Revealing the Wonder of Natural Photonics by Nonlinear Optics

Nano-optics explores linear and nonlinear phenomena at the nanoscale to advance fundamental knowledge about materials and their interaction with light in the classical and quantum domains in order to develop new photonics-based technologies. In this perspective article, we review recent progress regarding the application of nonlinear optical methods to reveal the links between photonic structures and functions of natural photonic geometries. Furthermore, nonlinear optics offers a way to unveil and exploit the complexity of the natural world for developing new materials and technologies for the generation, detection, manipulation, and storage of light at the nanoscale, as well as sensing, metrology, and communication

Additive Photonic Colors in the Brazilian Diamond Weevil, Entimus imperialis

Structurally colored nano-architectures found in living organisms are complex optical materials, giving rise to multi-scale visual effects. In arthropods, these structures often consist of porous biopolymers and form natural photonic crystals. A signature of the structural origin of coloration in insects is iridescence, i.e., color changes with the viewing angle. In the scales located on the elytra of the Brazilian weevil Entimus imperialis (Curculionidae), three-dimensional photonic crystals are observed. On one hand, each of them interacts independently with light, producing a single color which is observed by optical microscopy and ranges from blue to orange. On the other hand, the color perceived by the naked eye is due to multi-length-scale light effects involving different orientations of a single photonic crystal. This disorder in crystal orientations alters the light propagation in such a way that the crystal iridescence is removed. Entimus imperialis is therefore a remarkable example of additive photonic colors produced by a complex multi-scale organic architecture. In order to study this specific natural photonic structure, electron microscopy is used. The structure turns out to be formed of a single type of photonic crystal with different orientations within each scale on the elytra. Our modeling approach takes into account the disorder in the photonic crystals and explains why the structure displays bright colors at the level of individual scales and a non-iridescent green color in the far-field.Structurally colored nano-architectures found in living organisms are complex optical materials, giving rise to multi-scale visual effects. In arthropods, these structures often consist of porous biopolymers and form natural photonic crystals. A signature of the structural origin of coloration in insects is iridescence, i.e., color changes with the viewing angle. In the scales located on the elytra of the Brazilian weevil Entimus imperialis (Curculionidae), three-dimensional photonic crystals are observed. On one hand, each of them interacts independently with light, producing a single color which is observed by optical microscopy and ranges from blue to orange. On the other hand, the color perceived by the naked eye is due to multi-length-scale light effects involving different orientations of a single photonic crystal. This disorder in crystal orientations alters the light propagation in such a way that the crystal iridescence is removed. Entimus imperialis is therefore a remarkable example of additive photonic colors produced by a complex multi-scale organic architecture. In order to study this specific natural photonic structure, electron microscopy is used. The structure turns out to be formed of a single type of photonic crystal with different orientations within each scale on the elytra. Our modeling approach takes into account the disorder in the photonic crystals and explains why the structure displays bright colors at the level of individual scales and a non-iridescent green color in the far-field

Light harvesting in photonic crystals revisited: why do slow photons at the blue edge enhance absorption?

Enhanced absorption in TiO2 inverse opals with blue-edge slow photons is explained by loose field confinement in thin TiO2 skeleton.</p

p53 requires the stress sensor USF1 to direct appropriate cell fate decision

Genomic instability is a major hallmark of cancer. To maintain genomic integrity, cells are equipped with dedicated sensors to monitor DNA repair or to force damaged cells into death programs. The tumor suppressor p53 is central in this process. Here, we report that the ubiquitous transcription factor Upstream Stimulatory factor 1 (USF1) coordinates p53 function in making proper cell fate decisions. USF1 stabilizes the p53 protein and promotes a transient cell cycle arrest, in the presence of DNA damage. Thus, cell proliferation is maintained inappropriately in Usf1 KO mice and in USF1-deficient melanoma cells challenged by genotoxic stress. We further demonstrate that the loss of USF1 compromises p53 stability by enhancing p53-MDM2 complex formation and MDM2-mediated degradation of p53. In USF1-deficient cells, the level of p53 can be restored by the re-expression of full-length USF1 protein similarly to what is observed using Nutlin-3, a specific inhibitor that prevents p53-MDM2 interaction. Consistent with a new function for USF1, a USF1 truncated protein lacking its DNA-binding and transactivation domains can also restore the induction and activity of p53. These findings establish that p53 function requires the ubiquitous stress sensor USF1 for appropriate cell fate decisions in response to DNA-damage. They underscore the new role of USF1 and give new clues of how p53 loss of function can occur in any cell type. Finally, these findings are of clinical relevance because they provide new therapeutic prospects in stabilizing and reactivating the p53 pathway

Merkel Cell Polyomavirus Small T Antigen mRNA Level Is Increased following In Vivo UV-Radiation

Merkel cell carcinoma (MCC) is a rare but aggressive skin cancer involving Merkel cells. Recently, a new human polyomavirus was implicated in MCC, being present in 80% of the samples analyzed. In virus-positive MCC, the Merkel cell polyomavirus (MCPyV) is clonally integrated into the patients DNA, and carries mutations in its large T antigen, leading to a truncated protein. In non-symptomatic tissue MCPyV can reside at very low levels. MCC is also associated with older age, immunosuppression and sun exposure. However, the link with solar exposure remains unknown, as the precise mechanism and steps involved between time of infection by MCPyV and the development of MCC. We thus investigated the potential impact of solar simulated radiation (SSR) on MCPyV transcriptional activity. We screened skin samples of 20 healthy patients enrolled in a photodermatological protocol based on in vivo-administered 2 and 4 J/cm2 SSR. Two patients were infected with two new variants of MCPyV, present in their episomal form and RT-QPCR analyses on SSR-irradiated skin samples showed a specific and unique dose-dependent increase of MCPyV small t antigen transcript. A luciferase based in vitro assay confirmed that small t promoter is indeed UV-inducible. These findings demonstrate that solar radiation has an impact on MCPyV mRNA levels that may explain the association between MCC and solar exposure