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Molecular force spectroscopy with a DNA origami-based nanoscopic force clamp.


ABSTRACT: Forces in biological systems are typically investigated at the single-molecule level with atomic force microscopy or optical and magnetic tweezers, but these techniques suffer from limited data throughput and their requirement for a physical connection to the macroscopic world. We introduce a self-assembled nanoscopic force clamp built from DNA that operates autonomously and allows massive parallelization. Single-stranded DNA sections of an origami structure acted as entropic springs and exerted controlled tension in the low piconewton range on a molecular system, whose conformational transitions were monitored by single-molecule Förster resonance energy transfer. We used the conformer switching of a Holliday junction as a benchmark and studied the TATA-binding protein-induced bending of a DNA duplex under tension. The observed suppression of bending above 10 piconewtons provides further evidence of mechanosensitivity in gene regulation.

SUBMITTER: Nickels PC 

PROVIDER: S-EPMC6546592 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature

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Molecular force spectroscopy with a DNA origami-based nanoscopic force clamp.

Nickels Philipp C PC   Wünsch Bettina B   Holzmeister Phil P   Bae Wooli W   Kneer Luisa M LM   Grohmann Dina D   Tinnefeld Philip P   Liedl Tim T  

Science (New York, N.Y.) 20161001 6310


Forces in biological systems are typically investigated at the single-molecule level with atomic force microscopy or optical and magnetic tweezers, but these techniques suffer from limited data throughput and their requirement for a physical connection to the macroscopic world. We introduce a self-assembled nanoscopic force clamp built from DNA that operates autonomously and allows massive parallelization. Single-stranded DNA sections of an origami structure acted as entropic springs and exerted  ...[more]

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