Open Access

Alternative moth-eye nanostructures: antireflective properties and composition of dimpled corneal nanocoatings in silk-moth ancestors

Journal of Nanobiotechnology201715:61

Received: 29 June 2017

Accepted: 29 August 2017

Published: 6 September 2017


Moth-eye nanostructures are a well-known example of biological antireflective surfaces formed by pseudoregular arrays of nipples and are often used as a template for biomimetic materials. Here, we provide morphological characterization of corneal nanostructures of moths from the Bombycidae family, including strains of domesticated Bombyx mori silk-moth, its wild ancestor Bombyx mandarina, and a more distantly related Apatelodes torrefacta. We find high diversification of the nanostructures and strong antireflective properties they provide. Curiously, the nano-dimple pattern of B. mandarina is found to reduce reflectance as efficiently as the nanopillars of A. torrefacta. Access to genome sequence of Bombyx further permitted us to pinpoint corneal proteins, likely contributing to formation of the antireflective nanocoatings. These findings open the door to bioengineering of nanostructures with novel properties, as well as invite industry to expand traditional moth-eye nanocoatings with the alternative ones described here.


Moth-eye structures Antireflective nanocoatings Biomimetic materials Silkmoth


Moth-eye nanostructures—pseudo-regular arrays of nanopillars first described on corneal surfaces of the nocturnal moth Spodoptera eridania [1]—served as a paradigm for bio-inspired antireflective coating with broad technological applications, from solar cells to art paintings [25]. Gradually matching the refractive index of air to that of the lens material, these nanostructures minimize light reflectance and maximize perception. While physics of the anti-reflectance by nanopillar arrays is well-understood, permitting reliable simulations [6, 7], nature also designed other types of corneal nanocoatings [8], of which some were shown to play the antireflective function too [9, 10]. Numerous studies on artificial nanocoatings showed that the shape, dimensions, as well as the packing order of the nanostructures contribute to the anti-reflectivity [1114].

Model insect organisms, permitting genetic manipulations and/or providing complete information on their genome sequences, have been instrumental in advancing the research on insect molecular, developmental, and cell biology [15]. Following our research on the corneal nanocoatings in Drosophila melanogaster [16, 17], we are now turning to another famous model insect—the silkmoth Bombyx mori.

More than 1000 different B. mori silkworm strains exist worldwide, having different phenotypic and genomic features [18, 19]. The silkworm was domesticated in East Asia from wild B. mandarina moths some 5000 years ago, losing several features essential in the wild habitat on the expense of maximizing silk production [20]. Bombyx moths’ genomes have been fully sequenced [18, 19], increasing their importance as genetic model organisms. While many aspects of the Bombyx biology have been analyzed, these insects have not been previously studied in terms of their corneal morphology and properties. We hypothesized that distinct corneal nanocoatings may be found in the wild vs. domesticated silkmoths.

Results and discussion

To explore differences between corneal nanocoatings in wild and domestic silkmoths, an atomic-force microscopy (AFM) analysis has been performed, comparing the corneal surfaces of B. mandarina, to the samples from two different B. mori strains obtained from Japan (Jp) and Vietnam (Vn, see “Materials and methods”; Fig. 1a–c). Unusually for Lepidopterans, different species of which so far have displayed different varieties of nanopillars, in some species fused into mazes or parallel strands [8], corneal surfaces of B. mandarina reveal a clear nano-dimpled pattern (Fig. 1d), previously described in insects of other orders, such as earwigs or Carabidae beetles [8]. Curiously, corneae of the two B. mori strains reveal different degrees of corruption of this pattern, with the Vn strain depicting a dimple-to-maze transition previously seen in other insects (e.g. bug from Pyrrhocoridae family [8]), and the Jp strain—a complete degeneration into sporadic irregularities (Fig. 1e–h). Fourier analysis [16, 21, 22] confirms this visual inspection, indicating that the B. mandarina and B. mori [Vn] corneal structures are close to quasi-random, while the B. mori [Jp]—to completely random structures (Additional file 1: Figure S1). Fully random structures are known to show less anti-reflectance than the quasi-random structures [11, 12], such as those we see in B. mandarina and B. mori [Vn] (Additional file 1: Figure S1). As B. mori [Jp] corneae further possess randomization in the broadness and depth of the nanostructures (Fig. 1), we may expect even stronger loss of the anti-reflectivity. Using finite-difference time domain-based approximations of the Maxwell function, simulations of the reflectance pattern of structured surfaces were found to match the results received in the process of the optical experiments [6, 7, 23, 24]. However, such simulations in general do not predict antireflective properties of nanostructures, whose dimensions are below 30–50 nm [7, 25], such as those we see in the Bombyx species.
Fig. 1

