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  1. Abstract

    Nanostructured noble metals such as gold exhibit unique size‐dependent plasmonic and optical properties which is an enabling factor for designing nanophotonic devices. However, for its deployment in high temperature applications such as solar thermal energy harvesting and optothermal conversion, it requires understanding of its temperature dependent optical properties. This paper investigates the in situ specular reflectance of nanoporous gold (NPG) thin films in the wavelength range between 400 and 1000 nm at temperatures ranging from 25 to 500 °C via a home‐built fiber‐based optical spectrometer. During heating, the NPG's ligaments coalesce from an initial size of 39 ± 12 nm to a final size of up to 299 ± 114 nm, and its ligament scales with temperature closely matching an Arrhenius dependence. The surface roughness of NPG is empirically correlated to ligament size and temperature to allow for the theoretical prediction of the relative specular reflectance using scattering coefficients and effective medium theory which closely matches the experimental results. These results represent a step forward in using in situ optical spectroscopic methods to monitor the ligament size evolution of NPG thin‐films and to understand its stability and optical properties for applications at elevated temperatures.

     
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  2. Abstract Motivation

    Single-molecule localization microscopy (SMLM) can play an important role in integrated structural biology approaches to identify, localize and determine the 3D structure of cellular structures. While many tools exist for the 3D analysis and visualization of crystal or cryo-EM structures little exists for 3D SMLM data, which can provide unique insights but are particularly challenging to analyze in three dimensions especially in a dense cellular context.

    Results

    We developed 3DClusterViSu, a method based on 3D Voronoi tessellations that allows local density estimation, segmentation and quantification of 3D SMLM data and visualization of protein clusters within a 3D tool. We show its robust performance on microtubules and histone proteins H2B and CENP-A with distinct spatial distributions. 3DClusterViSu will favor multi-scale and multi-resolution synergies to allow integrating molecular and cellular levels in the analysis of macromolecular complexes.

    Availability and impementation

    3DClusterViSu is available under http://cbi-dev.igbmc.fr/cbi/voronoi3D.

    Supplementary information

    Supplementary figures are available at Bioinformatics online.

     
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