From the words on this page to the scenery outside, we as a species are extremely dependent on, and in many ways, inspired by the colors and patterns that we see around us. Coloration in nature can be categorized into three forms: pigmentary coloration, structural coloration, and bioluminescence (Figure 1) ^{[1][2][3][4][5][6][7][8]}[1,2,3,4,5,6,7,8]. Pigmentary coloration is typically angle-independent coloration, where natural pigments directly absorb or reflect specific wavelengths of light (Figure 1A) ^{[1][2][3][4][5][6][7][8]}[1,2,3,4,5,6,7,8]. Structural coloration is often angle-dependent and involves the interference (i.e., reflection, transmittance, or scattering) of light by biological micro- or nano-structures with contrasting refractive indices (Figure 1B) ^{[1][2][3][4][5][6][7][8]}[1,2,3,4,5,6,7,8]. In comparison, bioluminescence typically involves the exergonic reactions of oxygen with different substrates and enzymes that lead to the production of visible photons of light (Figure 1C) ^{[1][2][3][4][5][6][7][8]}[1,2,3,4,5,6,7,8]. The variety of colors that result from these three photonic mechanisms in nature serves numerous functions, including camouflage, mimicry, aposematism, signaling, photosynthesis, and self-protection ^{[1][2][3][4][5][6][7][8]}[1,2,3,4,5,6,7,8]. These natural utility of such structures have also inspired and led to the design and engineering of materials with dynamic color changing capabilities (e.g., for infrared camouflage), anti-counterfeiting technologies, and a variety of displays and sensors ^{[9][10][11][12]}[9,10,11,12]. Nevertheless, the fundamental understanding of the molecular mechanisms that enable the formation (i.e., self-assembly) and dynamic tunability of these natural structures has been limited, which in turn has hindered the applications and engineering of biomolecule-based optical technologies. AIn this review, I showcase a few examples of pigmentary and structural coloration found in nature will be highlighted herein nature and highlight cephalopods as model organisms for dynamic structural coloration. Next, I discuss the current state-of-the-art strategies for structural and optical characterization of proteins. Finally, I outline a few potential directions for the study and engineering of optically-active proteins. Overall, this review aims to bring together the collective fields of biophotonic materials and structural coloration to emphasize the need for collaboration and an interdisciplinary approach to shed light on the biochemistry behind these astounding molecules.

Pigmentary coloration allows animals and plants to maintain bright coloration, which is often used to distinguish between species. Such forms of coloration are widely found in many mammals, birds, butterflies, fish and other marine organisms, and plants ^{[13][14][15][16][17][18][19][20][21][22][23][24][25][26][27]}[13,14,15,16,17,18,19,20,21,22,23,24,25,26,27]. For example, mammalian skin and hair/fur typically contain melanin variants which give the animals their specific colorations ^[13][14][13,14]. Interestingly, pigments are also found in the eye, within retinal pigment epithelial (RPE) cells in humans, where melanin and lipofuscin serve to absorb light and thereby reduce light damage in the eye ^[15][16][15,16]. Similar to humans and other mammals, melanin is also a common pigment found in bird feathers and exposed structures (e.g., skin and legs) ^[17][18][17,18]. The colors of birds are particularly diverse because of their reliance on visual cues for communication ^[17][18][17,18]. Typically, birds produce both eumelanins (black, brown, and grey coloration) and pheomelanins (yellow and red coloration) via cells known as melanosomes, where coated vesicles are known to actively transport chemical precursors to induce the formation of different melanins ^[17][18][17,18]. In addition to melanins, birds are also known to utilize carotenoids (largely acquired via their diet), along with other pigments, including flavins and porphyrins ^[17][18][17,18]. On the other hand, butterflies, which also boast a wide variety of colors and patterns, have papiliochrome pigments (yellow coloration), the carotenoid lutein (blue–green coloration), and variants of these pigments depending on the species ^{[19][20][21][22]}[19,20,21,22]. Notably, butterflies also use photoreceptors in their eyes to distinguish colors, likely in order to identify food sources, for mating, and to identify the locations of their host plants [23]. In contrast, fish have a variety of chromatophores (cells with pigment-based structures), including melanophores (which contain melanin), xanthophores (which contain yellow carotinoid-based pigments), and erythrophores (which contain red carotenoid-based pigments) ^[24][25][24,25]. More broadly, marine organisms also utilize carotenoids for their coloration, along with tetrapyrroles, quinones, azulenes, and melanins [26]. Some of the pigments found in these organisms are derived from their diets (e.g., carotenoids and tetrapyrroles), are found in the ink released by the organisms (e.g., tetrapyrroles in the purple ink of sea hares and melanin in the ink of cephalopods), or are produced by the organisms themselves (e.g., carotenoids in the lower trophic levels and anthraquinones in marine fungi) [26]. In comparison, the roles and diversity of pigments in plants likely surpass those known for animals, and specifically, plant pigmentation has a long history that is closely tied to the extraction and utilization of plant pigments as dyes and paints ^[27][28][29][27,28,29]. As one example, plants’ ability to perform photosynthesis is also critically dependent on pigment molecules such as chlorophylls (green pigments) and carotenoids (yellow, orange, and red pigments) ^[27][28][29][27,28,29]. Pigments such as flavonoids, including anthocyanins (pale yellow, pink/red, blue, and black pigments), and betalains (yellow or red pigments) can be found in the epidermal cells of flower petals, and are vital as visual signals for pollination and seed scattering, and thus in the interactions between plants and animals ^[27][28][29][27,28,29]. Altogether, pigments and pigment-based coloration represent a vibrant chemical modality for generating coloration; however, they generally produce angle-independent coloration that cannot be completely turned on or off, unlike structural coloration.

Structural coloration is also found in a variety of organisms, but in comparison to pigmentary coloration, allows the organism to generate colors at very specific wavelengths depending on the geometry (sizes and order) of the structures formed. For example, guanine crystals are found in the iridocytes of giant clams (Tridacninae) and form hexagonal structures below the cuticles of Sapphirinid copepods (Figure 2), where the arrangement and geometries of the structures formed by the guanine crystals lead to very different spectra observed for the animals ^[30][31][30,31]. Other forms of structural colors in organisms include 1D photonic crystals, as observed in Japanese jewel beetles (Chrysochroa fulgidissima) and other buprestids, Cicindela scutellaris beetles, Papilio ulysses butterflies, and the Coeligena prunellei hummingbird (Figure 3A–C) ^[32][33][34][32,33,34]. These insects and birds have alternating layers of chitin/melanin, chitin/air, or air/melanin in a keratin matrix with different periodicities that result in either the metallic hues of the beetles or the blue–green colors observed in the butterflies and hummingbirds ^[32][33][34][32,33,34]. Other structures, such as the lamellar membrane morphology observed in the iridosomes of zebrafish and the Delabrea michieana fruit enable narrowband light reflectance or iridescence (Figure 3D,E) ^[35][36][35,36]. In general, the iridosomes reflect specific wavelengths of light with particulate structures formed from high-refractive-index materials arranged within ribbon-like structures that form a one dimensional photonic crystal-like architecture composed of alternating high and low refractive index areas in the cells ^[35][36][35,36]. Similar multilayer reflectors have also been observed in various other species of butterflies and fish ^{[17][18][19][20][21][22]}[17,18,19,20,21,22]. Althogetherugh these examples demonstrate the diversitybroad range of structures that enable and thus examples of structural coloration in nature, the colors themselves are typically static (i.e., unchanging or changing over relatively long time-scales) or are influenced by the viewing angle of the observer rather than controlled by the organism itself.