Intracellular delivery of fluorescent protein into viable wheat microspores using cationic peptides

Microspores are specialized generative cells with haploid genome that demonstrate the amenability toward embryogenesis under certain conditions. The induced microspore culture technique is largely exploited by the breeding programs of wheat and other crops due to its high efficiency for generation of the large number of haploid plants in the relatively short period of time. The ability to produce mature double haploid plant from a single cell has also attracted attention of the plant biotechnologists in the past few years. More importantly, the possibility to deliver proteins for improvement of embryogenesis and the genome modification purposes holds great potential for transgene-free wheat biotechnology. In the present study, we examined the ability of cationic and amphipathic cell penetrating peptides (CPPs) to convey a covalently-linked mCherry protein inside the viable microspores. We demonstrate that the affinity of CPPs to the microspore cells dependents on their charge with the highest efficiency of CPP-mCherry binding to the cells achieved by cationic CPPs (penetratin and R9). Additionally, due to overall negative charge of the microspore cell wall, the successful uptake of the protein cargo by live microspore cells is attained by utilization of a reversible disulfide bond between the R9 CPP and mCherry protein. Overall, the approach proposed herein can be applied by the other biotechnology groups for the fast and efficient screening of the different CPP candidates for their ability to deliver proteins inside the viable plant cells.


Introduction
Bread wheat (Triticum aestivum L.) is one of the major economically important crops worldwide that provides around one fifth of the calories to human population (Wang et al., 2014a). The creation of necessary genetic diversity, introduction of the new traits and the generation of improved cultivars for wheat involves predominantly classical breading. The last, in turn, relies on the techniques which can generate a large number of haploid plants either by pollination of wheat with alien species (Hordeum bulbosum, maize or sorghum) (Barclay, 1975;Laurie and Bennett, 1988a,b) or by microspore and anther culture. Despite some benefits of the wheat pollination technique, the microspore culture produces the large number of haploid plants in the shorter period of time (Touraev et al., 1996;Hul and Kasha, 1997;Hu and Kasha, 1999). More importantly, being a synchronized population of single cells with haploid genome and morphogenic potential, the microspore technique offers enormous prospective for improvement of embryogenesis in the culture as well as the possibility of genome editing at a single-cell level. Substantial effort has been made to develop methods for transformation of microspores and microspore-derived tissue.
Overall, depending on the physiological stage that transformation occurs at, the procedures can be classified as: gametophytic and sporophytic (Resch and Touraev, 2010). Whereas the former one encompasses pollination using either the transformed mature pollen or in vitro cultured pollen grains derived from transformed microspores, the latter one utilizes haploid microspore-derived embryos as the plant material for stable transformation. In most of the cases the transformation is performed using either A. tumefaciens or electroporation or bombardment (Brisibe et al., 2000;Folling and Olesen, 2001;Kumlehn et al., 2006;Chauhan and Khurana, 2011;Brew-Appiah et al., 2013). While being efficient for the introduction of foreign DNA in the wheat genome, unfortunately, neither of