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Ligand-Responsive Artificial Protein–Protein Communication for Field-Deployable Cell-Free Biosensing

Angew Chem Int Ed Engl. 2025-01; 
Ke Wang , Siqian Liu , Shuqi Zhou , Aori Qileng , Dingyi Wang , Yingju Liu , Chunlai Chen , Chunyang Lei , Zhou Nie
Products/Services Used Details Operation
PCR Cloning and Subcloning and a T7 terminator, was synthesized by Genscript Co. Ltd. (Nanjing, China) and then cloned into pET28a expression vector. Get A Quote

摘要

Natural protein-protein communications, such as those between transcription factors (TFs) and RNA polymerases/ribosomes, underpin cell-free biosensing systems operating on the transcription/translation (TXTL) paradigm. However, their deployment in field analysis is hampered by the delayed response (hour-level) and the complex composition of in vitro TXTL systems. For this purpose, we present a de novo-designed ligand-responsive artificial protein-protein communication (LIRAC) by redefining the connection between TFs and non-interacting CRISPR/Cas enzymes. By rationally designing a chimeric DNA adaptor and precisely regulating its binding affinities to both proteins, LIRAC immediately transduces target-induced T... More

关键词

Biosensing; CRISPR/Cas; DNA Engineering; Protein–protein Communication; Synthetic Biology.