Corneal nanocoatings in Bombyx moths. ac Photographs of B. mandarina (a), B. mori from Vietnam (b) and B. mori from Japan (c). df Representative AFM scans (5 × 5 µm) of corneal surfaces of the Bombyx species presented in ac. The height dimension of the surface (in nm) is indicated by the color scale next to (f) with the mean set to zero. g, h Calculation of the height of protrusions (from the lowest point up to the next highest point (g) and their broadness (h) of B. mandarina (in red), B. mori [Vn] (in orange), and B. mori [Jp] (in green); n = 50

Given these uncertainties, we decided to directly measure reflectivity from corneal surfaces of the Bombyx moths. This analysis reveals strong reduction of the reflected light in the broad visible spectrum from the dimpled corneal surfaces of B. mandarina and the dimple-to-maze surfaces of B. mori [Vn], as compared to the irregularly rough surface of B. mori [Jp] (Fig. 2). Remarkably, the antireflective properties provided by the Bombyx nano-dimpled coating even exceeded those provided by the nano-pillar arrays of another Bombycidae moth, Apatelodes torrefacta (Fig. 2d, e). While the nano-dimpled B. mandarina arrays (as the nano-pillar A. torrefacta arrays) appear to provide uniform broadband anti-reflectivity, the dimple-to-maze B. mori [Vn] structures are efficient at low wavelengths and start to decrease anti-reflectivity at >650 nm (Fig. 2e). With the theoretical assessment of these findings currently missing, we are left to speculate that either the lack of uniformity in the overall morphology of the dimple-to-maze nanostructures (Figs. 1e, 2b), or their on average smaller dimensions (Fig. 1g, h) could be the cause of this difference of B. mori [Vn] from its wild ancestor. Our findings provide the first demonstration of the antireflective capacity of nano-dimpled surfaces less than 100 nm in depth, indicating that nature has found a relatively low-cost and unpredicted solution to the anti-reflectance.
Fig. 2

Antireflective function of corneal nanocoatings from Bombycidae moths. ad 3D AFM representation (3 × 3 µm) of corneal nanocoatings of B. mori [Jp] (a), B. mori [Vn] (b), B. mandarina (c) and A. torrefacta (d). e Ratio of the experimentally measured reflection spectra to the average reflectance of B. mori [Jp] measured for B. mori [Jp] (green), B. mori [Vn] (orange), B. mandarina (red) and A. torrefacta (gray). Data present as mean ± SD, n = 3 (for the experimental data for B. mori [Vn] n = 2)

Corneal nanostructures are built from proteins and lipids placed on the chitin background [26, 27]. The Turing reaction–diffusion model was proposed to govern the formation and diversity of the insect corneal nanostructures [8], which predicts corneal protein(s) to serve as the key slow-diffusing component of this reaction and the building blocks of the resulting structures. To prove directly that corneal proteins are important for formation of the antireflective nanocoatings, we treated corneae of B. mandarina with a detergent (see “Materials and methods”), and analyzed the resulting samples for their morphology and anti-reflectance. Remarkably, we find that removal of proteins purges away the nano-dimpled coatings (Additional file 2: Figure S2), correlating with a strong loss of the anti-reflective potential of the corneal surface (Additional file 2: Figure S2b). These features, together with the detailed inspection of the remnant nanostructures’ height and broadness (Additional file 2: Figure S2c, d), indicate that protein extraction brings the surface of B. mandarina close to that of B. mori [Jp]. These findings prompted us to pinpoint corneal proteins, which may show differential abundance in the wild vs. the domesticated Bombyx moths.

