All-photonic kinase inhibitors: light-controlled release-and-report inhibition

Light-responsive molecular tools targeting kinases affords one the opportunity to study the underlying cellular function of selected kinases. In efforts to externally control lymphocyte-specific protein tyrosine kinase (LCK) activity, the development of release-and-report LCK inhibitors is described, in which (i) the release of the active kinase inhibitor can be controlled externally with light; and (ii) fluorescence is employed to report both the release and binding of the active kinase inhibitor. This introduces an unprecedented all-photonic method for users to both control and monitor real-time inhibitory activity. A functional cellular assay demonstrated light-mediated LCK inhibition in natural killer cells. The use of coumarin-derived caging groups resulted in rapid cellular uptake and non-specific intracellular localisation, while a BODIPY-derived caging group predominately localised in the cellular membrane. This concept of release-and-report inhibitors has the potential to be extended to other biorelevant targets where both spatiotemporal control in a cellular setting and a reporting mechanism would be beneficial.


Introduction
Light-responsive chemical probes have the potential to unveil the fundamental molecular events of complex cellular processes.In this context, light serves as a valuable non-invasive external stimulus and enables control of when and where drug activation occurs.][6][7][8][9][10][11][12] Photocaging has been a popular approach whereby a photolabile protecting moiety is strategically introduced onto a kinase inhibitor to prevent key interactions with their target enzyme.Inhibitory activity is only restored upon exposure to light and concomitant liberation of the active compound.5][6][7][8][9] While the use of uorescence caging groups that exhibit OFF-ON diagnostic changes in emission upon decaging have been employed to monitor the photorelease of caged substrates in a cellular environment, [13][14][15][16][17] the use of a 'reporting mechanism' for both photoactivation and binding of the decaged active inhibitor to the target kinase has yet to be fully explored.
The lymphocyte-specic protein tyrosine kinase (LCK) belongs to the Src family of non-receptor tyrosine kinases. 18,19role of LCK in both health and disease states with high spatiotemporal resolution are needed.The ability to manipulate the activity of LCK using light would result in spatiotemporal control of enzymatic activity, thus serving as a valuable tool to study LCK function.Furthermore, the visualisation of LCK inhibitors in live cells allows the user to monitor their therapeutic efficiency in real-time, providing further insight into e.g., their action mechanisms and the favoured subcellular localisation.
As a means to externally control LCK activity, as well as monitoring in real-time the photoactivation and the subsequent binding to the enzyme, we report the development of a series of caged LCK inhibitors where light is employed to: (i) trigger the release of the LCK inhibitor with high spatiotemporal resolution; (ii) monitor the decaging process, and; (iii) report the binding of the 'active' inhibitor to the LCK enzyme (Fig. 1).This has been achieved through the introduction of a photolabile caging moiety onto the previously reported solvatochromic LCK inhibitor 1, in which diagnostic changes in emission are observed upon binding the kinase enzyme (Fig. 1). 25In doing so, the caged form serves as a poor inhibitor of LCK while the intrinsic uorescence of the LCK inhibitor is quenched by electron and/or energy transfer mechanisms.Upon exposure to a certain wavelength of light, the caging group is cleaved to liberate the unbound form of the inhibitor which exhibits weak uorescence in aqueous solution.Only upon binding to the ATP-binding site of the LCK enzyme does the solvatochromic inhibitor exhibit a substantial increase in emission intensity and a blue-shi of the emission maximareporting back to the user that the inhibitor is bound to its target enzyme.More specically, two different classes of caging groups have been installed that are either (A) non-uorescent, or (B) uorescent (Fig. 1).While the former are 'spectroscopically silent' and simply mask the activity of 1 at both biological and photophysical levels, the incorporation of uorescent caging groups is envisioned to further assist the reporting of the release process.It was anticipated that the uorescence attributed to the caging group would be strongly quenched in the caged inhibitors.However, when exposed to light, the release of a highly emissive caging unit would allow for the convenient monitoring of the decaging process via a uorescence readout.

