A Ferritin Photochemical Synthesis of Monodispersed Silver Nanoparticles That Possess Antimicrobial Properties

Petrucci, Oscar D.; Hilton, Robert J.; Farrer, Jeffrey K.; Watt, Richard K.

doi:https://doi.org/10.1155/2019/9535708

Journal of Nanomaterials

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Abstract Introduction Materials and Methods Results Conclusions Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2019 | Article ID 9535708 | https://doi.org/10.1155/2019/9535708

A Ferritin Photochemical Synthesis of Monodispersed Silver Nanoparticles That Possess Antimicrobial Properties

Oscar D. Petrucci,¹Robert J. Hilton,¹Jeffrey K. Farrer,¹and Richard K. Watt¹

Academic Editor: Haisheng Qian

Received31 Aug 2018

Revised01 Nov 2018

Accepted11 Nov 2018

Published06 Feb 2019

Abstract

We previously reported that ferritin acts as a photocatalyst to form monodispersed gold nanoparticles. Because silver possesses a favorable reduction potential (+0.80 V), we postulated that the ferritin photochemical method could be used to reduce Ag(I) to Ag(0). Additionally, we postulated that similar to gold, the reduced silver should nucleate and form silver nanoparticles (AgNPs) on the external surface of ferritin. This study reports that Ag(I) can function as an electron acceptor to form monodispersed AgNPs using the ferritin photocatalytic method. The formation and growth of the AgNPs were monitored by following the surface plasmon resonance (SPR) peak at 420 nm by spectrophotometry. The resulting monodispersed AgNPs were analyzed by transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), and energy-dispersive X-ray spectroscopy (EDX). Gel filtration chromatography demonstrated that the AgNPs comigrated with ferritin through the column suggesting a strong association with ferritin. AgNPs are known to possess antimicrobial properties. The antimicrobial properties of Ferritin-AgNPs were compared to commercially available AgNPs by testing the minimal growth inhibition of Staphylococcus aureus. Commercially available AgNPs inhibited bacterial growth at 5 ppm AgNPs, and Ferritin-AgNPs inhibited growth at 20 ppm Ferritin-AgNPs.

1. Introduction

Silver nanoparticles have unique properties that differ from the bulk material and also differ from the individual atoms or ions [1–8]. The interesting properties of nanoparticles include quantum confinement effects and catalytic properties related to strained atoms or ions on the surface of the nanoparticle. Nanoparticles have been used for a variety of purposes and include catalysts, biosensing, nanoelectronics, drug deliver, and antimicrobial treatments [9].

A variety of characteristics govern the properties of the nanoparticles and depend on the size, shape, and stability of the nanoparticles [10–13]. Capping agents are often used to control the size, shape, and stability of the nanoparticles, but capping agents also influence the properties of the resulting nanoparticles [14–16]. Since many nanoparticles are synthesized for used in biological applications, the use of nontoxic biocompatible capping agents has become an important priority in the synthesis of nanoparticles. Additionally, reducing agents used to prepare nanoparticles are expensive and can be toxic in the environment [7]. Therefore, green synthetic methods for preparing and stabilizing nanoparticles are an important priority. To identify capping and reducing agents that are biocompatible, nanoparticles have been synthesized in the presence of organic matter or fruit extracts to identify biocompatible capping agents [17–20].

Silver nanoparticles (AgNPs) possess many of the interesting nanoparticle properties discussed above, but the susceptibility of AgNPs to oxidative corrosion and aggregation has limited their use in many applications [21]. To overcome these problems, several groups have attempted to synthesize AgNPs inside hollow protein nanocages such as ferritin [21–25]. The theory is that the protein nanocage will replace the capping agents and protect the AgNPs from oxidation but will still allow the nanoparticles to retain their unique properties.

Ferritin is a large spherical protein measuring 12 nm in diameter with an 8 nm hollow interior occupied by a ferrihydrite core (FeOOH) that possesses semiconductor properties [26–30]. This protein, with or without its iron cargo, has been used as a scaffold for forming metal nanoparticles on both the inside and outside by a variety of techniques [31]. Early research focused on depositing metal oxides on the interior of ferritin as a size-constrained reactor to form nanoparticles with a tight size distribution by replacing iron with other metals [32]. Later studies produced elemental forms of the metals inside ferritin by using powerful reducing agents [22, 33]. Ferritin has also been used as a scaffold for the formation of metal nanoparticles on the external surface of ferritin [34–36].