The choice of B. mori and B. mandarina insects for our analysis was to a large extent dictated by the fact that genomes of these insects have been fully sequenced [18, 19], opening the possibility to identify corneal proteins involved in formation of the nanocoatings—the task not achievable for many other insects (such as A. torrefacta) whose genomes have not been sequenced. Thus, we analyzed the protein samples obtained by the detergent extraction (Additional file 2: Figure S2a) of B. mori and B. mandarina, as well as samples from their underlying retina, by SDS-PAGE followed by mass-spectrometry identification of the most prominent corneal-specific bands (Fig. 3a). This proteomic analysis identified a number of cuticular proteins (CPs, Additional file 3: Table S1), such as CPRs (classical CPs with the chitin-binding domain), and CPHs (hypothetical CPs) [28]. Various chitin-binding domains, RR motifs (where RR2 mediates association with the hard cuticle such as head capsule, and RR1—with soft intermediate membranes), and 18 amino acid repeats can be distinguished in CPs [28].
Fig. 3

Cuticular proteins in Bombyx genus members and the model for nanocoating formation. a SDS-PAGE of samples from cornea and retina of B. mori [Jp] and B. mandarina. Major protein bands unique for cornea (marked by red arrowheads) were MS-identified (see Additional file 3: Table S1). b The percentage of major cuticular proteins in corneal material from B. mori [Jp], B. mori [Vn] and B. mandarina. ce Model of step-wise acquisition of nanostructures on the corneal surface of B. mori from Japan (c), B. mori from Vietnam (d), and B. mandarina (e)

The major proteins, comprising each >10% and together ca. 50% of the total corneal load in B. mandarina corneae, are CPR83, CPR150, CPR19 and CPH30. Remarkably, we find substantial reduction of these proteins in the domesticated moth B. mori [Jp] (Fig. 3a, b). CPR83, CPR150, and CPR19 are the regular CPRs containing the chitin-binding domain 4, whereas CPH30 does not contain a chitin-binding domain but has the 18-residue repeats [29]. CPR83 contains an RR2, while CPR150 and CPR19—the RR1 motifs, and thus may mediate interactions with different types of cuticle [28]. Analysis of the corneal proteome of B. mori [Vn] revealed similar to B. mandarina levels of CPR83 and CPH30, but significantly lower levels of the RR1-family proteins CPR150 and CPR19 (Fig. 3b).

We hypothesize that these changes in the corneal CPs, seen among different Bombyx specimen, underlie the differences in the nanostructures that decorate corneae of these strains. Specifically, we propose that the hard-cuticle binding CPR83, possessing the RR2 motif, and the 18-residue repeat-containing CPH30 are the first proteins to be “gained” in B. mori [Vn] as compared to B. mori [Jp], providing structuring on the corneal surface and strong anti-reflectance (Fig. 3c, d). Next, the soft material-interacting RR1 motif is “recruited” in the form of the CPR19 and CPR150 in corneae of B. mandarina, mediating formation of the well-formed nano-dimpled coatings (Fig. 3e). Genetic manipulations (loss-of-function and overexpression) of these proteins in B. mori or another insect model is required for the unambiguous testing of our hypothesis, and will be subject of future investigations.

Identification of the candidate proteins governing formation of the Bombyx corneal nanocoatings permits creation of novel nanocoatings. Indeed, cloning of the genes encoding for these proteins and their targeted mis- and over-expression in other hosts, such as the genetic model insect Drosophila melanogaster [16, 30] is expected to produce novel corneal nanocoatings—potentially with improved physical properties such as anti-reflectance, self-cleaning, anti-bacterial, etc. Together with the similar analysis of the protein composition of corneal nanostructures in other arthropods, this approach opens the door to a high-throughput bioengineering of nanocoatings, which may eventually lead to generation of nanostructures with features interesting for industrial applications.

In regard to the interest for industry, we wish to stress that the nano-dimpled moth-eye nanostructures we have described here display unexpectedly good anti-reflective properties. Given the high cost of industrial generation of the nano-pillar coatings and their sensitivity to physical damage, these nano-dimpled coatings may represent an attractive industrial alternative, given the low cost fabrication of nanohole surfaces [31].

