Fluorescent protein activated silk used in photoelectric conversion

Abstract

A photoelectric device is disclosed. The photoelectric device includes a first electrode, a second electrode, and an electrolyte disposed between the first electrode and the second electrode. The second electrode includes a transparent layer for allowing light to penetrate into the second electrode, an electron transport layer coupled to the transparent layer, and a genetically hybridized fluorescent silk layer as a photo-sensitizer coupled to the electron transport layer.

Claims

1. A photoelectric device, comprising: a first electrically conductive electrode; a second electrically conductive electrode; and an electrolyte disposed between the first electrode and the second electrode, the second electrode including a transparent layer for allowing light to penetrate into the second electrode, an electron transport layer coupled to the transparent layer, and a genetically hybridized fluorescent silk layer coupled to the electron transport layer.

2. The photoelectric device of claim 1, wherein the genetically hybridized fluorescent silk is generated from genetically engineered domesticated silkworms (Bombyx mori), wherein Anderson light localization of silk enhances light coupling between free space and the photoelectric device on broad spectral and angular ranges.

3. The photoelectric device of claim 2, wherein the genetically hybridized fluorescent silk is enhanced green fluorescent protein (eGFP) silk.

4. The photoelectric device of claim 3, wherein the output of the photoelectric device ranges from about 0.5 V to about 0.027 V as a function of irradiation wavelength ranging from about 405 nm to about 633 nm, respectively.

5. The photoelectric device of claim 3, wherein the output of the photoelectric device ranges from about 109 μA to about 0.1 μA as a function of irradiation wavelength ranging from about 405 nm to about 633 nm, respectively.

6. The photoelectric device of claim 2, wherein the genetically hybridized fluorescent silk is mKate2 silk.

7. The photoelectric device of claim 6, wherein the output of the photoelectric device ranges from about 0.462 V to about 0.027 V as a function of irradiation wavelength ranging from about 405 nm to about 633 nm, respectively.

8. The photoelectric device of claim 6, wherein the output of the photoelectric device ranges from about 93.6 μA to about 0.1 μA as a function of irradiation wavelength ranging from about 405 nm to about 633 nm, respectively.

9. The photoelectric device of claim 2, wherein the genetically hybridized fluorescent silk is TiN mKate2 silk.

10. The photoelectric device of claim 9, wherein the output of the photoelectric device ranges from about 0.478 V to about 0.059 V as a function of irradiation wavelength ranging from about 405 nm to about 633 nm, respectively.

11. The photoelectric device of claim 9, wherein the output of the photoelectric device ranges from about 132.4 μA to about 0.2 μA as a function of irradiation wavelength ranging from about 405 nm to about 633 nm, respectively.

12. The photoelectric device of claim 1, wherein the photoelectric device is a solar cell.

13. The photoelectric device of claim 12, wherein a plurality of photoelectric devices are connected in a series manner to generate a voltage multiple.

14. The photoelectric device of claim 13, wherein the first electrode of one photoelectric device of the plurality is coupled to the second electrode of a neighboring photoelectric device of the plurality.

15. The photoelectric device of claim 12, wherein a plurality of photoelectric devices are connected in a parallel manner to generate a current multiple.

16. The photoelectric device of claim 13, wherein the first electrodes of the photoelectric devices of the plurality are coupled to each other and the second electrodes the photoelectric devices of the plurality are coupled to each other.

17. The photoelectric device of claim 1, wherein the photoelectric device is a photodetector.

18. The photoelectric device of claim 1, the transparent layer of the second electrode includes a layer of conductive oxide (TCO).

19. The photoelectric device of claim 18, the TCO layer includes one of Indium tin oxide (ITO), fluorine doped tin oxide (FTO), or a combination thereof.

20. The photoelectric device of claim 1, the first electrode further includes a layer of platinum.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a cross sectional representation of a device according to the present disclosure.

(2) FIG. 2 is an energy diagram showing electron transport mechanism, based on the device of FIG. 1.

(3) FIG. 3 is another schematic showing electron transport based on the device of FIG. 1.

(4) FIG. 4 is a schematic illustration of reactive oxygen species (ROS) generating mKate2 (transgenic) silk cocoons vs. white (wild-type) silk cocoons both under white light and under green light activation.

(5) FIG. 5 is a schematic representing construction of transfer vector p3×P3-EGFP-pFibH-mKate2 for mKate2 silkworm transgenesis.