these techniques currently offers the possibility of protein delivery into viable microspore cells. Direct introduction of the protein molecules into microspores at the certain physiological stage can potentially be utilized for improvement of the culture embryogenesis and generation of the higher number of green haploid plants for the breeding programs. The broader application includes the exploitation of the designed endonucleases (i.e., Zinc Finger Nucleases, Transcription activator-like effector nucleases, CRISPR/Cas9, and meganucleases) in the form of proteins for the permanent introduction of mutations at the selected loci. Moreover, delivery of the functional enzymes in the form of proteins eliminates the possibility of generating the plants containing transgenes and the resulting product is expected to be void of regulation covering GMO crops (Voytas and Gao, 2014).
An alternative technique for the cargo delivery into live cells has been proposed in the recent years that utilizes the natural ability of cell penetrating peptides (CPPs) to internalize protein, DNA or nanoparticles into animal and plant cells (Chang et al., 2005(Chang et al., , 2014Liu et al., 2013). The first CPP, discovered in 1988, was the domain of transcriptional activator protein (Tat) of the human immunodeficiency virus type 1 (HIV-1) (Frankel and Pabo, 1988;Green and Loewenstein, 1988). Later on, it has been established that the presence of the basic amino acids in the CPP sequence is prerequisite for its translocation through the plasma membrane and accumulation in the cytoplasm and nucleus (Vivès et al., 1997). Subsequently, a number of naturally-occurring and synthetic CPPs were identified with the different properties capable of delivering a wide range of bioactive molecules into the living cells (Fonseca et al., 2009;Huang et al., 2013;Chang et al., 2014;Wang et al., 2014b). Depending on the origin they can be classified as protein-derived, synthetic and chimeric (Lindgren and Langel, 2011). Additionally, based on their physical-chemical properties CPPs can be divided into amphipathic, hydrophobic, and cationic peptides.
The interaction between CPP and the cargos can be either covalent or non-covalent. Whereas, the former one is usually made through disulphide bridges, ester or peptide bonds, the latter one relies on the weak van der Waals forces, electrostatic interactions, and hydrophobic effects (Chang et al., 2014). Previously, we have shown that cationic peptides (Tat and Tat2) are able to deliver protein and DNA molecules in the form of non-covalent complexes into triticale microspores (Chugh et al., 2009). Nevertheless, it still remains vague whether the covalently-linked CPPs can convey the protein molecules in their native state inside the live microspores and how CPPs with different physical-chemical properties interact with the microspore cells. In the present study, we selected two cationic [penetratin (Derossi et al., 1994) and R9 (Futaki, 2002)] and two amphipathic [transportan (Pooga et al., 1998) and model amphipathic peptide (Oehlke et al., 1998)] CPPs and examined their ability to deliver functional covalently-linked mCherry protein into live microspore cells. For this, in-frame fusion of proteins with CPP residues at the N-terminus were purified from bacterial culture and the screening for the best peptide for mCherry conveyance inside the microspore cells was conducted. The data presented in this communication reveals the drastic difference between CPPs for their ability to interact with microspores as well as the importance of utilization of the temporary covalent bonds for the protein cargo internalization inside viable cells.

