Data on a delivery of biomolecules into Nicothiana benthamiana leaves using different nanoparticles

Nanoparticles (NPs) have a number of unique properties associated with their ultrasmall size and exhibit many advantages compared with existing plant biotechnology platforms for delivery of proteins, RNA and DNA of various sizes into the plant cells (Arruda et al., 2015; Silva et al., 2010; Martin-Ortigosa et al., 2014; Mitter et al., 2017) [1], [2], [3], [4]. The data presented in this article demonstrate a delivery of biomolecules into Nicotiana benthamiana plant leaves using various types of NPs including gold, iron oxide and chitosan NPs and methods of biolistic bombardment and infiltration. The data demonstrate physical characteristics of NPs coated with fluorescently labeled protein and small RNA (size and zeta-potential) and visualization of nanocomplexes delivery into cells of N. benthamiana leaves by fluorescence microscopy.

. The data presented in this article demonstrate a delivery of biomolecules into Nicotiana benthamiana plant leaves using various types of NPs including gold, iron oxide and chitosan NPs and methods of biolistic bombardment and infiltration. The data demonstrate physical characteristics of NPs coated with fluorescently labeled protein and small RNA (size and zeta-potential) and visualization of nanocomplexes delivery into cells of N.  The data demonstrate delivery of the nanocomplexes into N. benthamiana leaves using two different techniques (biolistic bombardment and syringe infiltration) with subsequent visualization of fluorescently labeled biomolecules inside epidermis cells.
The data may be used for development of easy and effective methods of biologically active component delivery to plant cells for different biotechnological applications.

Data
The data presented demonstrate loading capacity of the fluorescently labeled protein (BSA-FITC) and small RNA (tRNA-Cy3) on the surface of the gold, iron oxide and chitosan NPs (Fig. 1) and represent physical characteristics of assembled nanocomplexes built on gold and iron oxide NPs (Table 1, DLS and zeta-potential data). In Fig. 2, the images of plant cells were taken after delivery of nanocomplexes containing the fluorescently labeled BSA and tRNA into N. benthamiana leaves. N. benthamiana has been chosen as a model experimental plant highly convenient for plant biology and microscopy studies [5].
The labeling of BSA with FITC and total tRNA preparation with Cy3 were performed according to the standard protocols as described previously [7,8]. The protein was loaded onto NPs in the buffer (250 мМ NaCl, 15 мМ Tris HCl, pH 8.0). A mixture consisting of BSA-FITC (0.25 μg/ml), the buffer and a suspension of NPs (2 μl) was incubated at room temperature for 30 min under stirring. To load NPs with tRNA-Cy3, a suspension of NPs and RNA solution were mixed and incubated for 30 min at room temperature under stirring. Before further using, obtained nanocomplexes were sonicated.

Nanocomplex characterisation
For DLS analysis assembled nanocomplexes (gold and iron NPs coated with BSA-FITC or tRNA-Cy3) were placed into the Zetasizer Nano ZS 1 cm cell of (Malvern Instruments, UK), and measurements were obtained using the He−Ne laser (633 nm). Curves were fitted using Dispersion Technology Software (DTS) version 5.10.

Nanocomplex delivery into N. benthamiana leaves
Nanocomplexes were delivered into cells of N. benthamiana leaves by particle biolistic bombardment using PDS-1000/He gene gun (Bio-Rad). Obtained nanocomplexes were spread directly onto the carrier and allowed to air-dry at room temperature for about 2 h. The following conditions: rupture disk pressure -900 psi; target distance -9 cm for gold NPs and 6 cm for iron oxide NPs. were used as a standard bombardment protocol for N. benthamiana leaves. Chitosan nanocomplexes after sonication were infiltrated into leaves by syringe from the bottom side of the leaves. Bright-field and fluorescence images were acquired 2 days after delivery using a Axiovert 200 M microscope (Carl Zeiss) equipped with an Plan-Neofluar 10× and 20× objectives. Pictures were taken using ORCA II ERG-2 digital camera (Hamamatsu Photonics, Japan) and AxioVision LE software.  To load NPs with tRNA-Cy3, a suspension of NPs and RNA solution were mixed and incubated for 30 min at room temperature under stirring. Before further using, obtained nanocomplexes were sonicated.