Materials and methods

The samples of Bombyx mori (p50 strain) and Bombyx mandarina (Oki line) were provided by the National Bio-Resource Project (NBRP) of the Ministry of Education, Science, Sports and Culture of Japan. Additionally, we studied Vietnamese B. mori obtained from the Cuong Hoan Silk Factory, Trung Vuong, Lam Dong Province, Vietnam. The samples of Apatelodes torrefacta (mature adults from Louisiana, USA) were obtained from the online shop

Preparation and analysis of corneal and retinal samples: Corneal and retinal samples were prepared by cutting off the eyes with a scalpel from the heads of mature adult guillotined Bombycidae moths. The retinal material was removed from the immobilized samples into a drop of water by washing and very gentle scrupulous scratching. Upon the separation, the corneal material was further washed 3 times in water. The corneal and retinal samples were extracted from the material of 10 eyes. The samples were boiled for 60 min in the Sample Buffer (62.5 mM Tris–HCl pH 6.8; 10% glycerol; 2% SDS; 1% β-mercaptoethanol; trace of bromophenol blue) prior to separation by 15% SDS-PAGE (Fig. 3) or AFM and reflectance measurement (Additional file 2: Figure S2). Ratio of bands to total protein were counted by the ImageJ software.

Mass-spectrometry (MS): in-gel trypsin digestion and MS were performed by the Protein Analysis Facility of University of Lausanne (Switzerland). The Scaffold viewer software was used for the data analysis with the following parameters: protein threshold 90%, minimum of number of peptides 1, peptide threshold 90%, minimum of probability 90%. The amount of cuticular proteins was counted by using the following formula:
$$\frac{{\mathop \sum \nolimits \left( {\frac{a}{b} \times 100 \times c} \right)_{n} }}{{\mathop \sum \nolimits \left( {\mathop \sum \nolimits \left( {\frac{a}{b} \times 100 \times c} \right)_{n} } \right)_{m} }} \times 100,$$
where a is the percentage of total spectra from protein of interest (particular CP) in one band, b is the percentage of total spectra of all proteins in one band, c is the ratio of band to total protein in the gel, n is the number of bands, and m is the number of CPs.

The corneal samples of B. mori from Vietnam, due to scarceness of material, were directly sent to MS and the results were analyzed as the ratio of the percentage of the total spectra from protein of interest (particular CP) to the percentage of the total spectra of all CPs.

For AFM, corneal samples prepared as described above were attached to a coverslip by a double-sided bonding tape. Microscopy was performed by the NTegra-Prima microscopes (NT-MDT, Zelenograd, Russia) using the contact procedure with the long NSG 11 cantilever (NT-MDT) and the BioScope Resolve, Bruker, with cantilever SCANASYST-AIR. The Gwyddion software [32] was used for visualization and for Fourier analysis.

The same samples were also used for the reflectance measurements, using the JASCO MSV-370 micro-spectrophotometer in the reflection geometry. Using a non-dispersive Schwarzschild-objective and an aperture, the region of interest was set to an area of 300 × 300 µm. The spectral region from beginning of visible spectrum (400 nm) to near infrared (750 nm). The data is used to visualize the spectral ratio \(\left( {{{{\text{R}}_{{\left( {\text{of interest}} \right)}} } \mathord{\left/ {\vphantom {{{\text{R}}_{{\left( {\text{of interest}} \right)}} } {{\text{R}}_{{\left( {B. \, mori\,\,\left[ {\text{Jp}} \right]} \right)}} }}} \right. \kern-0pt} {{\text{R}}_{{\left( {B. \, mori\,\,\left[ {\text{Jp}} \right]} \right)}} }}} \right)\) between the two species.



atomic-force microscopy


cuticular proteins




Authors’ contributions

MK, JL, JS, VC, AB and MF performed the experiments, MK and VLK wrote the manuscript, VLK supervised the research. All authors read and approved the final manuscript.


We thank Prof. Yutaka Banno for providing the B. mandarina and B. mori (p50 strain) samples.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

All data generated or analyzed during this study are included in this published article (and its additional files).