Plant Cultivation
Wheat seeds (cultivar AC Andrew) were germinated and grown in the Cornell mix as described in Asif et al. (2013) and Sinha and Eudes (2015). The plants were treated with 2.5 ml/l of Tilt ™ (propiconazole, Syngenta) before the tillering stage No. 2 as per (Zadoks et al., 1974) and Intercept ™ (0.004 g/l of soil, Imidacloprid, Bayer) once sufficient root development was established to control pests. The tillers were harvested when the microspores reached mid-to-late uninucleate stage. The tillers were kept at 4 • C for 3 weeks with their bases in distiled water and their heads wrapped in aluminum foil. Following 3 weeks ± 3 days of pre-treatment, the spikes were extracted from their tillers and after evaluation of their general appearance, only the most homogenous spikes were used for microspores isolation.

Microspores Isolation
Isolation of microspores was done as described previously (Asif et al., 2013;Sinha and Eudes, 2015). Briefly, the stage of microspores was verified using a median floret and an acetocarmine staining. Twelve spikes per extraction were surface sterilized with 10% (v/v) bleach (5.25% sodium hypochlorite) for 3 min followed by three washes with sterile double distiled water with constant agitation. Florets were aseptically dissected and transferred to a sterile and refrigerated 110 ml Warring blender cup (VWR International) containing 50 ml of filter sterilized extraction solution at 4 • C (14 mM KNO 3 , 1.76 mM (NH 4 ) 2 SO 4 , 1.47 mM KH 2 PO 4 , 0.56 mM CaCl 2 , 0.38 mM MgSO 4 , 0.1 mM FeSO 4 , 0.1 mM Na 2 EDTA, 0.9 mM MES and 400 mM mannitol, pH 6.5). The florets were blended twice for 7 s at low speed (18,000 rpm). The extract was filtered through 100 µm sterile mesh (VWR International) and the cells were then pelleted by centrifugation (100 g for 5 min at 4 • C) using a swinging bucket rotor (Eppendorf AG, Hamburg, Germany). After removing the supernatant, the pellet was resuspended in 16 ml of icecold extraction solution. Following a second spin (100 g for 5 min at 4 • C), the microspore cells were resuspended in 6 ml of pre-chilled, sterile 20% maltose solution and 1 ml of extraction medium was layered on top. The content was centrifuged at 100 g for 13 min at 4 • C and the viable microspore cells in the interphase were transferred to the fresh 15 ml tube. The microspores were washed again with 15 ml of extraction solution and resuspended to the final concentration of 500 cells per microliter.

Protein Overexpression and Purification from Bacterial Culture
The constructed plasmids were transformed into E.coli strain BL21 (DE3) (Novagen, USA). Single colony of every construct was inoculated into 25 ml of LB (the starter culture) and was grown overnight at 37 • C with shaking at 250 rpm in the presence of 100 µg/ml of carbenicillin. The following day, the starter culture was transferred to 500 ml of LB supplemented with carbenicillin and was grown at 37 • C until OD 600 reached 0.5. The culture was moved to 16 • C and the protein expression was induced with 1 mM IPTG. Following 18 h of protein induction, the bacterial culture was harvested by centrifugation and the pellet was re-suspended in 25 ml of a His-Tag buffer A (20 mM HEPES, 0.3 M NaCl, 5% glycerol and 40 mM imidazole, pH 7.5) supplemented with EDTA-free protease inhibitor cocktail (Roche). Cells were disrupted by sonication (50% intensity, 30 s on, 1 min off time, four cycles, model Q55, Qsonica), and the insoluble debris were removed by centrifugation (18,500 g, 1 h at 4 • C). The clarified supernatant was applied directly onto 1 ml His-Trap column (GE Healthcare Life Sciences) equilibrated with the His-Tag buffer A using an FPLC system (AKTA purifier, GE Healthcare Life Sciences). The elution of bound protein was done using a linear gradient of His-Tag buffer B (20 mM HEPES, 0.3 M NaCl, 5% glycerol and 500 mM imidazole, pH 7.5) from 0 to 100%. Fractions containing the target protein (assessed by the mCherry absorbance at 587 nm) were combined together and concentrated till 0.5 ml using 10K Amicon Ultra-15 spin concentrators (EMD Millipore). The protein was filtered through 0.2 µm low-protein binding filter (EMD Millipore) and loaded onto HiLoad 16/60, Superdex 200 prep grade size exclusion column (SEC, GE Healthcare Life Sciences) primed with SEC buffer (20 mM HEPES, 0.15 M NaCl, pH 7.5) using FPLC system. Following gel filtration step the fractions containing CPP-mCherry protein were analyzed on 10% SDS-PAGE gel. The fractions with more than 90% purity were combined together and concentrated using spin concentrators till at least 50 µM.
Glycerol was added to the fractions till the final concentration of 5% and the proteins were stored at −80 • C.

R9-mCherry Complex Formation
To prepare R9-mCherry complex with the covalent bond through disulfide bridge, purified Cys-mCherry protein (50 µl; 1 nmol in HEPES SEC buffer, pH 7.5) and up to 30 nmol of Cys-(Npys)-(D-Arg) 9 peptide in 50 µl of water (AnaSpec) were combined and allowed to react at room temperature for at least 1 h with no mixing (Liu et al., 2014). The non-covalent complex formation was done by mixing Cys-mCherry protein (50 µl; 1 nmol in HEPES SEC buffer, pH 7.5) and 1 nmol of L-Arg 9 peptide in 50 µl of water (AnaSpec). The solution was incubated for 1 h with no mixing at room temperature.