Several groups have synthesized AgNPs inside ferritin [21–25]. Early studies used molecular biology to engineer the ferritin interior to possess silver-binding peptides or thiols to enhance silver accumulation inside ferritin [22, 23]. The bacterial ferritin from Pyrococcus furiosus was shown to possess unique silver-binding domains that bound and allowed the encapsulation AgNPs [25]. Other groups demonstrated the synthesis of size-controlled 1 nm or 4 nm diameter AgNPs inside ferritin [21] or demonstrated that the AgNPs deposited inside ferritin were catalytically active and increasing the rate of iron oxidation [24].

Recently, the photochemical methods for nanoparticle synthesis have been described and included using ferritin as a charge separation catalyst to oxidize organic acids and channel the liberated electrons to reduce metal ions in the solution [28–30, 35–37]. The photochemical reaction is represented in Scheme 1 and outlines one proposed reaction mechanism for forming AgNPs.

The ferritin photocatalyst functions because light can excite electrons from the valence band into the conduction band of the ferrihydrite semiconductor allowing ferritin to act as a charge separation catalyst [28]. The excited electrons are donated to target ions that bind to nucleation sites on the ferritin exterior surface, and the excited electrons are transferred through the redox active protein shell of ferritin [38], or by Fe(II) reduction and release from ferritin [39], to reduce these metal ions to the elemental form. To replenish the electron holes created by the charge separation event, ferritin is able to oxidize sacrificial electron donors present in the solution. Typically, citrate or oxalate is used as the electron donors in these reactions. This reaction allows a photochemical reduction of the metal ions without harsh reducing agents or byproducts and uses ferritin as the capping agent. The resulting AgNP product is associated with the external surface of ferritin so parts of the AgNP are “capped” and stabilized by ferritin. However, the AgNP surface is partially exposed allowing more solvent access than an AgNP completely encapsulated inside ferritin. This synthesis may mimic the work done by Zhai et al. where they deposited AgNPs on the surface of silica spheres to stabilize the AgNPs but preserve the nanoparticle catalytic properties [40]. Ferritin synthesized with other metal nanoparticles encapsulated inside ferritin are also capable of performing the photochemical charge separation reactions [41–45]. We chose to test the surface reactivity of the Ferritin-AgNPs (Ftn-AgNPs) by analyzing the antimicrobial activity of these nanoparticles.

Metal nanoparticles have antimicrobial activity [46, 47]. AgNPs have antimicrobial properties but generally have very low toxicity to humans so they have been used in topical crèmes and to treat burn wounds [7, 48, 49]. Additionally, AgNPs and AuNPs have been deposited on the surfaces of medical devices and in consumer products as disinfectants [8, 49, 50]. The toxicity to bacteria is caused by the binding of Ag⁺ ions or AgNPs to the sulfhydryl groups, blocking respiration or generating reactive oxygen species (ROS). Additionally, the charge and nature of the capping agents has also been shown to contribute to bacterial toxicity. We desired to test the Ftn-AgNPs for their ability to inhibit bacterial growth as an evaluation of the reactivity of the AgNPs bound on the surface of ferritin.

This work describes the successful photoreduction of silver ions to form silver nanoparticles (AgNPs) on the surface of ferritin, using the ferritin photocatalytic reaction system. The synthesis reaction uses ferritin, citrate, and light to photoreduce Ag(I) ions to Ag(0) so the reaction has no hazardous reactants or products. The novelty is the photochemical reaction that drives the AgNP synthesis. The AgNP samples were characterized by UV-visible spectrophotometry, transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), and energy-dispersive X-ray spectroscopy (EDX). Size exclusion chromatography was used to confirm that the AgNPs are attached to the external surface of the ferritin protein. Finally, we report that Ferritin-AgNPs possess antimicrobial activity against Staphylococcus aureus.