Design and synthesis of release-and-report kinase inhibitors
7][28] Therefore, the inclusion of a caging group at this position was pursued as it should prevent the formation of these key hydrogen bond interactions, rendering inhibitor 1 'inactive'.
Among the caging groups described in the literature, 29,30 those fullling the following criteria were selected: (i) applicability in biological contexts; (ii) can be cleaved at wavelengths that will not induce cellular damage (l > 320 nm); and (iii) the corresponding decaged product is non-toxic.As BODIPY-and coumarin-derived caging groups full these requirements, [29][30][31][32][33][34] the inclusion of such caging groups onto LCK inhibitor 1 via a carbamate linker was investigated.Due to the hydrophobic nature of coumarin-derived caging groups, the dimethylester-coumarin variant was also included in this study (compound 3c), as it was envisaged that the methylesters would serve as valuable synthetic handles for further functionalisation to tailor e.g., water solubility if required.Furthermore, the popular o-nitrobenzyl caging group was also included as despite their reliance on UV-light and the formation of a reactive decaged product, they have been widely utilised in a number of biological applications. 32,34The presence of a methyl group at the benzylic position of the o-nitrobenzyl caging group was also considered (compound 4b), as this would afford a ketone as the decaged product rather than the more reactive aldehyde.Thereby, the effect of the benzylic methyl group on the performance of the decaging reaction was of interest.
As shown in Scheme 1, the caged derivatives were synthesised by stirring activated carbonate building blocks 2a-e, LCK inhibitor 1 and HOBt in CH 2 Cl 2 at 40 °C (see ESI † for full synthetic details).Hydrolysis of the methyl ester in carbamates 3a and 3b with LiOH$H 2 O in THF/H 2 O (1 : 1) afforded caged derivatives 4a and 4b, respectively.