Microspores Treatments
Microspores were treated either with in-frame fusion or in vitro combined Arg 9 -mCherry protein. Protein solutions (up to 2 nmol in 100 µl) were mixed with 100 µl of microspores (50,000 cells) in extraction buffer and incubated for 1 h (unless otherwise indicated) at room temperature. Following incubation, microspores were washed three times with 2 ml each of extraction buffer to remove the excess of protein. Microspores were resuspended in 200 µl of extraction buffer and fluorescein diacetate (FDA) was added till 2.4 µM in order to visualize viable cells (Sinha and Eudes, 2015). All experiments were done in three biological replicates.
Collecting the Data using Plate Reader and Microscopy Imaging Microspores viability and the level of intensity after treatment with CPP-Cys-mCherry proteins were measured using BioTek Synergy Mx microplate reader (BioTek Instruments, Inc., USA). For this, the microspore solution was resuspended and 12,500 cells in 50 µl volume were pipetted into every well of the black 96-well plate (Costar, Fisher Scientific). For FDA and mCherry measurements, the fluorescent reading was done at excitation/emission wavelengths of 492/517 and 587/610 nm, respectively. The data normalization was done by setting the fluorescent reading from the FDA measurement in the untreated control sample to 100%. For the mCherry signal detection, the reading from untreated control was set to 1 and the fold difference as compared to control was calculated. No crossreading was detected between two fluorescent signals under aforementioned conditions. All measurements were done in three biological and two technical repeats. The visual examination of treated microspores was done using both EVOS FL cell imaging system (Life Technologies) and confocal laser scanning microscope Olympus, FV1000 (Olympus).

Statistical Analysis
The statistical significance was confirmed by single-tailed paired Student's t-test with α = 0.05 and the single factor ANOVA.

Selection of CPPs for In-frame Fusion with mCherry Protein
The mCherry protein was chosen as a cargo due to its stability, fast maturation time, high level of fluorescence, and low auto fluorescence level of microspores in the mCherry spectrum range. Four distinct CPPs were picked up for microspore transfection experiments based on their physicalchemical properties ( Table 1). The nucleotide sequences coding for corresponding CPPs and 6xHis sequence were fused inframe to the coding sequence of mCherry at the 5 ′ -and 3 ′ends, respectively, using PCR. The resulting PCR fragments were cloned into pET45b(+) plasmid (Figures 1A,B). The proteins were purified from bacterial culture with the final purity of more than 98% ( Figure 1C). All mCherry fusions demonstrated same intensity of fluorescence in regard to their concentration indicating that CPPs did not affect the protein confirmation (Supplementary Figure 1). The mCherry protein bearing the cysteine at the N-terminus was used as a no-CPP control treatment for all microspore transfection experiments.

The Interaction of CPP-mCherry Proteins with Microspore Cells
Two cationic (R9 and penetratin) and two amphipathic (transportan and MAP) peptides were used to test their ability to translocate covalently linked mCherry protein into viable microspore cells. Treatment of microspores with equal amounts (1 nmol each) of either Cys-mCherry or CPP-Cys-mCherry proteins for 1 h, followed by examination using fluorescent microscopy, revealed that both cationic CPPs demonstrate the highest binding to the negatively charged microspore's exine as compared to amphipathic ones (Figure 2A). The amphipathic CPP-Cys-mCherry proteins showed interaction with the microspore cell wall that was the lowest among CPP-mCherry fusions tested. Treatment of the cells with the R9-Cys-mCherry protein displayed the highest intensity of fluorescent signal among tested CPP-fusion proteins (Figure 2B, Student's t-test, P < 0.05), hence the R9-fusion protein was selected as the candidate for the further detailed examination of its CPP properties. No decrease in microspore viability was observed for any of the treatments under tested conditions (Figure 2C, Student's t-test, P > 0.05).