2. Materials and Methods

We obtained the native horse spleen ferritin (Ftn) and silver chloride from Sigma-Aldrich. Ferritin protein concentrations were determined by the Lowry method [51]. The iron content of the native ferritin was 1800 Fe/Ftn as determined by the dithionite/bipyridyl method [38]. The silver nanoparticles (AgNPs) were formed in a solution containing Ftn (150 μg/mL) with TRIS buffer at pH 7.4 (20 mM), sodium citrate (30 mM), AgNO₃ (800 μM), and NaCl (50 mM). The temperature of the samples during illumination was maintained at 25°C using a water-jacketed cuvette holder connected to a temperature-controlled water bath in an Agilent 8453 UV-Vis spectrophotometer. 1 mL samples were placed in a quartz cuvette and exposed to a full spectrum Hg-halide floodlight (Integrated Dispensing Solutions Inc.), and the reaction progression was monitored in the 200-1100 nm range in kinetic mode for the length of the reaction in a UV-Vis spectrophotometer (Agilent 8453). AgNPs were formed and monitored at 420 nm during an 800-second irradiation time. The appearance and size of the NPs were evaluated and visualized by transmission electron microscopy (TEM) performed on a Tecnai F30 operating at 300 kV and by scanning electron microscopy (STEM) and energy-dispersive X-ray spectroscopy (EDX) on a Tecnai F20 operating at 200 kV. The preparation of the samples for TEM was performed using the method described by Petrucci et al. [36]. Size exclusion chromatography was performed with a Superdex 200 10/300 GL column (GE Healthcare Life Sciences, cat. 17-5175-01) by injecting 0.5 mL of freshly prepared AgNPs or 0.5 mL of 150 μg/mL Ftn. Control reactions were conducted in the dark or without ferritin.

2.1. Bacterial Growth Minimal Inhibitory Concentration Test

Fifteen sterile culture tubes were prepared by adding 1 mL of tryptic soy broth (TSB) containing colony-forming units (CFU) of Staphylococcus aureus (ATCC 6538). Then 1 mL of a solution containing Ferritin-AgNPs (at 80, 40, 20, 10, 5, 2.5, or 1.25, 0.625 parts per million (ppm) silver) or commercial AgNPs (American Biotech Labs, at 10, 5, 2.5, or 1.25, 0.625 ppm) was added to each culture. The two remaining tubes, one containing only 2 mL of TSB and one containing 2 mL of TSB plus CFU of S. aureus, were used as experimental controls. The experiment was performed in triplicates.

3. Results

The photocatalytic formation of the AgNPs was monitored by following the change in absorbance at 420 nm which corresponds to the surface plasmon resonance band of AgNPs (Figures 1(a) and 1(b)) [52]. A visible color change from colorless to amber, characteristic of silver nanoparticles in aqueous solution, was observed and provides further evidence supporting the conclusion that AgNPs were successfully synthesized by this method (Figure 1(c)). Control reactions conducted in the dark, as well as in the light but without ferritin, were not able to produce AgNPs.

(a)

(b)

(c)

After illumination the samples were placed on TEM grids and analyzed by TEM and STEM. Two populations of particles were observed, very dense particles and diffuse particles (Figure 2(a)). We hypothesized that the darker particles were AgNPs and that the lighter particles were the iron core of ferritin. The increased atomic density of AgNPs gives a better contrast than the iron cores of ferritin (Figure 2(a)). The dark and light particles were analyzed by STEM using the elemental analysis capability of EDX (Figure 3). In box 1, the electron beam was focused on two light particles, and in box 2, the electron beam was focused on two dark particles. The EDX analysis confirmed the diffuse particles (box 1) was iron and the dense particles (box 2) was silver (Figure 3). The size of the AgNPs is uniform with diameters of (Figure 2(b); calculated from 126 AgNPs).

(a)

(b)

(a)

(b)

(c)

To determine if the AgNPs were attached to or possessed a strong association with ferritin, the sample was passed over a gel filtration column to determine if the AgNPs comigrated with ferritin or if they could be separated from ferritin. A ferritin standard was passed over the column, and the elution was detected by monitoring the ferritin protein at 280 nm (Figure 4). Note that ferritin exists as monomers and as dimers and produces two peaks when passed over a gel filtration column [53]. The sample containing AgNPs and ferritin had a similar two-peak 280 nm elution profile for ferritin monomers and dimers, but the sample eluted much earlier than the ferritin control. This indicates an increase in the ferritin cross-sectional diameter consistent with AgNPs bound on the ferritin exterior surface. Additionally, the elution of AgNPs was monitored following the 420 nm absorbance that corresponds AgNPs. The AgNPs elution peak (~8 min) corresponds to the ferritin dimer peak indicating that AgNPs coelute with ferritin. Remarkably, the AgNPs appear to preferentially associate with ferritin dimers or may cause an increase in ferritin dimerization. This is consistent with the changes in peak height between the ferritin control and the Ferritin-AgNP (Ftn-AuNP) sample. The peaks corresponding to monomers and dimers in the control ferritin sample are found in an almost 1 : 1 ratio, but the dimer peak in the Ftn-AgNP sample is about double that of the monomer peak.