(6) FIG. 6 is a photograph (left) and fluorescent image (right) of the silk gland for the transgenic mKate2 silkworm larvae at the 3rd day of the 5th instar.

(7) FIG. 7 is a schematic showing a nucleotide sequences of pFibH-NTR and CTR derived from Genebank Accession No. AF226688. pFibH: fibroin heavy chain promoter domain (1124 bp), NTR-1: N-terminal region 1 (142 bp), intron: first intron (871 bp), NTR-2: N-terminal region 2 (417 bp), CTR: Cterminal region (179 bp), PolyA: poly(A) signal region (301 bp), EGFP: enhanced green fluorescent protein gene, mKate2: monomeric far-red fluorescent protein, ITR (BacR, BacL): inverted repeat sequences of piggyBac arms, 3×P3: 3×P3 promoter, and SV40: SV40 polyadenylation signal sequence.

(8) FIGS. 8 and 9 are sequence listings for peptides from mKate2 and sequence alignment of mKate2/Fibroin H-chain fusion recombinant protein amino acid.

(9) FIGS. 10, 11, and 12 include an SEM image of mKate2 silk fibers (FIG. 10); and confocal fluorescence microscopy images of mKate2 silk fibers under green light excitation (FIGS. 11 and 12).

(10) FIG. 13 is a set of photographs and a table showing the results of electrical measurements based on different types of transgenic proteins in silk.

DETAILED DESCRIPTION

(11) For the purposes of promoting an understanding of the principles of the present disclosure, reference will now be made to the embodiments illustrated in the drawings, and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of this disclosure is thereby intended.

(12) In the present disclosure, the term “about” can allow for a degree of variability in a value or range, for example, within 10%, within 5%, or within 1% of a stated value or of a stated limit of a range.

(13) In the present disclosure, the term “substantially” can allow for a degree of variability in a value or range, for example, within 90%, within 95%, or within 99% of a stated value or of a stated limit of a range.

(14) A novel arrangement for converting photonic energy to electrical energy is presented which is friendly to the environment and is biocompatible. Visible light-driven photocatalysis using plasmonics, which relies on the combination of semiconductor photocatalysts with metal nanostructures/nanoparticles, has received consideration attention for solar energy utilization and conversion. Solar photocatalysis has a variety of energy and environmental applications, such as hydrogen generation, carbon dioxide reduction, desalination, disinfection, and water/air purification. However, such approaches are often intrinsically limited for large-scale and mass production. In addition, potentially hazardous and adverse (e.g. carcinogenic and cytotoxic) effects associated with dye material in the dye sensitized solar cells (DSSC), discussed above, have limited widespread utilization for environmental remediation as well as biocompatibility and biodegradability. In this respect, the present disclosure describes utilization of plasmonic photocatalyst-like biological materials in the form of hybridized protein transgenic silk and further translate them into industrially relevant production.

(15) Referring to FIG. 1, a cross sectional view of a device 100 (not drawn to scale) according to the present disclosure is presented. The device 100 includes a first electrode 102 (an anode) which includes a conductive layer 104 and a platinum (Pt) layer 120 (a cathode) atop the conductive layer 104. The conductive layer 104 typically may optionally include a layer of transparent conductive oxide (TCO) such as Indium tin oxide (ITO) or fluorine doped tin oxide (FTO). An electrolyte (e.g., iodide/triiodide solution) 140 is in contact with the first electrode 102. The electrolyte 140 is disposed between the first electrode 102 and a second electrode 152 (an anode) which includes a layer of hybridized protein transgenic silk 160, a layer of an electron transport layer 180 (TiO.sub.2) with bandgap characteristics that allows energized electrons to move from the higher level of proteins to the conduction band of electron transport layer 180, and a conductive layer 200. The electron transport layer 180 can be an ecologically and biologically friendly material such as TiO.sub.2. The conductive layer 200 typically includes a layer of TCO such as ITO or fluorine doped tin oxide (FTO).