Photophysical evaluation of photocaged LCK inhibitors
The spectroscopic/photophysical data of 4a, 4b and 3c-e are summarised in Table 1.The emission properties of compounds 4a and 4b are comparable to those of 1 in terms of both spectral position and uorescence quantum yield.This shows that the caging groups used in these analogues are not signicantly affecting the spectroscopic properties of the caged conjugate.In contrast, caged inhibitors 3c-e equipped with intrinsically uorescent coumarin and BODIPY caging groups display weak uorescence, which originates from these building blocks rather than from the inhibitor itself.This is evident from the uorescent quantum yields, as these are slightly higher than that observed from 1 (Table 1).However, when compared to the corresponding coumarin and BODIPY model monomers (compounds S12, S16 and S20; Table S1 †), the uorescence in compounds 3c-e is indeed efficiently quenched.
To investigate whether photoinduced electron transfer (PET) can contribute to the uorescence quenching in the caged compounds 3c-e, electrochemical data of the model monomers were determined in acetonitrile or DMSO.The cyclic voltammograms are shown in Fig. S21.† All compounds were characterised by non-reversible or quasi-reversible electrochemical processes.The analysis according to the Rehm-Weller equation revealed that PET is thermodynamically favourable in the BODIPY-and coumarin-derived monomers (compounds S12, S16 and S20 in ESI †), thus fullling the design criteria detailed in Fig. 1.
The decaging reactions were evaluated in aqueous solution, in which DMSO was required to aid solubility (10% DMSO in H 2 O).Samples were irradiated with LEDs at 365 nm, 405 nm, or 523 nm depending on the absorption spectrum of the respective cage and the reactions were monitored by recording absorption spectra at regular intervals.
Upon analysis of the decaging reactions by UV/vis spectroscopy, it is evident that the overall kinetics are not always described by mono-exponential processes (Fig. S1 and S2 †).This observation is ascribed to the photo-or thermaldecomposition of the released products, including the decaged inhibitor 1 and the reactive species derived from the onitrobenzyl group.The notion of photodecomposition of the decaged inhibitor 1 is supported by the signicant spectral changes observed when LCK inhibitor 1 alone is irradiated with 365 nm (ca.30 mW cm −2 ) for 10 minutes (Fig. S5 †).This would imply that the absorption spectra recorded during photoirradiation of compounds 4a and 4b capture both the decaging and subsequent photodecomposition processes.It is therefore important to note that the reported decaging quantum yields may not be reective of a clean photolysis reaction and that these values will also be inuenced by any photodecomposition that may have occurred during these measurements.The inclusion of the methyl moiety on the benzylic position of the onitrobenzyl caging group substantially increases the decaging cross section (3$f dc , the product of molar absorption coefficient at the irradiation wavelength and decaging quantum yield).This is clearly seen when comparing the values for 4b (2 × 10 2 M −1 cm −1 ) and 4a (20 M −1 cm −1 , see Table 1).It is also interesting to note that the thermal stability increased   dramatically with the inclusion of the methyl group (4b, Fig. S10 †).The decaging cross section further increased for the coumarin-derived caged inhibitor 3c (2 × 10 3 M −1 cm −1 ) when compared to the o-nitrobenzyl derivatives.Due to the efficient nature of this decaging reaction, minimal photodegradation of active LCK inhibitor 1 was observed (Fig. S3 †).
The observed photodegradation of the active LCK inhibitor 1 upon continuous irradiation with 365 nm stresses the need to utilise caging groups that employ longer wavelengths of light for the photolytic decaging reaction.Given the harmful effects of UV light towards biological samples and its poor tissue penetration, the use of longer wavelengths of light would also impart enhanced biocompatibility.The absorption spectrum of the coumarin caged inhibitor 3d shows strong absorption at 400 nm and a rapid decrease in the absorbance maximum of 3d was observed upon irradiation with 405 nm (ca.27 mW cm −2 , Fig. S4 †).The absorption of the BODIPY caged inhibitor 3e shows two well-dened bands at 384 nm and 531 nm, corresponding to the inhibitor and BODIPY caging group, respectively (Fig. 2).Upon irradiation at 523 nm (ca.8 mW cm −2 ) a rapid decrease at 530 nm was observed.Importantly, photodecomposition of 1 was not observed upon continuous irradiation with 523 nm (Fig. S7 †).
Given the uorescent nature of the coumarin and BODIPY decaged products (f F > 0.07, Table S1 †), the decaging reaction of these caged substrates (3c-e) could also be monitored from the increase in emission arising from the generation of the uorescent decaged product (Fig. S22-S24 †).Due to the weak uorescent properties of 1 in aqueous solution, minimal changes in the emission occurring from the LCK inhibitor at 517 nm was observed upon decaging.From the UV/vis experiments, decaging cross sections of 8 × 10 2 M −1 cm −1 and 4 × 10 2 M −1 cm −1 were determined for 3d and 3e, respectively (Table 1).

IC 50 determination of LCK inhibitor 1 and caged inhibitors 3c-e
As no signicant photodecomposition was observed of the decaged LCK inhibitor 1 during the photoinduced decaging reaction for 3c, 3d and 3e, the inhibitory activity for LCK of these caged substrates and the uncaged inhibitor 1 was assessed using the ADP-Glo™ Kinase Assay from Promega.Under these assay conditions, an IC 50 of 2.4 mM was obtained for compound 1 (Fig. S30 †), while no inhibitory activity against LCK was observed for all caged substrates (Fig. S31-S33 †).This clearly shows that attachment of the selected caging groups efficiently blocks the inhibitory action of inhibitor 1.