Consent for publication

Not applicable.

Ethics approval

Not applicable.

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Authors’ Affiliations

Department of Pharmacology and Toxicology, University of Lausanne
Department of Materials, ETH Zurich
School of Biomedicine, Far Eastern Federal University


  1. Bernhard CG, Miller WH. A corneal nipple pattern in insect compound eyes. Acta Physiol Scand. 1962;56:385–6.View ArticleGoogle Scholar
  2. Cai JG, Qi LM. Recent advances in antireflective surfaces based on nanostructure arrays. Mater Horiz. 2015;2:37–53.View ArticleGoogle Scholar
  3. Raut HK, Ganesh VA, Nair AS, Ramakrishna S. Anti-reflective coatings: a critical, in-depth review. Energy Environ Sci. 2011;4:3779–804.View ArticleGoogle Scholar
  4. Han ZW, Wang Z, Feng XM, Li B, Mu ZZ, Zhang JQ, Niu SC, Ren LQ. Antireflective surface inspired from biology: a review. Biosurf Biotribol. 2016;2:137–50.View ArticleGoogle Scholar
  5. Palasantzas G, De Hosson JTM, Michielsen KFL, Stavenga DG: Optical properties and wettability of nanostructured biomaterials: moth eyes, lotus leaves, and insect wings. In: Nalwa HS, editor. Handbook of nanostructured biomaterials and their applications in nanobiotechnology. Volume 1. London: American Scientific Publishers; 2005. p. 273–301.Google Scholar
  6. Deinega A, Valuev I, Potapkin B, Lozovik Y. Minimizing light reflection from dielectric textured surfaces. J Opt Soc Am Opt Image Sci Vis. 2011;28:770–7.View ArticleGoogle Scholar
  7. Dewan R, Fischer S, Meyer-Rochow VB, Ozdemir Y, Hamraz S, Knipp D. Studying nanostructured nipple arrays of moth eye facets helps to design better thin film solar cells. Bioinspir Biomim. 2012;7:016003.View ArticleGoogle Scholar
  8. Blagodatski A, Sergeev A, Kryuchkov M, Lopatina Y, Katanaev VL. Diverse set of turing nanopatterns coat corneae across insect lineages. Proc Natl Acad Sci USA. 2015;112:10750–5.View ArticleGoogle Scholar
  9. Blagodatski A, Kryuchkov M, Sergeev A, Klimov AA, Shcherbakov MR, Enin GA, Katanaev VL. Under- and over-water halves of Gyrinidae beetle eyes harbor different corneal nanocoatings providing adaptation to the water and air environments. Sci Rep. 2014;4:6004.View ArticleGoogle Scholar
  10. Kryuchkov M, Lehmann J, Schaab J, Fiebig M, Katanaev VL. Antireflective nanocoatings for UV-sensation: the case of predatory owlfly insects. J Nanobiotechnol. 2017;15:52.View ArticleGoogle Scholar
  11. Oskooi A, Favuzzi PA, Tanaka Y, Shigeta H, Kawakami Y, Noda S. Partially disordered photonic-crystal thin films for enhanced and robust photovoltaics. App Phys Lett. 2012;100:18110.View ArticleGoogle Scholar
  12. Pratesi F, Burresi M, Riboli F, Vynck K, Wiersma DS. Disordered photonic structures for light harvesting in solar cells. Opt Express. 2013;21:A460–8.View ArticleGoogle Scholar
  13. Xin Y, Jin H, Feng G, Hongjie L, Laixi S, Lianghong Y, Xiaodong J, Weidong W, Wanguo Z. High power laser antireflection subwavelength grating on fused silica by colloidal lithography. J Phys D Appl Phys. 2016;49:265104.View ArticleGoogle Scholar
  14. Daglar B, Khudiyev T, Demirel GB, Buyukserin F, Bayindir M. Soft biomimetic tapered nanostructures for large-area antireflective surfaces and SERS sensing. J Mater Chem C. 2013;1:7842–8.View ArticleGoogle Scholar
  15. Fraser MJ Jr. Insect transgenesis: current applications and future prospects. Annu Rev Entomol. 2012;57:267–89.View ArticleGoogle Scholar
