ArticleiScience2026
High-throughput screening of FRET-based proteins using a hyperspectral microcapillary array.
Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
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Abstract
Fluorescence resonance energy transfer (FRET) is a versatile technique used in biology, chemistry, and materials science that involves distance-dependent energy transfer between light-sensitive molecules. Current FRET screening methods are limited in their ability to manage ultra-high-throughput samples. Challenges include low dynamic range, spectral overlap, multiple fluorophores, and high background signals. A high-throughput FRET approach enables rapid, multiplexed screening of interactions, conformations, and dynamics with accurate, real-time measurements. We developed a hyperspectral, high-throughput microcapillary array (HyCAP) that is well-suited for sorting large clone libraries based on fluorescence assays. Our platform provides sensitive, high-resolution hyperspectral imaging with a throughput of approximately 10
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