(16) When light 101 is shown on the second electrode 152, the fluorescent protein in the layer of hybridized protein transgenic silk 160 becomes energized from their normal ground state to a higher energy level. The molecule of the fluorescent protein in the layer of hybridized protein transgenic silk 160 thus becomes oxidized and a freed electron is thus injected into the conduction band of the electron transport layer 180, thereby allowing a potential at the second electrode 152, where it is collected for powering a load. The electrolyte 140 then donates electrons to the oxidized molecules of the fluorescent protein in the layer of hybridized protein transgenic silk 160 to regenerate the molecules by receiving an electron from the first electrode 102 thus, creating a current when the second electrode 152 (anode) the first electrode 102 (cathode) are connected in a circuit (not shown). The above-described electron-hole generation is depicted in further detail in FIGS. 2 and 3. In particular, when the fluorescent protein molecules in the layer of hybridized protein transgenic silk 160 are irradiated, the molecules are energized from their ground state (i.e., highest occupied molecular orbit—HOMO—to a higher energy state (i.e., lowest unoccupied molecular orbit—LUMO—S*, as described in equation 1 below:
S.fwdarw.S*,  (1)
where S represents the HOMO energy level, and
S* represents the LUMO energy level. The fluorescent protein molecules in the layer of hybridized protein transgenic silk 160 then become oxidized and in doing so release an electron which now has sufficient energy to move from the valence band to the conduction band, as described in equation 2, below:
S*.fwdarw.S.sup.++e.sup.−,  (2)
where S.sup.+ is the oxidized molecule, and
e.sup.− is the energized electron in the conduction band (CB) of the electron transport layer 180. The oxidized dye molecule (S.sup.+) is regenerated by electrons donated from the electrolyte of the electrolyte later 140 (I.sup.−/I.sub.3.sup.−), as shown in equation 3, below:
S.sup.++3/2I.sup.−.fwdarw.S+½I.sub.3.sup.−,  (3)
The electrolyte of the electrolyte layer 140 is then regenerated by donation of electrons from the second electrode 102 (cathode), as described by equation 4, below:
½I.sub.3.sup.−+e.sup.−.fwdarw.3/2I.sup.−  (4)

(17) According to the present disclosure, biological hybridization of far-red fluorescent proteins and some natural proteins (i.e. silk) is disclosed for a new class of genetically encoded photosensitization activated using visible (or solar) light, directly producing selective radical species. As an example, transgenic red fluorescent proteins (RFP) silk can be mass-produced by scalable and continuous manufacturing. Using the polymeric nature of silk, transgenic RFP silk can also be processed into nanomaterials and nanostructures in a variety of forms.

(18) Silk produced by silkworms has extensively been utilized as fabrics and processed into engineered biomaterials due to its various merits of the superior mechanical and optical properties as well as the biocompatibility and biodegradability. According to the present disclosure, genetically engineered domesticated silkworms are used to generate the biomaterial of interest. The transgenes of interests are expressed by germline transformation using the gene splicing method piggyBac, known to a person having ordinary skill in the art. This silkworm transgenesis method yields transformed animals for multiple successive generations and produces recombinant substances in large amounts. Silkworm transgenesis readily produces natural photocatalyst and photosensitizer materials in an eco-friendly manner, minimizing the use of industrial facilities. Regarding ecological hazard, transgenic silkworms are highly unlikely to pose threats to natural ecosystems, because silkworms are dependent on humans for survival and reproduction as a completely domesticated indoor insect.

(19) mKate2, which is a far-red monomeric fluorescent protein, was chosen as one of the transgenic RFP silk. Referring to FIG. 4, a schematic illustration of ROS generating mKate2 (transgenic) silk cocoons vs. white (wild-type) silk cocoons is shown both under white light and under green light activation. When light shines on mKate2 silk, dye molecules become excited from their ground state to a higher energy state, thereby releasing electrons. Oxygen molecules in presence of free electrons go through a reductive reaction (O.sub.2.fwdarw.O.sub.2) thereby generating reactive oxygen species (ROS) of superoxide (O.sub.2.sup..−) radical and singlet molecular oxygen (.sup.1O.sub.2), as shown in FIG. 4. Also shown in FIG. 4 is a spectral output showing mKate2 energy as a function of light wavelength in nm. The AM 1.5 Standard spectrum refers to a standard terrestrial solar spectrum. The green and the red curves presents the absorption spectrum and the fluorescent emission spectrum of mKate2. Thus, mKate2 can be activated by solar light.