Evaluation of the R9-Cys-mCherry Interaction with the Wheat Microspores
Further analysis of the R9-Cys-mCherry binding to the microspore cells demonstrated that the effect was dosedependent ( Figure 3A) and the intensity of fluorescent signal demonstrated linear correlation with the amount of applied protein in a range from 0.25 to 2 nmol ( Figure 3B, R 2 = 0.86). The viability of the treated microspores was not compromised under the treatment conditions ( Figure 3C). The interaction of R9-Cys-mCherry with the cells apparently occurred mostly on the surface of the cells, since as little as 5 min was required for the fluorescent signal to achieve its maximum intensity when  Data are shown as average calculated from three independent repeats with SD. For the data normalization see the Materials and Methods Section. The stars indicate statistically significant difference between connected bars (Student's t-test, single factor ANOVA, α = 0.05; R 2 = 0.86 for treatments displayed in B).
1 nmol of the protein was used (Figure 4A, Student's t-test, P > 0.1). Furthermore, the binding of the protein to the microspore outer surface was temperature-dependent ( Figure 4B), although the microspore viability was significantly compromised when the treatment was performed at 37 • C for 1 h (Figure 4D).

Temporary Covalent Bond between R9 and mCherry is Required for Protein Cargo Delivery into Viable Wheat Microspores
Detailed examination of the microspores treated with R9-Cys-mCherry using confocal laser scanning microscopy revealed that the majority of the protein was trapped on the exine of microspores (Figure 5). We hypothesized that the negative charge of exine (Salter et al., 2002) caused a strong binding of the R9-Cys-mCherry protein to the surface of the cells and supplementing of R9 peptide that can form a reversible covalent bond with the target protein is required for the protein to be internalized inside the cells. Having an additional cysteinyl residue at the N-terminus of the protein allowed us to attach an R9 peptide [Cys (Npys)-(D-Arg) 9 ] through asymmetrical disulfide bond that can be dissociated under reducing conditions inside a cell (Liu et al., 2014). The unreacted CPPs may, apparently, coat Cys-mCherry molecules through electrostatic interaction and, thus, further aid in the translocation of the protein through exine and plasma membrane by making the mCherry protein overall positively charged. Due to the known cytotoxicity of CPPs (Scheller et al., 1999), we first examined the effect of Cys (Npys)-(D-Arg) 9 peptide on the microspore viability. The conjugation reaction was performed for at least 1 h at room temperature as described previously (Liu et al., 2014). The microspore cells demonstrated elevated sensitivity to the tested peptide at the Cys-mCherry to CPP molar ratios higher than 1:1 (Figure 6). Hence, the molar ratio of 1:1 was used for the transfection of microspores [1 nmol of Cys-mCherry protein to 1 nmol of Cys (Npys)-(D-Arg) 9 peptide]. Consistent with our hypothesis, supplementing of D-R9 peptide which was able to form disulfide bridges with the mCherry protein resulted in detection of viable microspores with internalized Cys-mCherry protein as revealed by confocal laser scanning fluorescent microscopy (Figure 5). The Cys-mCherry protein was predominantly localized to the cytoplasm and nucleus of the cells and was excluded from the vacuoles. In contrast, we were not able to detect transfected microspores when noncovalent complex formation was performed using L-R 9 peptide (1 nmol of Cys-mCherry protein to 1 nmol of L-Arg 9 peptide). No fluorescent signal was detected when microspores were FIGURE 4 | The effect of different time and temperature treatments on the binding capacity of the R9-Cys-mCherry protein to the microspore cells (A,B, respectively) and on the microspore viability (C,D). For all experiments the treatment was done with 1 nmol of the R9-Cys-mCherry protein, followed by microspore washing for three times and quantification using BioTek Synergy Mx microplate reader. Data are shown as average calculated from three independent repeats with SD. For the data normalization see the Materials and Methods Section. The stars indicate statistically significant difference as compared to untreated control (Student's t-test, α = 0.05). treated with Cys (Npys)-(D-Arg) 9 peptide alone (data not shown).

