at Near Infrared Wavelengths.

Heterogeneous catalysts are highly advantageous for industrial applications owing to their distinctive merits including easy separation and effective recovery. However, utilizing heterogeneous photocatalysts to harness longer wavelength light remains a critical area of research. This contribution explores the use of edge-functionalized metal-free polyphthalocyanine networks (PPc-x) to promote efficient polymer synthesis under near infrared (NIR) light irradiation. Our screening process revealed that both phenyl-edged PPc-x (PPc-p) and naphthyl-edged PPc-x (PPc-n) offer promising performance for photopolymerization. With the assistance of ppm-level PPc-n catalyst, well-defined polymers were synthesized within a few hours under the regulation of three NIR lights, regardless of shielded by synthetic and biological barriers. An excellent control over the molecular weight and molecular weight distribution was achieved. Furthermore, PPc-x can be easily recovered and reused for multiple cycles, with negligible leaching and maintenance of the catalytic performance. This study expands a new avenue in developing versatile photocatalysts for the modern synthetic toolkits and offer benefits in diverse applications.

Engineering nanoenzymes integrating Iron-based metal organic frameworks with Pt nanoparticles for enhanced Photodynamic-Ferroptosis therapy

Photodynamic therapy (PDT), as a promising strategy in cancer treatment that utilizes photosensitizers (PSs) to produce reactive oxygen species, has been widely used for eliminating cancer cells under specific wavelength light irradiation. However, the low aqueous solubility of PSs and special tumor microenvironments (TME), such as high glutathione (GSH) and tumor hypoxia remain challenges towards PDT for hypoxic tumor treatment. To address these problems, we constructed a novel nanoenzyme for enhanced PDT-ferroptosis therapy by integrating small Pt nanoparticles (Pt NPs) and near-infrared photosensitizer CyI into iron-based metal organic frameworks (MOFs). In addition, hyaluronic acid was adhered to the surface of the nanoenzymes to enhance the targeting ability. In this design, MOFs act not only as a delivery vector for PSs, but also a ferroptosis inducer. Pt NPs stabilized by MOFs were functioned as an oxygen (O2) generator by catalyzing hydrogen peroxide into O2 to relieve tumor hypoxia and increase singlet oxygen generation. In vitro and in vivo results demonstrated that under laser irradiation, this nanoenzyme could effectively relive the tumor hypoxia and decrease the level of GSH, resulting in enhanced PDT-ferroptosis therapy against hypoxic tumor. The proposed nanoenzymes represent an important advance in altering TME for improved clinical PDT-ferroptosis therapy, as well as their potential as effective theranostic agents for hypoxic tumors.

Artificial visual perception neural system using a solution-processable MoS2-based in-memory light sensor

Optoelectronic devices are advantageous in in-memory light sensing for visual information processing, recognition, and storage in an energy-efficient manner. Recently, in-memory light sensors have been proposed to improve the energy, area, and time efficiencies of neuromorphic computing systems. This study is primarily focused on the development of a single sensing-storage-processing node based on a two-terminal solution-processable MoS2 metal–oxide–semiconductor (MOS) charge-trapping memory structure—the basic structure for charge-coupled devices (CCD)—and showing its suitability for in-memory light sensing and artificial visual perception. The memory window of the device increased from 2.8 V to more than 6 V when the device was irradiated with optical lights of different wavelengths during the program operation. Furthermore, the charge retention capability of the device at a high temperature (100 °C) was enhanced from 36 to 64% when exposed to a light wavelength of 400 nm. The larger shift in the threshold voltage with an increasing operating voltage confirmed that more charges were trapped at the Al2O3/MoS2 interface and in the MoS2 layer. A small convolutional neural network was proposed to measure the optical sensing and electrical programming abilities of the device. The array simulation received optical images transmitted using a blue light wavelength and performed inference computation to process and recognize the images with 91% accuracy. This study is a significant step toward the development of optoelectronic MOS memory devices for neuromorphic visual perception, adaptive parallel processing networks for in-memory light sensing, and smart CCD cameras with artificial visual perception capabilities.

Comparison of the Penetration Depth of 905 nm and 1064 nm Laser Light in Surface Layers of Biological Tissue Ex Vivo.

