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Mussel-inspired human gelatin nanocoating for creating biologically adhesive surfaces

Authors Yang X, Zhu L, Tada S, Zhou D, Kitajima T, Isoshima T, Yoshida Y, Nakamura M, Yan W, Ito Y

Received 14 January 2014

Accepted for publication 22 February 2014

Published 29 May 2014 Volume 2014:9(1) Pages 2753—2765

DOI https://doi.org/10.2147/IJN.S60624

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3


Xi Yang,1,2 Liping Zhu,1 Seiichi Tada,1 Di Zhou,3 Takashi Kitajima,1 Takashi Isoshima,1 Yasuhiro Yoshida,1,4 Mariko Nakamura,1,5 Weiqun Yan,2 Yoshihiro Ito1,3

1Nano Medical Engineering Laboratory, RIKEN, Saitama, Japan; 2School of Pharmaceutical Sciences, Jilin University, Jilin, People’s Republic of China; 3Emergent Bioengineering Materials Research Team, RIKEN Center for Emergent Matter Science, Saitama, 4Department of Biomaterials and Bioengineering, Graduate School of Dental Medicine, Hokkaido University, Hokkaido, 5Dental Hygiene Program, Kibi International College, Okayama, Japan

Abstract: Recombinant human gelatin was conjugated with dopamine using carbodiimide as a surface modifier. This dopamine-coupled human gelatin (D-rhG) was characterized by 1H-nuclear magnetic resonance, mass spectroscopy, and circular dichroism. D-rhG-coated surface properties were analyzed by physicochemical methods. Additionally, cell attachment and growth on the modified surfaces was assessed using human umbilical endothelial cells. Binding of gelatin onto titanium was significantly enhanced by dopamine conjugation. The thickness of the D-rhG coating depended on the treatment pH; thicker layers were formed at higher pH values, with a maximum thickness of 30 nm. D-rhG enhanced the binding of collagen-binding vascular endothelial growth factor and cell adhesion as compared with gelatin alone, even at the same surface concentration. The D-rhG surface modifier enhanced substrate binding by creating an adhesive nanointerface that increased specific protein binding and cell attachment.

Keywords: recombinant human gelatin, dopamine, natural catechols, cell adhesion, cell culture, titanium


Introduction

Modification of the surfaces of materials used for cell culture and tissue engineering is often necessary to provide suitable material surface environments for contact with cells and tissues.1,2 Gelatin coating is widely used for surface modification. Gelatin is a mixture of peptides and proteins produced by partial hydrolysis of collagen extracted from the skin, bone, and connective tissue of a number of different animals, including domesticated cattle, chicken, pigs, and fish. However, human gelatin or collagen is required for medical applications.

Therefore, recombinant methods of producing human gelatin or collagen have been recently developed and investigated.3 Olsen et al prepared low molecular weight recombinant human gelatin using yeast,4 Duan et al reported an expression system for hydroxylated gelatin using Pichia pastoris,5 Shoseyov et al developed a technique to generate recombinant human collagen from a genetically engineered tobacco plant,6 and Adachi et al used transgenic silkworms to produce recombinant human gelatin by introducing a type I collagen α1 chain gene that encompassed the entire triple helical region.7

We have modified recombinant human gelatin to expand its functions and applications. For example, gelatin modified with cholesterol was prepared as nanosized gel particles,8,9 and photoreactive gelatin was prepared to covalently immobilize gelatin itself and to coimmobilize other biological molecules on various types of organic materials.10 However, immobilization of gelatin to inorganic materials, which is employed for replacement of hard tissues such as bone, joints, and teeth, remains difficult.11,12