(20) Referring to FIG. 5, a schematic representing construction of transfer vector p3×P3-EGFP-pFibH-mKate2 for mKate2 silkworm transgenesis is shown. For hybridization of mKate2 and silk, mKate2 gene is fused with N-terminal and C-terminal domains of the fibroin heavy chain promoter (pFibH); p3×P3-EGFP-pFibH-mKate2 is the constructed transformation vector Referring to FIG. 7, a schematic is provided showing a nucleotide sequences of pFibH-NTR and CTR are derived from Genebank Accession No. AF226688. pFibH: fibroin heavy chain promoter domain (1124 bp), NTR-1: N-terminal region 1 (142 bp), intron: first intron (871 bp), NTR-2: N-terminal region 2 (417 bp), CTR: Cterminal region (179 bp), PolyA: poly(A) signal region (301 bp), EGFP: enhanced green fluorescent protein gene, mKate2: monomeric far-red fluorescent protein, ITR (BacR, BacL): inverted repeat sequences of piggyBac arms, 3×P3: 3×P3 promoter, and SV40: SV40 polyadenylation signal sequence. 3×P3-EGFP is only for screening a large number of G1 broods, because EGFP fluorescent signals are easily monitored in the stemmata and nervous system at early embryonic and larval stages. Referring to FIG. 6, a photograph (left) and a fluorescent image (right) of the silk gland for the transgenic mKate2 silkworm larvae at the 3rd day of the 5th instar. The silk gland of genetically-encoded mKate2 silkworms is fluorescent.

(21) The homogenous production of mKate2 silk results in a mass density of ˜12.6% mKate2/Fibroin H-chain fusion recombinant protein. In FIG. 4, white (wild-type) silk cocoons are not fluorescent, while mKate2-expressing silk cocoons are fluorescent at excitation of λ.sub.ex=543 nm. Referring to FIGS. 8 and 9, shown are sequence listings for peptides from mKate2 and sequence alignment of mKate2/Fibroin H-chain fusion recombinant protein amino acid. The surface morphologies of silk cocoons were imaged using a scanning electron microscopy (SEM) system (FEI Quanta 3D FEG; Oregon, USA) at 10 keV. In exploiting the fluorescence emission of mKate2 silk, we also performed confocal imaging using an Olympus Fluoview FV1000 confocal laser scanning system adapted to an Olympus IX81 inverted microscope with a 20× UPlanSApo water immersion objective (Olympus, Tokyo, Japan). A green laser excitation source (λ.sub.ex=543 nm) was used with a detection bandpass of 600-700 nm. The typical configuration of confocal microscopy can be summarized as follows: confocal aperture size=50 μm (i.e. ˜0.5 airy unit), NA=0.4, and scan speed (pixel dwell time)=10 μs/pixel. 43 image slices were stacked with a slice thickness of 5 μm along the z-axis, covering an area up to ˜1270×1270 μm.sup.2. The three-dimensional (3D) stacked image was also visualized using Imaris 5.0.

(22) Referring to FIGS. 10, 11, and 12, an SEM image of mKate2 silk fibers (FIG. 10); confocal fluorescence microscopy images of mKate2 silk fibers under green light excitation (FIGS. 11 and 12), are provided. Mass density of mKate2/Fibroin H-chain fusion recombinant protein in the transgenic mKate2 silk is estimated to be ˜12.6%.

(23) A similar mechanism is followed in a solar cell application or a photodetector application of the device 100 of FIG. 1. Three different hybridized protein transgenic silk materials were developed. First is eGFP (Enhanced green fluorescent protein) is chosen as the transgenic protein. According to another embodiment, mKate2 is chosen as the transgenic protein. Finally, TiN mKate2 is chosen as the transgenic protein. The result of different irradiation vs. voltage and current generated for these various transgenic proteins is shown in FIG. 13. At 405 nm, the highest V and I values are obtained for TiN mKate2. This may be attributed to the light absorption (<430 nm) of the electrolyte (I.sup.−/I.sub.3.sup.−, iodide/triiodide electrolyte of the electrolyte layer 160).

(24) To obtain the TiN-hybrid transgenic silk, we fed TiN nanopowders to transgenic silkworms. Titanium nitride (TiN) is a hard material with gold-like optical properties, which is commonly used as coatings for various substrates due to its high melting temperature, strong corrosion resistance, and non-toxicity/biocompatibility.

(25) It should also be appreciated that light can be localized in natural silk (silk fibers and silk cocoons) in the same manner of Nobel Prize winner Philip Anderson's theory (also known as Anderson localization). Anderson light localization in irregular or disordered structures allows for light confinement (or trapping) on broad spectral and angular ranges. Thus, natural silk can offer a robust platform for high-efficiency photovoltaic devices. Anderson light localization of silk enhances light coupling between free space and the photoelectric device on broad spectral and substantially all angular ranges.

(26) Those having ordinary skill in the art will recognize that numerous modifications can be made to the specific implementations described above. The implementations should not be limited to the particular limitations described. Other implementations may be possible.