The choice of parameters for laser beams used in the treatment of musculoskeletal diseases is of great importance. First, to reach high penetration depths into biological tissue and, secondly, to achieve the required effects on a molecular level. The penetration depth depends on the wavelength since there are multiple light-absorbing and scattering molecules in tissue with different absorption spectra. The present study is the first comparing the penetration depth of 1064 nm laser light with light of a smaller wavelength (905 nm) using high-fidelity laser measurement technology. Penetration depths in two types of tissue ex vivo (porcine skin and bovine muscle) were investigated. The transmittance of 1064 nm light through both tissue types was consistently higher than of 905 nm light. The largest differences (up to 5.9%) were seen in the upper 10 mm of tissue, while the difference vanished with increasing tissue thickness. Overall, the differences in penetration depth were comparably small. These results may be of relevance in the selection of a certain wavelength in the treatment of musculoskeletal diseases with laser therapy.

Compact multi-foci metalens spectrometer

A lightweight and portable spectrometer is desirable for miniaturization and integration. The unprecedented capability of optical metasurfaces has shown much promise to perform such a task. We propose and experimentally demonstrate a compact high-resolution spectrometer with a multi-foci metalens. The novel metalens is designed based on wavelength and phase multiplexing, which can accurately map the wavelength information into its focal points located on the same plane. The measured wavelengths in the light spectra agree with simulation results upon the illumination of various incident light spectra. The uniqueness of this technique lies in the novel metalens that can simultaneously realize wavelength splitting and light focusing. The compactness and ultrathin nature of the metalens spectrometer render this technology have potential applications in on-chip integrated photonics where spectral analysis and information processing can be performed in a compact platform.

Photoluminescence of Tb3+/Sm3+ ions co-activated in SrO - Na2O - WO3 - tellurite glasses for multicolor laser applications

A novel series of Tb3+, Sm3+ single doped and Tb3+/Sm3+ co-incorporated tungsten tellurite glasses were synthesized by melt quenching technique and corresponding structural as well as luminescence features of the prepared glasses have been reported here. Spectral overlapping between the luminescence spectra of Tb3+ ions and the excitation spectra of Sm3+ ions manifests that the energy transfer process takes place from Tb3+ ions to Sm3+ ions. By using the dual excitations at 377 and 484 nm, the titled co-doped glasses emit green light of wavelength 542 nm along with reddish – orange colour light at 599 nm. In addition to this, there is no possibility of reverse energy transfer which is validated with the help of excitation at 403 nm (Sm3+ ions) as major evidence. The lifetimes of all co-doped glasses decline with increasing Tb3+ doping level in the ligand matrices, indicating the energy migration process takes place from Tb3+→ Sm3+. The chromaticity coordinates of all synthesized co-doped glasses lie in yellowish-orange region of CIE1931 diagram and it shifts to deep yellow region when Tb3+ ion concentration varies. Our findings propose that the titled glasses can be used as visible laser materials for multicolor laser applications.

Open-circuit photopotential characterization of photoelectrochemical activities of Au-modified TiO2 nanorods

The open circuit potential (OCP) of a semiconductor electrode can be used to quantify the transient photopotential (Ep), which represents wavelength-dependent charge accumulation and relaxation kinetics of a photoelectrode. Here OCP responses of a plasmonic Au@TiO2 nanorods (NRs) photoelectrode can be quantified without causing electrochemical corrosion of Au. The photogenerated charge accumulation kinetics data based on the wavelength-dependent growth rates of |Ep| can resolve the plasmonic effects on photoelectrochemistry (PEC) of Au@TiO2 NRs. Data fitting with Kohlrausch-Williams-Watts (KWW) stretched exponential kinetics model illustrates the complex charge relaxations at the Au/TiO2 Schottky contact, from which long relaxation lifetimes with broad lifetime distributions can be obtained. This is attributed to the abundant deep defects in the nanostructure TiO2, which has been strongly confirmed by reducing the oxygen vacancies using a post-thermal annealing treatment. Single-particle dark-field scattering (DFS) spectrum is measured with a tunable wavelength light source to support visible light activities of PEC characteristics of Au@TiO2 NRs. Light scattering spectra of >200 single Au@TiO2 NRs particles are collected to compare directly with PEC responses of OCP of the ensemble Au@TiO2 NRs.

On the Nature of Stationary and Time-Resolved Fluorescence Spectroscopy of Collagen Powder from Bovine Achilles Tendon.