Figure 4

Size exclusion chromatography of the ferritin AgNP solution. A standard of ferritin was passed over the column, and the elution profile was monitored at 280 nm (red). Ferritin runs as a dimer and monomer so it has two peaks. A sample of AgNPs synthesized photochemically by ferritin was passed over the column, and the absorbance was monitored at 280 nm (detecting the protein) and 420 nm (detecting the AgNP plasmon resonance). The AgNPs (420 nm peak, blue) and the ferritin (280 nm peak, green) coelute (~8 min) and are significantly shifted to an earlier elution than the ferritin standard (red), indicating that the particles are attached to the external surface of the protein shell. The presence of AgNPs also appears to shift the ferritin into the dimer species. Note: the absorbance dropping below zero is due to the changes of buffer composition compared to the blank.

We propose the AgNPs associate with ferritin by the following interactions. First, the Ag(I) ions bind to the ferritin shell and are reduced to Ag(0) to start the nucleation of the AgNP on the exterior surface of ferritin (see Scheme 1). Continued illumination facilitates additional Ag(I) reduction to Ag(0) to allow AgNP growth. The AgNPs appear to grow to about 5 nm and then stop growing, but the reason of why growth termination occurs has not been determined. We postulate that the citrate caps the majority of the AgNP surface and the association between ferritin and the AgNPs is through ferritin lysine residues with positive charge and the citrate cap of the AgNP with negative charge.

AgNPs are known for their potent antimicrobial properties [7, 48, 54]; for this reason, we performed a minimal inhibitory concentration test using Ftn-AgNPs to inhibit the growth of Staphylococcus aureus. This would allow us to determine if AgNPs associated on the exterior surface of ferritin retained antimicrobial activity. For an experimental positive control for AgNP antimicrobial activity, we used a commercially available 10 ppm water solution of 5 nm diameter AgNPs to compare with the same size Ftn-AgNPs produced by the ferritin photochemical method. Figure 5 shows that the Ftn-AgNPs inhibit growth at 20 parts per million AgNPs. In contrast, commercial AgNPs inhibit at 5 parts per million. These results were consistent in all three triplicate samples. Although the Ftn-AgNPs are effective at inhibiting the growth of S. aureus, they are about 4-fold less effective than commercial AgNPs. It is possible that the interaction with ferritin blocks some of the surface of the AgNPs and prevents some of the available surface area for inhibiting the bacterial growth. The control tubes containing bacteria without antimicrobial agents or no bacteria showed growth or no growth, respectively.

The literature shows that metal NPs have their maximal antimicrobial reactivity in the 1-7 nm range, depending on the material. Our nanoparticles are in the 5 nm range, which explains why their antimicrobial activity is comparable to the commercial AgNP standard. The slight decrease in activity (less than 1 log unit) is seemingly due to the interference/stabilization of the AgNPs by the ferritin.

4. Conclusions

The purpose of this research was threefold: (1) to test whether the ferritin photocatalytic method could produce AgNPs, (2) to test if the AgNPs remained associated on the exterior surface of ferritin, and (3) to determine if ferritin AgNPs possessed antimicrobial properties even if part of the AgNP surface was passivated by ferritin. This work demonstrates that we were able to photochemically synthesize ~4 nm diameter monodispersed AgNPs that remained associated on the surface of ferritin. Additionally, the resulting Ftn-AgNP solution possesses antimicrobial activity at a low ppm concentration range.

Finally, we suggest that the biocompatible reagents used to prepare the Ftn-AgNPs, particularly the absence of harsh reagents or surfactants, might allow the Ftn-AgNPs to be used as a mild topical disinfectant. In fact, the combined antimicrobial and iron-sequestering abilities (iron is an essential nutrient for all microorganisms [55, 56]) of the Ftn-AgNPs might represent an effective combined treatment to prevent the growth of human pathogens.

Data Availability

The kinetic, TEM, gel filtration, and bacterial growth inhibition data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Acknowledgments

Funding was provided by Brigham Young University through the Department of Chemistry and Biochemistry.