Fluorescence titration studies of caged inhibitor 3e with LCK
Previous work demonstrated the solvatochromic properties of LCK inhibitor 1 via uorescence titration experiments, in which a dramatic increase in emission intensity and a blue-shi in the emission maximum were clearly observed in concert with binding to LCK. 25 In order to determine how the inclusion of the caging group on the exocyclic amino moiety of 1 affects these diagnostic changes in uorescence upon binding, additional uorescent titration experiments were performed.As the emission from the BODIPY caging group does not overlap with the emission arising from 1, which allows for discrimination of the uorescence from BODIPY and 1, the caged inhibitor 3e was chosen for this study.The uorescence titration commenced with the addition of aliquots of the BODIPY-caged inhibitor 3e to a solution of the LCK enzyme (1 mM), until a total of 0.5 mM of 3e was added (Fig. 3A).Over the course of the addition, changes in emission maxima and intensity were monitored at both 442 nm (uorescence from inhibitor) and 520 nm (uorescence from BODIPY).The linear nature of the uorescence intensities versus concentration signals that there is no strong specic binding of the caged inhibitor 3e to LCK, and that the BODIPY caging group is preventing the LCK inhibitor from binding to the hydrophobic active site.Aer the titration, the sample was exposed to 523 nm light.This resulted in a dramatic increase in emission intensity at 442 nm and 520 nm, indicating the release and binding of the 'active' LCK inhibitor 1 as well as the release of the uorescent decaged BODIPY product, respectively (Fig. 3B).It is proposed that specic binding of 1 to the ATPbinding site of the LCK enzyme is responsible for the signicant increase in emission at 442 nm.Indeed, inhibitor 1 emits uorescence centred at 517 nm in aqueous solution.However, binding to the hydrophobic pocket of LCK shis the emission maxima to 442 nm, as demonstrated in a prior study. 25n efforts to support that the observed increase in uorescence at 442 nm is due to inhibitor 1 binding to the hydrophobic pocket of LCK, a displacement experiment with the non-uorescent ATP-competitive LCK inhibitor, TC-S7003 (IC 50 = 7 nM) 35 was performed.Upon the addition of TC-S7003 (0-1.0 mM) Fig. 2 Monitoring the decaging reaction of 3e using UV/vis absorption spectroscopy.(top) Absorption spectra of 3e in aqueous solution before irradiation (black) and after irradiation at 523 nm for 180 seconds (red, power z 8 mW cm −2 ); (bottom) changes in absorbance at 530 nm upon irradiation at 523 nm (0-180 seconds).
to the sample containing decaged LCK inhibitor 1, decaged BODIPY S20 and LCK enzyme, a substantial decrease in emission from LCK inhibitor 1 at 442 nm was observed, while minimal changes in emission from the decaged BODIPY product S20 (520 nm) occurred (Fig. 3C).These observations clearly show that uorescence monitoring allows for tracking of the inhibitory action of this compound.The "extreme" spectra are collected in Fig. 4, where it is seen that ratiometric intensity readings can be used to follow both decaging and binding to the enzyme.
As the uorescence quantum yield of 1 is much lower in aqueous solution compared to when bound to the LCK enzyme, the abovementioned observations strongly suggests that 1 binds specically to the enzyme active site upon decaging, and is subsequently displaced by the addition of TC-S7003.Encouraged by these ndings, we undertook further studies in live cells.

Cellular uptake and intracellular decaging of compounds 3c-e in PBMCs
Peripheral blood mononuclear cells (PBMCs) were incubated with caged inhibitors 3c-e.Using a ow cytometry-based method (5-laser BD LSR Fortessa), cells were exposed to light at 355 nm and emission measured at 425-475 nm and 500-530 nm.As depicted in Fig. 5A, all caged inhibitors were taken up by the cells, as cells emitted light at higher intensity when incubated with the caged LCK inhibitors.The concentration dependence of the uorescence intensity shown in Fig. 5A further supports this notion.The caged inhibitors were taken up aer only 5 minutes of incubation (Fig. 5B).Moreover, cell morphology was kept unchanged, indicating no drastic impact on cell viability (Fig. S34 †).
Intracellular decaging was investigated by irradiating cells pre-incubated with the caged inhibitors at 365 nm (100 s), 405 nm (100 s), and 523 nm (350 s) for 3c, 3d, and 3e, respectively.Subsequently, cells were exposed to light at 355 nm for emission readout at 425-475 nm and 500-530 nm, respectively,  using ow cytometry.Irradiation of the cells at the indicated wavelengths indeed resulted in the release of the active LCK inhibitor 1, as the emission intensities at 425-475 nm and 500-530 nm were increased as compared to cells not exposed to decaging light (Fig. 6).