Discussion
The ability to deliver proteins into embryogenic cells/tissues holds a great potential both for academic and applied studies. Due to the relatively short half-life of proteins, the necessary effects can be achieved transiently and at a particular stage of the cell development. The possible implications include temporary changing the fate of the tissue development, enhancing the embryogenesis level, and even permanent modification of the plant genome. The last approach has been successfully established in animal cells through delivery of designed endonucleases in the form of proteins using CPPs for the transgene-free genome editing purpose (Liu et al., 2014;Ramakrishna et al., 2014). In both cases, synthetic R9 peptide has been used for the protein translocation. The net positive charge of the cargo molecule seems to be the requirement for successful cellular uptake in the animal cells. For instance, the relatively large protein molecules like Zinc Finger Nucleases (around 45 kDa) that belong to the family of positive supercharged proteins are able to cross the plasma membrane of the animal cells in active form (Gaj et al., 2012;Liu et al., 2015). At the same time, a number of amphipathic CPPs have been ascribed for the animal cells which are characterized by the helical structure and the presence of lysine residues.
In this study, we made an attempt to compare two different classes of CPPs for their ability to interact with the microspore cells and to internalize protein cargo. Consistent with the previous reports, we observed that cationic peptides demonstrate high affinity for the plant cells (Figures 1A,B) (Chang et al., 2005). For instance, previously, it has been reported that either covalent (Chang et al., 2005) or non-covalent (Chang et al., 2007) complexes with either Tat or R9 were able to convey fluorescent proteins inside the onion and tomato roots and epidermal cells. Additionally, in line with our data neither of the treatments had a cytotoxic effect on the wheat microspores when CPPs where permanently fused to the protein ( Figure 1C) (Chang et al., 2005). On the other hand, to our surprise, neither of the amphipathic CPPs demonstrated strong interaction with microspore cells. These data come in the disagreement with the previous report where both cationic (penetratin, Tat 48-60 ) and amphipathic (transportan and MAP) CPPs were tested for their ability to internalize covalently linked, through disulfide bond, pentapeptide cargo (labeled with the 2-amino benzoic acid fluorophore) into animal cells (Hallbrink et al., 2001). Both amphipathic CPPs demonstrated the highest level of uptake by Bowes human melanoma cells. It has been hypothesized that the difference in the efficiency of cargo delivery between the amphipathic and cationic CPPs is due to the ability of the former ones to enter and exit cells more easily since they are in equilibrium over the plasma membrane while the members of the latter class are not (Hallbrink et al., 2001). At the same time, the kinetics of CPP trafficking through the membrane is probably dependent not only on peptides, but also on the membrane area and lipid bilayer composition, and consequently is cell-type specific.
FIGURE 5 | Analysis of mCherry localization in the microspore cells using confocal laser scanning microscopy. Microspores were incubated with either Cys-mCherry, R9-Cys-mCherry or (D-Arg) 9 -Cys-Cys-mCherry complex at 1:1 molar ratio overnight at room temperature. Following incubation, the cells were washed and stained with 2.4 µM FDA to visualize viable microspores. The TxRed and GFP filter sets were used to capture the fluorescent signals from mCherry and FDA, respectively.
The microspore cell is composed of three parts: exine, intine, and protoplast (Tang et al., 2013). The exine of microspores consists of the sporopollenin that is assumed to have phenolics and polyhydroxylated unbranched aliphatics, coupled by ester and ether linkages, which provide this biopolymer with its characteristic resistance to chemical degradation and tolerance to ambient stress conditions (Quilichini et al., 2010). Intine, in turn, is composed of cellulose and pectin. The only access to plasma membrane for the CPP-cargo complex is assumed to be through the single micropore or germ pore (Chugh et al., 2009). The strong binding of cationic CPP-protein fusions