References

K. M. M. Abou El-Nour, A. Eftaiha, A. Al-Warthan, and R. A. A. Ammar, “Synthesis and applications of silver nanoparticles,” Arabian Journal of Chemistry, vol. 3, no. 3, pp. 135–140, 2010.
View at: Publisher Site | Google Scholar
S. Marin, G. Vlasceanu, R. Tiplea et al., “Applications and toxicity of silver nanoparticles: a recent review,” Current Topics in Medicinal Chemistry, vol. 15, no. 16, pp. 1596–1604, 2015.
View at: Publisher Site | Google Scholar
L. Z. Flores-Lopez, H. Espinoza-Gomez, and R. Somanathan, “Silver nanoparticles: electron transfer, reactive oxygen species, oxidative stress, beneficial and toxicological effects. Mini review,” Journal of Applied Toxicology, vol. 39, no. 1, pp. 16–26, 2018.
View at: Publisher Site | Google Scholar
V. De Matteis, M. Cascione, C. Toma, and S. Leporatti, “Silver nanoparticles: synthetic routes, in vitro toxicity and theranostic applications for cancer disease,” Nanomaterials, vol. 8, no. 5, 2018.
View at: Publisher Site | Google Scholar
C. You, C. Han, X. Wang et al., “The progress of silver nanoparticles in the antibacterial mechanism, clinical application and cytotoxicity,” Molecular Biology Reports, vol. 39, no. 9, pp. 9193–9201, 2012.
View at: Publisher Site | Google Scholar
B. Mahyad, S. Janfaza, and E. S. Hosseini, “Bio-nano hybrid materials based on bacteriorhodopsin: potential applications and future strategies,” Advances in Colloid and Interface Science, vol. 225, pp. 194–202, 2015.
View at: Publisher Site | Google Scholar
K. Mijnendonckx, N. Leys, J. Mahillon, S. Silver, and R. van Houdt, “Antimicrobial silver: uses, toxicity and potential for resistance,” Biometals, vol. 26, no. 4, pp. 609–621, 2013.
View at: Publisher Site | Google Scholar
T. Faunce and A. Watal, “Nanosilver and global public health: international regulatory issues,” Nanomedicine, vol. 5, no. 4, pp. 617–632, 2010.
View at: Publisher Site | Google Scholar
A. S. M. Iftekhar Uddin, D.-T. Phan, and G.-S. Chung, “Low temperature acetylene gas sensor based on Ag nanoparticles-loaded ZnO-reduced graphene oxide hybrid,” Sensors and Actuators B: Chemical, vol. 207, pp. 362–369, 2015.
View at: Publisher Site | Google Scholar
J. Zeng, Y. Zheng, M. Rycenga et al., “Controlling the shapes of silver nanocrystals with different capping agents,” Journal of the American Chemical Society, vol. 132, no. 25, pp. 8552-8553, 2010.
View at: Publisher Site | Google Scholar
C. Xue, G. S. Métraux, J. E. Millstone, and C. A. Mirkin, “Mechanistic study of photomediated triangular silver nanoprism growth,” Journal of the American Chemical Society, vol. 130, no. 26, pp. 8337–8344, 2008.
View at: Publisher Site | Google Scholar
E. Ye, M. D. Regulacio, S. Y. Zhang, X. J. Loh, and M. Y. Han, “Anisotropically branched metal nanostructures,” Chemical Society Reviews, vol. 44, no. 17, pp. 6001–6017, 2015.
View at: Publisher Site | Google Scholar
S. Y. Tee, E. Ye, P. H. Pan et al., “Fabrication of bimetallic Cu/Au nanotubes and their sensitive, selective, reproducible and reusable electrochemical sensing of glucose,” Nanoscale, vol. 7, no. 25, pp. 11190–11198, 2015.
View at: Publisher Site | Google Scholar
M. Green, N. Allsop, G. Wakefield, P. J. Dobson, and J. L. Hutchison, “Trialkylphosphine oxide/amine stabilised silver nanocrystals—the importance of steric factors and Lewis basicity in capping agents,” Journal of Materials Chemistry, vol. 12, no. 9, pp. 2671–2674, 2002.
View at: Publisher Site | Google Scholar