Light-mediated LCK inhibition in NK cell line
NK cells are innate immune cells with an intrinsic capacity to kill target cells upon activation.NK cells are activated via a set of activating receptors that upon binding to ligands on encountered cells induce a signalling cascade that leads to NK cell activation.The release of cytotoxic granules (degranulation) and/or cytokine production occurs as a result of NK cell activation, which ultimately leads to NK cell killing of the target cells.Among the activating receptors is NKG2D, for which the activating signalling cascade requires the presence of LCK kinase. 36o obtain a functional cellular assay where NK cell responses are dependent on LCK inhibition, we made use of a recently described CRISPR-Cas9-modied K562 cell line, in which ligands to key activating NK receptors other than LCKdependent NKG2D were knocked-out. 37These ligands were B7-H6, which binds to NKp30, as well as PVR and Nectin-2, both of which binds to DNAM-1.These triple knock-out (tKO) K562 cells thus become more dependent on NKG2D signalling, and accordingly on the presence of active LCK kinase.
NK cells activated overnight in the presence of IL-2 (500 IU mL −1 ; PeproTech) were incubated with caged LCK inhibitors and either exposed to light using a LED-array (irradiation conditions identical to the ow cytometry experiments previously described, Fig. 6) or kept in the dark.tKO K562 cells, stained with the Cell Trace™ CFSE Cell proliferation kit (Invitrogen), were added to the NK cells, and the cells were subsequently co-incubated in the presence of a CD107a-PE antibody (BD Biosciences) for 3 hours at 37 °C, 5% CO 2 .The CD107a antibody allows for detection of activated degranulating NK cells. 38Cells were also stained with a LIVE/DEAD® Fixable Near IR Dead stain kit (Invitrogen) to be able to determine the viability of the tKO K562 cells aer exposure to NK cells.All analyses were performed using a BD LSR Fortessa SORP ow cytometer.In the absence of tKO K562 cells, the caged inhibitors had no effect on NK cell degranulation.For compounds 3c and 3d, both NK cell degranulation (Fig. 7A) and NK cell lysis of tKO K562 cells (Fig. 7B) were signicantly decreased upon irradiation compared to the non-irradiated caged compounds, clearly demonstrating light-induced activation of these compounds.Surprisingly, irradiation of 3e did not result in any signicant change in NK cell degranulation or tKO K562 cell viability, suggesting that efficient decaging of compound 3e is not occurring within the NK cells.