Biomimetic approaches inspired by mussel adhesive activity have recently been devised to modify inorganic materials with biological molecules. Because of its location in the active site of mussel adhesive protein, the importance of the catechol structure of 3,4-dihydroxyphenylalanine (DOPA) has been recognized. Dopamine (3,4-dihydroxyphenethylamine), which has a similar structure, has been used by many researchers as a surface treatment to prepare organic layers, even on inorganic surfaces.1320 Further, dopamine has been attached to synthetic polymers, derivatives of which are used for surface modification of metals.2123 These treatments not only provide organic layers, but also increase immobilization of biological molecules on the surfaces of various materials.2433

Various methods for dopamine conjugation have been investigated, including direct chemical coupling with polysaccharides. Hyaluronic acid, heparin, and β-cyclodextrin have been conjugated with dopamine or DOPA to increase the adhesiveness of the original polysaccharides.3438

To extend its applications, we modified human recombinant gelatin (rhG) using dopamine to create a universal surface modifier that can even be used for metal surfaces. We characterized this molecularly defined, recombinantly prepared biopolymer in detail, and examined its biological adhesiveness using a collagen-binding growth factor39 and human umbilical endothelial cells (HUVECs). Titanium was used as the treated inorganic material because of its widespread application in many biomedical devices.32,33,40,41

Materials and methods

Materials

Proteins

The rhG was produced by transgenic silkworms and purified from their cocoons in the manner described by Adachi et al.7 A fusion protein consisting of the fibronectin collagen binding domain and vascular endothelial growth factor (CBD-VEGF) was prepared as described previously.39

Cells

HUVECs were obtained from Lonza (Basel, Switzerland) and expanded in EGM2 medium (Lonza) containing 5% fetal bovine serum, antibiotics, insulin-like growth factor, ascorbic acid, hydrocortisone, and angiogenic factors, including basic fibroblast growth factor, epidermal growth factor, and vascular endothelial growth factor (VEGF).

Substrates

Titanium-coated glass discs (15 mm in diameter) were prepared as previously reported.40,41

Chemicals

3,4-Dihydroxyphenethylamine hydrochloride (dopamine) and N-hydroxysuccinimide were purchased from Wako Pure Chemical Industries (Osaka, Japan). 1-Ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (water-soluble carbodiimide) was obtained from Dojindo Molecular Technologies, Inc., (Kumamoto, Japan).

Modification of gelatin

rhG was conjugated with dopamine as shown in Figure 1. Lyophilized rhG (350 mg) was dissolved in 60 mL of 2-(N-morpholino)ethanesulfonic acid buffer (50 mM, pH 4.5) and mixed with 150 mg of N-hydroxysuccinimide, 191 mg of water-soluble carbodiimide, and 103 mg of dopamine. The mixture was stirred for 48 hours in the dark at 40°C. The resulting solution was dialyzed against deionized water and lyophilized to obtain a dopamine-conjugated human gelatin (D-rhG). The yield was 206 mg (59%).

Figure 1 Schematic diagram showing the synthesis of dopamine-conjugated recombinant human gelatin.

Surface treatment

The surface of the titanium discs was washed in hexane solution, cleaned with 6 M hydrogen chloride for 10 minutes, rinsed twice with triple distilled water, dried in a vacuum oven for 24 hours, and cleaned photochemically using an Excimer ultraviolet lamp (Ushio Inc., Tokyo, Japan) for 10 minutes before surface treatment, as reported previously.40,41

To treat the surfaces with rhG or D-rhG, each solution was pipetted onto the titanium surface and allowed to stand for 12 hours at 37°C in a moist chamber. Following incubation, the discs were washed three times with phosphate-buffered saline.

Characterization of modified gelatin

1H-nuclear magnetic resonance measurements were performed on a JEOL 400 instrument (JEOL Ltd, Tokyo, Japan). Mass spectroscopy measurements were performed using a QSTAR Elite device (Applied Biosystems, Life Technologies, Carlsbad, CA, USA) for matrix assisted laser desorption/ionization time-of-flight mass spectrometry in the Support Unit for Bio-Materials Analysis Research Resources Center at the RIKEN Brain Science Institute.