This paper presents a more systematic study of steady-state and time-resolved autofluorescence spectroscopy of collagen isolated from bovine Achilles tendon. In steady-state fluorescence measurements, the excitation and emission spectra of collagen powder, recorded at different fluorescence excitation and detection wavelengths, were compared with the fluorescence excitation and emission spectra of the amino acids phenylalanine, tyrosine, and tryptophan, as well as with similar spectra for 13 autofluorescent collagen cross-links, which have been identified and described in the literature so far. In time-resolved studies, fluorescence was excited by the pulsed light of different wavelengths, and for each excitation wavelength, fluorescence decay was recorded for several detection wavelengths. Data analysis allowed recovery of the fluorescence decay times for each experimental excitation detection event. The obtained information on the decay times of the measured fluorescent signals was discussed, taking into account the available literature data from similar studies of isolated collagen and collagen-rich tissues. Based on the obtained results, it was found that the shape and position of the measured fluorescence excitation and emission spectra of collagen strongly depend on the emission and excitation wavelengths selected in the measurements. From the recorded excitation and emission bands of collagen, it can be concluded with high probability that there are additional, so far unidentified, collagen cross-links, which can be excited at longer excitation wavelengths. In addition, the collagen excitation spectra were measured at longer emission wavelengths at which the collagen cross-links emit fluorescent light. In addition to the emission spectra obtained for excitation in the deep-UV region, the results of time-resolved fluorescence studies with excitation in the deep-UV region and detection at longer wavelengths suggest that fluorescence excitation energy transfer processes occur from the amino acids to the collagen cross-links, and also between the cross-links themselves.

Effect of post laser annealing on stacked structure of CZTS thin film solar cells

Cu2ZnSnS4 (CZTS) is an attractive material for thin film solar cells because all its constituents are Earth-abundant elements, and it’s a direct transition semiconductor with a band gap energy of 1.5 eV that is suitable for absorbing solar light spectrum effectively. CZTS is generally formed by precursor formation followed by heat treatment at 500 °C–600 °C to enhance the growth of crystal grain. In this work, a novel CZTS crystal grain re-growth process using post-laser annealing was investigated. 445 nm wavelength laser irradiation was performed on the Al-doped ZnO/CdS/CZTS/Mo/substrate stacked structure. X-ray diffraction and scanning microscope showed the CZTS crystal grain enlargement. Solar cells were fabricated on those structures and the external quantum efficiency was found to be improved especially at 500–1000 nm wavelength light absorption. That resulted in a short circuit current improvement.

Understanding the Molecular Conformation and Viscoelasticity of Low Sol-Gel Transition Temperature Gelatin Methacryloyl Suspensions.

For biomedical applications, gelatin is usually modified with methacryloyl groups to obtain gelatin methacryloyl (GelMA), which can be crosslinked by a radical reaction induced by low wavelength light to form mechanically stable hydrogels. The potential of GelMA hydrogels for tissue engineering has been well established, however, one of the main disadvantages of mammalian-origin gelatins is that their sol-gel transitions are close to room temperature, resulting in significant variations in viscosity that can be a problem for biofabrication applications. For these applications, cold-water fish-derived gelatins, such as salmon gelatin, are a good alternative due to their lower viscosity, viscoelastic and mechanical properties, as well as lower sol-gel transition temperatures, when compared with mammalian gelatins. However, information regarding GelMA (with special focus on salmon GelMA as a model for cold-water species) molecular conformation and the effect of pH prior to crosslinking, which is key for fabrication purposes since it will determine final hydrogel's structure, remains scarce. The aim of this work is to characterize salmon gelatin (SGel) and salmon methacryloyl gelatin (SGelMA) molecular configuration at two different acidic pHs (3.6 and 4.8) and to compare them to commercial porcine gelatin (PGel) and methacryloyl porcine gelatin (PGelMA), usually used for biomedical applications. Specifically, we evaluated gelatin and GelMA samples' molecular weight, isoelectric point (IEP), their molecular configuration by circular dichroism (CD), and determined their rheological and thermophysical properties. Results showed that functionalization affected gelatin molecular weight and IEP. Additionally, functionalization and pH affected gelatin molecular structure and rheological and thermal properties. Interestingly, the SGel and SGelMA molecular structure was more sensitive to pH changes, showing differences in gelation temperatures and triple helix formation than PGelMA. This work suggests that SGelMA presents high tunability as a biomaterial for biofabrication, highlighting the importance of a proper GelMA molecular configuration characterization prior to hydrogel fabrication.

Monitoring the Reversibility of GPCR Signaling by Combining Photochromic Ligands with Label‐free Impedance Analysis

AbstractG protein‐coupled cell surface receptors (GPCR) trigger complex intracellular signaling cascades upon agonist binding. Classic pharmacological assays provide information about binding affinities, activation or blockade at different stages of the signaling cascade, but real time dynamics and reversibility of these processes remain often disguised. We show that combining photochromic NPY receptor ligands, which can be toggled in their receptor activation ability by irradiation with light of different wavelengths, with whole cell label‐free impedance assays allows observing the cell response to receptor activation and its reversibility over time. The concept demonstrated on NPY receptors may be well applicable to many other GPCRs providing a deeper insight into the time course of intracellular signaling processes.