Fluorescence bioimaging of caged inhibitors 3c-e in NK cells
As a means to visualise cellular distribution, NK cells were incubated with 5 mM solutions of 3c-e and then either irradiated at the respective wavelengths for decaging or kept in the dark before analysis via uorescence microscopy.
Aer incubation and subsequent irradiation with light to initiate the decaging reaction, blue-to-green uorescence  arising from the cytoplasm without any apparent subcellular distribution was observed for compounds 3c and 3d (Fig. S38 and S39 †).In contrast, live 3e-treated NK cells exposed to 523 nm light display green uorescence localised at the cell periphery, pointing to selective accumulation of 3e within the cell membrane (Fig. S40 † and 8A).To further evaluate the subcellular localisation of 3e, NK cells were co-incubated with a cell membrane specic probe (CellMask™ Deep Red) as a counterstain to 3e (Fig. 8B).The large degree of colocalisation of 3e and CellMask™ Deep Red illustrated in Fig. 8C supports the proposed subcellular localisation for 3e and hence reduced internalisation within NK cells.The colocalisation is supported by (i) the Pearson correlation coefficient (PCC) against CellMask™ Deep Red, which was calculated to 0.85 for the whole image (Fig. 8D); and (ii) the good alignment between the emission proles of the two different probes (Fig. 8E).
Colocalisation experiments were also performed with analogues 3c and 3d aer irradiation with light (Fig. S41 and S42 †).The substantial decrease in the PCCs (0.29 and 0.25, respectively) corroborates that the uorescence was non-specically localised within the NK cells and accounts for the efficient uptake of coumarin-caged inhibitors.These results further support the occurrence of the photoinduced release of the LCK inhibitor 1 from compounds 3c and 3d in the subcellular milieu as well as the observed light-mediated cellular activity when employing these caged derivatives.
As expected, NK cells incubated with 3c and 3d and kept in the dark (i.e.no decaging) display emission intensities that were substantially lower compared to those detected in cells that were irradiated with UV light for decaging (Fig. S46-S47 vs. S38-S39 †).Interestingly, this observation does not apply to compound 3e, where the emission levels are similar regardless of whether cells were irradiated with light or kept in the dark (Fig. S48 vs. S40 †).The Corrected Total Cell Fluorescence (CTCF) plot, which summarizes all different explored scenarios (Fig. S55 †), illustrates these ndings.Moreover, the subcellular localisation of all compounds was not affected by the exposure to light.That is, under dark conditions, compounds 3c and 3d were non-specically distributed throughout the cytoplasm, while 3e was entrapped within the cell membrane.This was further corroborated by the visual inspection of the images together with the calculated PCCs against the commercial cell membrane stain (0.31, 0.29, and 0.79 for 3c, 3d, and 3e, respectively; for further details see Fig. S49-S51 †).
The fact that similar emission intensities were observed in both scenarios (with and without irradiation at 523 nm) for 3e further supports the notion that photo-induced decaging of compound 3e is not occurring.The decaging mechanism for BODIPY-derived caging groups is reliant on the presence of water to react with the BODIPY cation that forms as a result of photo-induced heterolytic cleavage. 39Thus, it was anticipated that the accumulation of 3e in the hydrophobic environment of the membrane prevents the release of the LCK inhibitor 1 when irradiated with light.Furthermore, this explains the lack of biological activity for irradiated 3e in the functional cellular assays.This hypothesis can be further supported by recent studies utilising coumarin- [40][41][42] and xanthenium-derived 43 caging groups, which also undergo the same S N 1-type decaging mechanism observed for BODIPY derivatives.These recent studies demonstrate the effect of water content on decaging efficiency, in which higher water content results in increased photolysis quantum yields.Such results suggest that one needs to consider the polarity of the intended environment where photolysis is to be performed.In cases where photolysis is to occur in a hydrophobic environment, caging groups that are not reliant on the presence of water for their decaging mechanism, such as o-nitrobenzyl 44,45 and tertiary coumarin 40 variants, should be considered.
Negative control NK cells, i.e., without any compound treatment, did not show signicant background uorescence  when either irradiated with light or kept in the dark (Fig. S43-S45 and S52-S54 †).

Conclusions
The development of release-and-report LCK inhibitors that exhibit 'OFF-ON' uorescent changes in concert with the release and subsequent binding of the LCK inhibitor to the enzyme are described.This has been achieved through the introduction of photolabile caging groups onto a solvatochromic LCK inhibitor.Fluorescence titration experiments of caged inhibitor 3e with LCK demonstrate that the decaging process can be readily monitored by an increase in emission intensity observed from the caging group, while a diagnostic increase in the emission intensity and a blue-shi of the emission maxima of the 'active' LCK inhibitor report its binding to the LCK enzyme.
Employing a functional assay whereby NK cells are dependent on NKG2D signalling, photo-induced LCK inhibition was investigated.It was observed that the nature of the caging group cellular uptake and subcellular localisation prior to the release of the 'active' LCK inhibitor 1. Coumarin-derived caging groups demonstrated non-specic intracellular localisation and light-dependent LCK inhibition, while the use of a BODIPY-derived caging group resulted in the selective accumulation within the cell membrane and poor photo-induced cellular activity.It is anticipated that the hydrophobic environment of the cell membrane hinders the cellular uptake of 3e, and in turn, the occurrence of efficient decaging within live cells.
Given the need to further our understanding of the role of LCK in both health and disease, it is envisioned that the caged LCK inhibitors will serve as valuable molecular probes to manipulate LCK signalling with high spatiotemporal control.While we have demonstrated the concept of release-and-report inhibitors on kinase enzymes, this approach has the potential to be extended to other biorelevant targets where spatiotemporal control in a cellular setting would be benecial.