S. S. Shankar, A. Rai, A. Ahmad, and M. Sastry, “Controlling the optical properties of lemongrass extract synthesized gold nanotriangles and potential application in infrared-absorbing optical coatings,” Chemistry of Materials, vol. 17, no. 3, pp. 566–572, 2005.
View at: Publisher Site | Google Scholar
J. S. Lee, A. K. R. Lytton-Jean, S. J. Hurst, and C. A. Mirkin, “Silver nanoparticle-oligonucleotide conjugates based on DNA with triple cyclic disulfide moieties,” Nano Letters, vol. 7, no. 7, pp. 2112–2115, 2007.
View at: Publisher Site | Google Scholar
D. P. Stankus, S. E. Lohse, J. E. Hutchison, and J. A. Nason, “Interactions between natural organic matter and gold nanoparticles stabilized with different organic capping agents,” Environmental Science & Technology, vol. 45, no. 8, pp. 3238–3244, 2011.
View at: Publisher Site | Google Scholar
R. S. R. Isaac, G. Sakthivel, and C. Murthy, “Green synthesis of gold and silver nanoparticles using Averrhoa bilimbi fruit extract,” Journal of Nanotechnology, vol. 2013, Article ID 906592, 6 pages, 2013.
View at: Publisher Site | Google Scholar
S. S. Shankar, A. Rai, A. Ahmad, and M. Sastry, “Rapid synthesis of Au, Ag, and bimetallic Au core–Ag shell nanoparticles using Neem (Azadirachta indica) leaf broth,” Journal of Colloid and Interface Science, vol. 275, no. 2, pp. 496–502, 2004.
View at: Publisher Site | Google Scholar
D. P. Yang, X. Liu, C. P. Teng et al., “Unexpected formation of gold nanoflowers by a green synthesis method as agents for a safe and effective photothermal therapy,” Nanoscale, vol. 9, no. 41, pp. 15753–15759, 2017.
View at: Publisher Site | Google Scholar
J. M. Domínguez-Vera, N. Gálvez, P. Sánchez et al., “Size-controlled water-soluble ag nanoparticles,” European Journal of Inorganic Chemistry, vol. 2007, no. 30, pp. 4823–4826, 2007.
View at: Publisher Site | Google Scholar
C. A. Butts, J. Swift, S. G. Kang et al., “Directing noble metal ion chemistry within a designed ferritin protein,” Biochemistry, vol. 47, no. 48, pp. 12729–12739, 2008.
View at: Publisher Site | Google Scholar
R. M. Kramer, C. Li, D. C. Carter, M. O. Stone, and R. R. Naik, “Engineered protein cages for nanomaterial synthesis,” Journal of the American Chemical Society, vol. 126, no. 41, pp. 13282–13286, 2004.
View at: Publisher Site | Google Scholar
A. Sennuga, J. van Marwijk, and C. G. Whiteley, “Multiple fold increase in activity of ferroxidase-apoferritin complex by silver and gold nanoparticles,” Nanomedicine, vol. 9, no. 2, pp. 185–193, 2013.
View at: Publisher Site | Google Scholar
O. Kasyutich, A. Ilari, A. Fiorillo, D. Tatchev, A. Hoell, and P. Ceci, “Silver ion incorporation and nanoparticle formation inside the cavity of Pyrococcus furiosus ferritin: structural and size-distribution analyses,” Journal of the American Chemical Society, vol. 132, no. 10, pp. 3621–3627, 2010.
View at: Publisher Site | Google Scholar
R. R. Crichton and J. P. Declercq, “X-ray structures of ferritins and related proteins,” Biochimica et Biophysica Acta (BBA) - General Subjects, vol. 1800, no. 8, pp. 706–718, 2010.
View at: Publisher Site | Google Scholar
R. K. Watt, O. D. Petrucci, and T. Smith, “Ferritin as a model for developing 3rd generation nano architecture organic/inorganic hybrid photo catalysts for energy conversion,” Catalysis Science & Technology, vol. 3, no. 12, pp. 3103–3110, 2013.
View at: Publisher Site | Google Scholar
V. V. Nikandrov, C. K. Grätzel, J. E. Moser, and M. Grätzel, “Light induced redox reactions involving mammalian ferritin as photocatalyst,” Journal of Photochemistry and Photobiology B: Biology, vol. 41, no. 1-2, pp. 83–89, 1997.
View at: Publisher Site | Google Scholar