Circular dichroism measurements were performed using a J-720 spectrophotometer (Jasco, Tokyo, Japan). Sample volumes of 250 μL (0.01 wt%) were measured using a 1 mm cuvette (scan type, continuous; scan speed, 100 nm per minute; response time, 2.0 sec; bandwidth, 1.0 nm). Each sample was measured twice and average spectra were obtained. Turbidity measurements were performed using 100 μL of sample (0.03 wt%) on a V-550 spectrophotometer (Jasco) at a wavelength of 500 nm.

Surface characterization

The surface atomic composition was analyzed by X-ray photoelectron spectroscopy (AXIS-HS, Kratos, Manchester, UK) under vacuum conditions of less than 10−7 Pa. Al-Kα monochromatic X-rays with a power source of 150 W were used. Scans were acquired at pass energies of 80 eV (wide) and 40 eV (narrow). Overview spectra were obtained in the range of 0–1,100 eV using analyzer pass energies of 80 eV and 40 eV.

Surface wettability was determined by observing the water contact angle on the discs. First, 10 μL droplets of water were placed on the discs (untreated and treated titanium), and images of the droplets were then captured 5 seconds after placement. The water contact angle was measured at 25°C using a contact-angle meter (Kyowa Interface Science Co, Tokyo, Japan). All contact angles were determined by averaging ten different point values measured on each surface.

The thickness of the polymer was measured using an M-2000UI ellipsometer (JA Woollam Co, Lincoln, NE, USA) in the spectral range of 245–1,500 nm at three different incident angles (50°, 60°, and 70°).

The surface morphology of the samples was observed using an MPD-3D atomic force microscope (Asylum Research, Co, Goleta, CA, USA). The images were taken in AC (noncontact) mode using an atomic force microscope tip (NCH-W, NanoWorld AG, Neuchatel, Switzerland) in dry atmospheric pressure conditions.

Binding assay of gelatin

The binding of gelatin to the titanium surface was measured at 25°C using a quartz crystal microbalance with dissipation monitoring (Meiwafosis Co, Tokyo, Japan). First, Milli-Q water (Millipore Corporation, Billerica, MA, USA) was allowed to run until the baseline stabilized. Next, the sample was run for 3 minutes at 65 μL per minute. The pump was then turned off for 15 minutes, after which the substrate was washed in running Milli-Q water. At least three measurements were performed and the average value was calculated.

Growth factor binding assay

The treated titanium discs were incubated with a solution of fusion protein, CBD-VEGF (2 μg/mL, based on the VEGF concentration) for 12 hours at 4°C and then washed with phosphate-buffered saline. The amount of VEGF bound to the gelatin was determined using an anti-VEGF mouse monoclonal antibody (R&D Systems, Minneapolis, MN, USA) as follows. The discs were rinsed with phosphate-buffered saline-Tween (0.2% v/v), blocked in an aqueous solution of nonfat milk (4% w/v) for 30 minutes, washed again three times with phosphate-buffered saline-Tween (0.2% v/v), and incubated with an anti-VEGF antibody (1:500) overnight at 4°C. After incubation with a secondary antibody (anti-mouse IgG) labeled with fluorescein isothiocyanate (GE Healthcare, Little Chalfont, UK) for one hour at room temperature, the surface images were taken on an AxioObserver fluorescent microscope equipped with an AxioCam MRc5 camera (Carl Zeiss Co, Ltd, Göttingen, Germany). The amount of bound CBD-VEGF was measured by AxioVision 4.8 digital image software (Carl Zeiss) on the images of the disc surfaces. To make calibration curves, various known concentrations of the secondary antibody conjugated with fluorescein isothiocyanate were spotted on the surface of titanium and treated similarly.

Cell culture

HUVECs maintained in EGM2 medium at 37°C in 95% humidified air/5% CO2 were recovered by trypsinization and resuspended in fresh medium for the following experiments.