  16. Kryuchkov M, Katanaev VL, Enin GA, Sergeev A, Timchenko AA, Serdyuk IN. Analysis of micro- and nano-structures of the corneal surface of Drosophila and its mutants by atomic force microscopy and optical diffraction. PLoS ONE. 2011;6:e22237.View ArticleGoogle Scholar
  17. Sergeev A, Timchenko AA, Kryuchkov M, Blagodatski A, Enin GA, Katanaev VL. Origin of order in bionanostructures. Rsc Adv. 2015;5:63521–7.View ArticleGoogle Scholar
  18. Xia Q, Guo Y, Zhang Z, Li D, Xuan Z, Li Z, Dai F, Li Y, Cheng D, Li R, et al. Complete resequencing of 40 genomes reveals domestication events and genes in silkworm (Bombyx). Science. 2009;326:433–6.View ArticleGoogle Scholar
  19. Xia Q, Li S, Feng Q. Advances in silkworm studies accelerated by the genome sequencing of Bombyx mori. Annu Rev Entomol. 2014;59:513–36.View ArticleGoogle Scholar
  20. Banno Y, Shimada T, Kajiura Z, Sezutsu H. The silkworm-an attractive BioResource supplied by Japan. Exp Anim. 2010;59:139–46.View ArticleGoogle Scholar
  21. Martins ER, Li J, Liu Y, Depauw V, Chen Z, Zhou J, Krauss TF. Deterministic quasi-random nanostructures for photon control. Nature communications. 2013;4:2665.View ArticleGoogle Scholar
  22. van Lare MC, Polman A. Optimized scattering power spectral density of photovoltaic light-trapping patterns. ACS Photonics. 2015;2:822–31.View ArticleGoogle Scholar
  23. Yu YF, Zhu AY, Paniagua-Dominguez R, Fu YH, Luk’yanchuk B, Kuznetsov AI. High-transmission dielectric metasurface with 2 phase control at visible wavelengths. Laser Photonics Rev. 2015;9:412–8.View ArticleGoogle Scholar
  24. Aghaeipour M, Anttu N, Nylund G, Samuelson L, Lehmann S, Pistol M-E. Tunable absorption resonances in the ultraviolet for InP nanowire arrays. Opt Express. 2014;22:29204–12.View ArticleGoogle Scholar
  25. Ji S, Park J, Lim H. Improved antireflection properties of moth eye mimicking nanopillars on transparent glass: flat antireflection and color tuning. Nanoscale. 2012;4:4603–10.View ArticleGoogle Scholar
  26. Anderson MS, Gaimari SD. Raman-atomic force microscopy of the ommatidial surfaces of Dipteran compound eyes. J Struct Biol. 2003;142:364–8.View ArticleGoogle Scholar
  27. Nickerl J, Tsurkan M, Hensel R, Neinhuis C, Werner C. The multi-layered protective cuticle of Collembola: a chemical analysis. J R Soc Interface. 2014;11:20140619.View ArticleGoogle Scholar
  28. Willis JH. Structural cuticular proteins from arthropods: annotation, nomenclature, and sequence characteristics in the genomics era. Insect Biochem Mol Biol. 2010;40:189–204.View ArticleGoogle Scholar
  29. Guo Y, Shen YH, Sun W, Kishino H, Xiang ZH, Zhang Z. Nucleotide diversity and selection signature in the domesticated silkworm, Bombyx mori, and wild silkworm, Bombyx mandarina. J Insect Sci. 2011;11:155.Google Scholar
  30. Katanaev VL, Kryuchkov MV. The eye of Drosophila as a model system for studying intracellular signaling in ontogenesis and pathogenesis. Biochemistry (Mosc). 2011;76:1556–81.View ArticleGoogle Scholar
  31. Son J, Verma LK, Danner AJ, Bhatia CS, Yang H. Enhancement of optical transmission with random nanohole structures. Opt Express. 2011;19:A35–40.View ArticleGoogle Scholar
  32. Necas D, Klapetek P. Gwyddion: an open-source software for SPM data analysis. Cent Eur J Phys. 2012;10:181–8.Google Scholar


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