D. Ensign, M. Young, and T. Douglas, “Photocatalytic synthesis of copper colloids from CuII by the ferrihydrite core of ferritin,” Inorganic Chemistry, vol. 43, no. 11, pp. 3441–3446, 2004.
View at: Publisher Site | Google Scholar
I. Kim, H. A. Hosein, D. R. Strongin, and T. Douglas, “Photochemical reactivity of ferritin for Cr(VI) reduction,” Chemistry of Materials, vol. 14, no. 11, pp. 4874–4879, 2002.
View at: Publisher Site | Google Scholar
D. He and J. Marles-Wright, “Ferritin family proteins and their use in bionanotechnology,” New Biotechnology, vol. 32, no. 6, pp. 651–657, 2015.
View at: Publisher Site | Google Scholar
M. Uchida, S. Kang, C. Reichhardt, K. Harlen, and T. Douglas, “The ferritin superfamily: supramolecular templates for materials synthesis,” Biochimica et Biophysica Acta (BBA) - General Subjects, vol. 1800, no. 8, pp. 834–845, 2010.
View at: Publisher Site | Google Scholar
I. Yamashita, K. Iwahori, and S. Kumagai, “Ferritin in the field of nanodevices,” Biochimica et Biophysica Acta (BBA) - General Subjects, vol. 1800, no. 8, pp. 846–857, 2010.
View at: Publisher Site | Google Scholar
L. Zhang, J. Swift, C. A. Butts, V. Yerubandi, and I. J. Dmochowski, “Structure and activity of apoferritin-stabilized gold nanoparticles,” Journal of Inorganic Biochemistry, vol. 101, no. 11-12, pp. 1719–1729, 2007.
View at: Publisher Site | Google Scholar
J. D. Keyes, R. J. Hilton, J. Farrer, and R. K. Watt, “Ferritin as a photocatalyst and scaffold for gold nanoparticle synthesis,” Journal of Nanoparticle Research, vol. 13, no. 6, pp. 2563–2575, 2011.
View at: Publisher Site | Google Scholar
O. D. Petrucci, D. C. Buck, J. K. Farrer, and R. K. Watt, “A ferritin mediated photochemical method to synthesize biocompatible catalytically active gold nanoparticles: size control synthesis for small (~2 nm), medium (~7 nm) or large (~17 nm) nanoparticles,” RSC Advances, vol. 4, no. 7, pp. 3472–3481, 2014.
View at: Publisher Site | Google Scholar
F. Zhang, C. L. Zhang, H. Y. Peng, H. P. Cong, and H. S. Qian, “Near-infrared photocatalytic upconversion nanoparticles/TiO₂ nanofibers assembled in large scale by electrospinning,” Particle & Particle Systems Characterization, vol. 33, no. 5, pp. 248–253, 2016.
View at: Publisher Site | Google Scholar
R. K. Watt, R. B. Frankel, and G. D. Watt, “Redox reactions of apo mammalian ferritin,” Biochemistry, vol. 31, no. 40, pp. 9673–9679, 1992.
View at: Publisher Site | Google Scholar
N. Saenz, M. Sánchez, N. Gálvez, F. Carmona, P. Arosio, and J. M. Dominguez-Vera, “Insights on the (auto)photocatalysis of ferritin,” Inorganic Chemistry, vol. 55, no. 12, pp. 6047–6050, 2016.
View at: Publisher Site | Google Scholar
H. J. Zhai, D. W. Sun, and H. S. Wang, “Catalytic properties of silica/silver nanocomposites,” Journal of Nanoscience and Nanotechnology, vol. 6, no. 7, pp. 1968–1972, 2006.
View at: Publisher Site | Google Scholar
J. S. Colton, S. D. Erickson, T. J. Smith, and R. K. Watt, “Sensitive detection of surface- and size-dependent direct and indirect band gap transitions in ferritin,” Nanotechnology, vol. 25, no. 13, article 135703, 2014.
View at: Publisher Site | Google Scholar
T. J. Smith, S. D. Erickson, C. M. Orozco et al., “Tuning the band gap of ferritin nanoparticles by co-depositing Iron with halides or Oxo-anions,” Journal of Materials Chemistry A, vol. 2, no. 48, pp. 20782–20788, 2014.
View at: Publisher Site | Google Scholar
S. D. Erickson, T. J. Smith, L. M. Moses, R. K. Watt, and J. S. Colton, “Non-native Co-, Mn-, and Ti-oxyhydroxide nanocrystals in ferritin for high efficiency solar energy conversion,” Nanotechnology, vol. 26, no. 1, article 015703, 2015.