For the cell attachment assay, titanium discs treated with rhG and D-rhG were washed, sterilized with ethanol and phosphate-buffered saline, and placed in 24-well tissue culture plates. The suspension of HUVECs was added to the treated titanium discs and the cells were incubated in EGM2 medium for 30 minutes. After removal of the unattached cells, the number of attached cells was counted under a phase-contrast microscope (CKX 41, Olympus, Tokyo, Japan).

For the cell growth assay, HUVECs were recovered in basal culture medium (EBM2, Lonza) with 1% fetal bovine serum but without angiogenic factors. The cell suspension was added to D-rhG-treated or rhG-treated titanium discs after binding with CBD-VEGF as prepared above. The culture medium was changed every 2 days, and after 5 days of culture, cell proliferation was assessed by a cell counting kit (WST8, Dojindo Molecular Technologies, Inc.) using the method described by Ishiyama et al.42

Statistical analysis

Independent experiments were performed at least three times. Triplicate samples were analyzed in each experiment and representative data are shown. The significance of the data obtained from the control and treated groups was statistically assessed by paired Student’s t-tests, with P-values less than 0.05 considered to be statistically significant.

Results and discussion

Characterization of modified gelatin

The nuclear magnetic resonance spectrum of D-rhG showed benzene ring peaks included in the dopamine at 6–7 ppm (Figure 2). Based on the integration of the peaks, approximately five dopamine groups were conjugated with each rhG. However, the molecular weight of unmodified gelatin was 89,612 Da and that of modified gelatin was 90,634 Da (Figure 3). The difference in the weights (1,022 Da) between the modified and unmodified gelatins corresponded to 6.7 dopamine molecules (152 Da). Both measurements indicate that five or six dopamine groups were conjugated in the D-rhG.

Figure 2 1H nuclear magnetic resonance spectra of (A) rhG and (B) D-rhG.
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

Figure 3 Matrix assisted laser desorption/ionization time-of-flight mass spectra of rhG and D-rhG. The values shown on the left peaks are measured weights.
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

Considering that there are 36 lysine groups in rhG, about 15% of the lysine groups in rhG were used for the conjugation. Circular dichroism spectra showed no significant conformational changes due to dopamine modification (Figure 4).

Figure 4 Circular dichroism spectra of rhG (broken line) and D-rhG (solid line).
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

Modified gelatin solutions

The gelatin solutions are shown in Figure 5. Although the color of unmodified gelatin was the same at all pH values, the color of modified gelatin was pH-dependent. At higher pH values, the color was dark yellow. The turbidity of the D-rhG solution also depended on pH (Figure 6), and was more turbid at higher pH values. Turbidity increased with time, suggesting molecular aggregation in the solution. A dose-dependent turbidity change was also observed as shown in Figure S1, as observed in dopamine solution (Figure S2). The turbidity of the D-rhG solution was saturated in the range of more than 3 mg/mL concentration for all pH conditions, whereas the rhG solution did not show any concentration-dependent change in turbidity in any sample. Surface treatment of modified gelatin was done using 3 mg/mL gelatin solution and the turbidity of the solution correlated with surface binding of D-rhG. These data suggest that incorporation of dopamine and pH-dependent reactivity changes contributed to D-rhG binding to the titanium surface.

Figure 5 Appearance of rhG and D-rhG at different pH values.
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

Figure 6 Turbidity of rhG and D-rhG after 10 minutes (min) and 24 hours at different pH values.
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

These results are similar to previously reported results for dopamine solutions.32,33 It is likely that Michael addition or Schiff base reactions are prevalent in the high-pH dopamine solutions, as reported elsewhere.15 Based on this, we concluded that D-rhG has properties similar to those of dopamine. Although the content of dopamine in D-rhG was not very high, conjugation significantly affected the properties of gelatin.