like R9-Cys-mCherry and penetratin-Cys-mCherry to the microspore cells is apparently due to high density of negative charges in the sporopollenin matrix that makes it amphiphilic with a strong preference for polar molecules (Salter et al., 2002). This notion is further supported by the positive correlation that we observed between the charge of the proteins used in the current study and the fluorescent signal observed after treatment of microspore cells with CPP-mCherry proteins (R = 0.7). Additionally, the binding of R9-Cys-mCherry protein was relatively fast, dose-, and temperature-dependent (Figures 3, 4) that suggests for the solely physical-chemical interaction with the exine of the microspores. This however, possessed a challenge for the protein molecules internalization, since they were predominantly trapped on the outer layer of the cells (Figure 6). We hypothesized that a reversible covalent bond between R9 and mCherry protein would allow us to bring the cargo molecule to the close proximity of the micropore and through the plasma membrane, but the link will be reduced as soon as it enters the cell to accommodate the protein release inside the cytoplasm. Due to cytotoxicity of examined R9 CPP [Cys (Npys)-(D-Arg) 9 ] for microspore cells in the amount higher than 1 nmol (Figure 6), the complexes with Cys-mCherry were made at the molar ratios of 1:1. Consistent with our hypothesis, incubation with the (D-Arg) 9 -Cys-Cys-mCherry protein conjugates resulted in the cellular uptake of the fluorescent protein by live microspores (Figure 5). The protein was predominantly localized to cytoplasm and nucleus and was excluded from the vacuoles. At the same time we observed that some cells exhibited marked fluorescence as compared to others. This observation is in agreement with the previous report (Chang et al., 2005) and is apparently due to slightly different physiological stage of development of the cells in population. On the other hand, in contrast to other reports on non-covalent R9-mediated protein delivery into roots, we did not observe a detectable mCherry signal inside viable microspore cells when Cys-mCherry was complexed with L-R 9 at 1:1 molar ratio (Chang et al., 2007). This was probably due to the fact that we used almost FIGURE 6 | Evaluation of Cys (Npys)-(D-Arg) 9 cytotoxicity on the microspore cells. The Cys-mCherry-CPP complex formation was done for 1 h in 100 µl volume by combining 1 nmol of the protein with the different amounts of Cys (Npys)-(D-Arg) 9 in indicated molar ratios. Later, 50,000 cells in 100 µl volume were added to the reaction and the solution was incubated for 1 h at room temperature. Following the washing steps, the viability of microspores was quantified using FDA assay and the microplate reader. The data normalization was done by setting the fluorescent reading from the sample treated with the Cys-mCherry alone to 100%. Data are shown as average calculated from three independent repeats with SD. The stars indicate statistically significant difference between connected bars (Student's t-test, single factor ANOVA, α = 0.05, R 2 = 0.64).
30 times lower final concentration of L-R9 in our transfection experiments as compared to the published study. The sensitivity of microspores to R9 CPP did not allow us to test higher amounts of this cationic peptide.
Overall, in this communication we have described an approach that can be applied by other labs for examination of CPPs with different properties for their ability to interact with the totipotent cells like microspores. At the same time, we provide evidence that careful investigation of the internalization properties of any CPP-cargo is needed, due to physiological specificity of the specialized plant cells. The utilization of the reversible covalent bonds to convey cargos into the plant cells with the high negative charge of the outer layer is a preferable approach. Additionally, the same methodology can be further exploited for other cationic CPPs which may demonstrate higher internalization activity at the lower cytotoxicity rate. The implication of CPP technology for nano-cargo delivery into plant cells is still in its infancy, but, we believe, it holds a great potential for applied and basic studies due to its simplicity, high efficiency and an ability to deliver a wide spectrum of bioactive molecules into plant cells.