Unknown

Dataset Information

0

Single-Molecule Assay for Proteolytic Susceptibility: Force-Induced Collagen Destabilization.


ABSTRACT: Force plays a key role in regulating dynamics of biomolecular structure and interactions, yet techniques are lacking to manipulate and continuously read out this response with high throughput. We present an enzymatic assay for force-dependent accessibility of structure that makes use of a wireless mini-radio centrifuge force microscope to provide a real-time readout of kinetics. The microscope is designed for ease of use, fits in a standard centrifuge bucket, and offers high-throughput, video-rate readout of individual proteolytic cleavage events. Proteolysis measurements on thousands of tethered collagen molecules show a load-enhanced trypsin sensitivity, indicating destabilization of the triple helix.

SUBMITTER: Kirkness MWH 

PROVIDER: S-EPMC5985029 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Single-Molecule Assay for Proteolytic Susceptibility: Force-Induced Collagen Destabilization.

Kirkness Michael W H MWH   Forde Nancy R NR  

Biophysical journal 20180201 3


Force plays a key role in regulating dynamics of biomolecular structure and interactions, yet techniques are lacking to manipulate and continuously read out this response with high throughput. We present an enzymatic assay for force-dependent accessibility of structure that makes use of a wireless mini-radio centrifuge force microscope to provide a real-time readout of kinetics. The microscope is designed for ease of use, fits in a standard centrifuge bucket, and offers high-throughput, video-ra  ...[more]

Similar Datasets

| S-EPMC2000387 | biostudies-literature
| S-EPMC3389265 | biostudies-literature
| S-EPMC4491811 | biostudies-other
| S-EPMC3594227 | biostudies-literature
| S-EPMC3088603 | biostudies-literature
| S-EPMC4676941 | biostudies-literature
| S-EPMC2553119 | biostudies-literature
| S-EPMC3397402 | biostudies-literature
| S-EPMC3113552 | biostudies-literature
| S-EPMC4800429 | biostudies-literature