Surface characterizations of D-rhG-coated titanium

Table 1 shows the results for water contact angle measurements on the treated titanium discs. Treatment with gelatin reduced the hydrophilicity of titanium. Although the effect of rhG was not dependent on pH, the effect of D-rhG was dependent on pH. The water contact angle of the D-rhG treated-surface was highest at pH 8.5, indicating a reduction in surface hydrophilicity.

Table 1 Water contact angle of droplets on rhG-treated or D-rhG-treated titanium surfaces
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

The chemical composition of the treated surfaces was characterized with X-ray photoelectron spectroscopy, as shown in Figure 7, and the results are summarized in Table 2. Bare titanium plate exhibited mainly titanium and oxygen peaks. After treatment with gelatin, a new nitrogen peak appeared and the carbon peak intensity increased, while the peaks for titanium and oxygen were reduced. These results demonstrate the surface coverage of titanium by gelatin. The relative magnitudes indicate that D-rhG covered more of the surface than rhG and that this coverage was pH-dependent, as shown in Table 2. At higher pH values, the area of the surface covered by D-rhG was increased.

Figure 7 X-ray photoelectron wide spectra of titanium treated with (A) rhG and (B) D-rhG.
Note: C1s, N1s, Ti2p, and O1s are orbitals of elements, carbon, nitrogen, titanium, and oxygen, respectively.
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin; Control, non-coated titanium surface.

Table 2 X-ray photoelectron spectroscopic analysis of treated surfaces
Note: C1s, N1s, Ti2p, and O1s are orbitals of elements, carbon, nitrogen, titanium, and oxygen, respectively.
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

The mass of bound rhG and D-rhG was measured by quartz crystal microbalance (Figure 8). Although the binding of D-rhG was almost the same as that of rhG at acidic pH, it was significantly higher than that of rhG at neutral and basic pH values. It is likely that D-rhG, at higher pH values, bound onto the titanium surface and accumulated with the aggregation of D-rhG in solution (Figure 10C).

Figure 8 Binding measurement by quartz crystal microbalance at different pH values. Mean and standard deviation of three experiments. *P<0.05; **P<0.01.
Abbreviations: NS, not significant; rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

Figure 9 Thickness measured by ellipsometry. The means ± standard deviations of three experiments are shown. *P<0.05.
Abbreviations: NS, not significant; rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

Figure 10 Surface morphology measured by atomic force microscopy. (A) rhG at pH 8.5 (scan size 20 μm), (B) D-rhG at pH 7 (scan size 90 μm), and (C) D-rhG at pH 8.5 (scan size 90 μm). The top figure in (C) is the cross-sectional height profile measured at the red line in the morphology image. The bottom figure in (C) is an optical microscope image of D-rhG at pH 8.5 (scale bar 10 μm).
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

This result was also confirmed by thickness measurements using ellipsometry (Figure 9). The measured thicknesses displayed the same order and trends as those calculated from the mass of bound gelatin (Figure 8). The thickness ranged from 5 nm to 30 nm. The thickness of D-rhG layers formed at pH 8.5 was about four times that formed at pH 4.5 and was about six times as thick as rhG formed at pH 8.5.

The surface morphology of the titanium discs treated with rhG or D-rhG was observed by atomic force microscopy (Figure 10). The surfaces of the rhG-treated discs at all pH values (Figure 10A) were as smooth as the nontreated discs. The surface of the discs treated with D-rhG at pH 4.5 and 7.0 (Figure 10B) was also mostly smooth, except for several particle-like structures that were possibly protein aggregates. In contrast, the discs treated with D-rhG at pH 8.5 showed long island structures (Figure 10C). The height of these islands was about 20 nm (top figure of Figure 10C), their width was typically a few microns, and their length was 10–20 μm. These islands were also observable by optical microscopy (bottom figure of Figure 10C). The island structures might be related to the high turbidity of the D-rhG solution at pH 8.5 (Figure 6), suggesting aggregation of the protein molecules. A similar pH dependence was also observed in poly(dopamine) formation.4346

Specific protein binding on D-rhG coated surface

The capture of collagen binding growth factors is important for the specificity of bound gelatin10 and for other tissue engineering applications.4750 Therefore, binding of CBD-VEGF onto the gelatin-treated surface was assessed using the anti-VEGF antibody (Figure 11).