View at: Publisher Site | Google Scholar
C. R. Olsen, J. S. Embley, K. R. Hansen et al., “Tuning Ferritin’s band gap through mixed metal oxide nanoparticle formation,” Nanotechnology, vol. 28, no. 19, article 195604, 2017.
View at: Publisher Site | Google Scholar
K. R. Hansen, J. R. Peterson, A. Perego et al., “Lead sulfide quantum dots inside ferritin: synthesis and application to photovoltaics,” Applied Nanoscience, vol. 8, no. 7, pp. 1687–1699, 2018.
View at: Publisher Site | Google Scholar
G.-X. Tong, F. F. du, Y. Liang et al., “Polymorphous ZnO complex architectures: selective synthesis, mechanism, surface area and Zn-polar plane-codetermining antibacterial activity,” Journal of Materials Chemistry B, vol. 1, no. 4, pp. 454–463, 2013.
View at: Publisher Site | Google Scholar
G. Tong, F. du, W. Wu, R. Wu, F. Liu, and Y. Liang, “Enhanced reactive oxygen species (ROS) yields and antibacterial activity of spongy ZnO/ZnFe₂O₄ hybrid micro-hexahedra selectively synthesized through a versatile glucose-engineered co-precipitation/annealing process,” Journal of Materials Chemistry B, vol. 1, no. 20, pp. 2647–2657, 2013.
View at: Publisher Site | Google Scholar
J. S. Kim, E. Kuk, K. N. Yu et al., “Antimicrobial effects of silver nanoparticles,” Nanomedicine, vol. 3, no. 1, pp. 95–101, 2007.
View at: Publisher Site | Google Scholar
K. W. Lem, A. Choudhury, A. A. Lakhani et al., “Use of nanosilver in consumer products,” Recent Patents on Nanotechnology, vol. 6, no. 1, pp. 60–72, 2012.
View at: Publisher Site | Google Scholar
C. P. Teng, T. Zhou, E. Ye et al., “Effective targeted photothermal ablation of multidrug resistant bacteria and their biofilms with NIR-absorbing gold nanocrosses,” Advanced Healthcare Materials, vol. 5, no. 16, pp. 2122–2130, 2016.
View at: Publisher Site | Google Scholar
O. H. Lowry, N. J. Rosebrough, A. L. Farr, and R. J. Randall, “Protein measurement with the folin phenol reagent,” Journal of Biological Chemistry, vol. 193, no. 1, pp. 265–275, 1951.
View at: Google Scholar
S. Pattanayak, A. Priyam, and P. Paik, “Facile tuning of plasmon bands in hollow silver nanoshells using mild reductant and mild stabilizer,” Dalton Transactions, vol. 42, no. 29, pp. 10597–10607, 2013.
View at: Publisher Site | Google Scholar
D. N. Petsev, B. R. Thomas, S. T. Yau, and P. G. Vekilov, “Interactions and aggregation of apoferritin molecules in solution: effects of added electrolytes,” Biophysical Journal, vol. 78, no. 4, pp. 2060–2069, 2000.
View at: Publisher Site | Google Scholar
W. R. Li, X. B. Xie, Q. S. Shi, H. Y. Zeng, Y. S. OU-Yang, and Y. B. Chen, “Antibacterial activity and mechanism of silver nanoparticles on Escherichia coli,” Applied Microbiology and Biotechnology, vol. 85, no. 4, pp. 1115–1122, 2010.
View at: Publisher Site | Google Scholar
M. Caza and J. W. Kronstad, “Shared and distinct mechanisms of iron acquisition by bacterial and fungal pathogens of humans,” Frontiers in Cellular and Infection Microbiology, vol. 3, p. 80, 2013.
View at: Publisher Site | Google Scholar
E. Deriu, J. Z. Liu, M. Pezeshki et al., “Probiotic bacteria reduce salmonella typhimurium intestinal colonization by competing for iron,” Cell Host & Microbe, vol. 14, no. 1, pp. 26–37, 2013.
View at: Publisher Site | Google Scholar

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Copyright © 2019 Oscar D. Petrucci et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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