Fig. 1
Fig. 1 Working principle of proposed caged inhibitors.Biologically active LCK inhibitor 1 is released by means of light, and only shows strong emission upon binding to LCK enzyme.Different caging groups are incorporated, classifying them as (A) non-fluorescent or (B) fluorescent.

Fig. 3
Fig. 3 Fluorescence titration studies of LCK with BODIPY-derived caged inhibitor 3e.(A) Fluorescence titration of LCK (1 mM) with caged inhibitor 3e in Tris buffer, pH 7.5, (top) emission spectra before (black) and after the addition of 0.5 mM (red) of 3e, employing 350 nm as the excitation wavelength; (bottom) monitoring the changes in fluorescence intensity at 442 nm (black) and 520 nm (red) upon increasing concentration of 3e (0-0.5 mM).(B) (top) emission spectra of 3e (0.5 mM) with LCK (1 mM) in tris buffer, pH 7.5, before irradiation (black) and after irradiation at 523 nm (red), employing 350 nm as the excitation wavelength for emission readout; (bottom) monitoring the changes in fluorescence intensity at 442 nm (black) and 520 nm (red) upon irradiation of caged inhibitor 3e with 523 nm.(C) Displacement fluorescence titration, displacing decaged 1 from the ATP-binding site of LCK with the ATP-competitive inhibitor TC-S7003, (top) emission spectra before (black) and after the addition of 1.0 mM (red) of TC-S7003, employing 350 nm as the excitation wavelength; (bottom) changes in the fluorescence intensity at 442 nm (black) and 520 nm (red) upon increasing of ATP-competitive LCK inhibitor TC-S7003 (0-1.0 mM).

Fig. 4
Fig.4Comparison of emission spectra from fluorescence titration studies of LCK with BODIPY-derived caged inhibitor 3e before irradiation (black), after irradiation (red) with 523 nm where decaged 1 is bound to LCK and after decaged 1 has been displaced from the ATPbinding site (blue).

Fig. 5
Fig. 5 Cellular uptake of caged LCK inhibitors 3c-e.(A) Flow cytometry data show increased emission at wavelengths 425-475 nm and 500-530 nm, upon cellular uptake of caged LCK inhibitor as indicated.(B) Timing of caged LCK inhibitor cellular uptake.Representative flow cytometry data showing cellular uptake of caged 3c after incubation with 5 mL 3c for indicated times.

Fig. 6
Fig. 6 Decaging of caged LCK inhibitors after cellular uptake.Emission at 425-475 or 500-530 nm in lymphocytes that were first incubated with caged LCK inhibitor and subsequently exposed to light at indicated wavelength and time or kept in the dark.Error bars show SD of the fluorescence intensity.

Fig. 7
Fig. 7 NK cell degranulation (A) and frequency of dead tKO K562 cells (B) after 3 h coincubation of NK cells and tKO K562 target cells, in the presence or absence of caged LCK inhibitor (0.5, 1 and 5 mM), with and without light irradiation for decaging.In (A), data were normalized to control with no inhibitor present.Two-way ANOVA, p-values represent impact of irradiation on degranulation (A) or cytotoxicity (B).

Fig. 8
Fig. 8 Fluorescence images of NK cells incubated with (A) 3e upon exposure to 523 nm light (green, l exc = 532 nm; refer to ESI † for details on light treatment before bioimaging), and (B) CellMask™ Deep Red (red, l exc = 633 nm).(C) Colocalization-merged images of 3e and CellMask™ Deep Red.(D) Correlation plot and PCC for 3e and CellMask™ Deep Red images.(E) Emission intensity profile plots along the blue line for the different compounds under study.Scale bar: 5 mm.

Table 1
Spectroscopic data for compound 1 and caged derivatives 4a, 4b and 3c-e in aqueous solution (10% DMSO in H 2 O) a