ArticleJACS Au2026
Carbon Dots as Electrostatically Driven Base-Selective Chemical Compilers for Programmable Nucleic Acid Condensation.
Article in JACS Au, 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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13 authors.
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Abstract
Cells execute complex biological functions through programmed biomolecular condensation, yet a general and programmable strategy for nucleic acid condensation in vitro remains challenging. Here, we demonstrate that carbon dots (CDs) function as an electrostatic-driven versatile chemical compiler that translates nucleobase sequence into programmed condensate architectures and functions. We found that citric acid-ethylene diamine carbon dots (CA-EDA CDs) drive the condensation of both ssDNA and mRNA via multiple weak interactions. Crucially, the spatially heterogeneous electrostatic potential on the CD surface decodes the distinct electrostatic properties of nucleobases through Coulomb-dominated interactions, establishing a definitive binding hierarchy (G > C >
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