Figure 11 Binding of CBD-VEGF onto treated titanium at different surface concentrations of rhG or D-rhG. The means ± standard deviations of three experiments are shown. *P<0.05; **P<0.01.
Abbreviations: NS, not significant; rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin; CBD-VEGF, collagen binding domain and vascular endothelial growth factor.

Treatment with gelatin increased the binding of CBD-VEGF, with higher amounts of gelatin bound at pH 8.5 than at pH 4.5. This result indicates that modification of gelatin by dopamine did not affect the affinity binding of CBD-VEGF, and that binding was principally dependent on the surface concentration of gelatin. D-rhG enhanced CBD-VEGF binding slightly, but significantly more than rhG at the same surface concentration at pH 4.5. This suggests that conjugated dopamine may affect protein adsorption.

Cell attachment and growth

The effect of immobilized gelatin on cell behavior was examined by incubating HUVECs on the treated surfaces. Figure 12 shows that bound gelatin enhanced cell attachment, with higher cell attachment on surfaces with more bound gelatin. Additionally, a slight increase in cell binding was observed for D-rhG-treated compared with rhG-treated surfaces at the same surface concentration (pH 4.5). Dopamine conjugation may also enhance the attachment of cells, similar to the results obtained for protein binding, where the poly(dopamine)-treated surface was observed to enhance cell adhesion because of the catechol moieties.51

Figure 12 Cell attachment on gelatin-bound titanium surfaces over 30 minutes. The number of human umbilical endothelial cells adhered to the titanium surfaces treated with gelatin at different pH values was counted. The means ± standard deviations of five measurements are shown. *P<0.05; **P<0.01.
Abbreviations: NS, not significant; rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

Figure 13 shows the increase in growth of HUVECs on gelatin-treated titanium discs with CBD-VEGF. Even without CBD-VEGF, cells grew to some extent on the D-rhG-treated and rhG-treated surfaces. The presence of CBD-VEGF captured by gelatin significantly enhanced cell growth. In particular, the surfaces treated with D-rhG at high pH showed remarkable cell growth. In summary, dopamine conjugation enhanced cell attachment to and growth on titanium discs via efficient surface coating, likely due to the catechol moieties51 and the specific affinity binding of growth factor fusion protein.

Figure 13 Cell proliferation on gelatin-treated titanium discs with bound CBD-VEGF. The extent of proliferation was assayed using a cell counting kit (absorbance at 450 nm). The means ± standard deviations of three experiments are shown. *P<0.05; **P<0.01.
Abbreviations: NS, not significant; CBD-VEGF, collagen binding domain and vascular endothelial growth factor.

Conclusion

The binding affinity of human recombinant gelatin to a titanium surface was significantly enhanced by conjugation with dopamine. The bound gelatin directly enhanced cell attachment. The D-rhG-coated surface is suitable for the capture and sequestering of a specific growth factor that supports cell proliferation. We conclude that this mussel-inspired dopamine modification is an effective method for preparation of adhesive materials and the gelatin application described here may be useful for human cell culture systems and other tissue engineering applications.

Acknowledgment

This work was supported in part by a grant from the Japanese Society for Promotion of Science Grants-in-Aid for Scientific Research (22220009).

Disclosure

The authors report no conflicts of interest in this work.


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Supplementary materials

Figure S1 Dose-dependent turbidity of solutions of rhG and D-rhG at different pH values.
Abbreviations: rhG, recombinant human gelatin; D-rhG, dopamine-coupled human gelatin.

Figure S2 Turbidity of dopamine solutions at different concentrations.

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