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<oembed><version>1.0</version><provider_name>Future News 24</provider_name><provider_url>https://futurenews24.com</provider_url><author_name>Future News 24</author_name><author_url>https://futurenews24.com/index.php/author/mridulpahuja20/</author_url><title>Clear silk hydrogels as a flexible platform for cell tradition and imaging - Future News 24</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="vhMCyUBduy"&gt;&lt;a href="https://futurenews24.com/index.php/2026/07/25/s43246-026-01299-3/"&gt;Clear silk hydrogels as a flexible platform for cell tradition and imaging&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://futurenews24.com/index.php/2026/07/25/s43246-026-01299-3/embed/#?secret=vhMCyUBduy" width="600" height="338" title="&#x201C;Clear silk hydrogels as a flexible platform for cell tradition and imaging&#x201D; &#x2014; Future News 24" data-secret="vhMCyUBduy" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script&gt;
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</html><thumbnail_url>https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs43246-026-01299-3/MediaObjects/43246_2026_1299_Figa_HTML.png</thumbnail_url><thumbnail_width>1024</thumbnail_width><thumbnail_height>1024</thumbnail_height><description>Recombinant spider silk proteins (spidroins) are emerging as a promising feedstock for biomaterial production due to their inherent ability to form hydrogels at 37&#x2009;&#xB0;C. However, their broader application as a robust cell culture platform has been hindered by slow gelation kinetics, CO2-induced turbidity, unknown long-term stability, and the use of Tris-HCl buffers that are suboptimal for most mammalian cells. In this study, we aimed to accelerate gelation kinetics of mini-spidroin-based hydrogels, reduce their turbidity, and improve gel stability under physiological conditions. Systematic evaluation of protein pre-treatments and buffer compositions identified parameters governing conformational behavior, gelation dynamics, and structural stability. Multimodal characterization, including turbidity measurements, circular dichroism spectroscopy, Fourier-transform infrared spectroscopy, mechanical assessment, transmission electron microscopy, Thioflavin T assays, and in vitro studies, enabled the formulation of a cytocompatible buffer system optimized for mini-spidroin hydrogels. The formulation improves transparency and accelerates gelation, while maintaining experimental simplicity, thereby advancing the utility of mini-spidroin hydrogels as cell culture platforms. This study accelerates gelation kinetics of mini-spidroin-based hydrogels. By identifying parameters that govern conformational behavior, gelation dynamics, and structural stability, a cytocompatible buffer system is optimized, improving optical transparency.</description></oembed>
