DNA: A Programmable Force Sensor
- 18 July 2003
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 301 (5631), 367-370
- https://doi.org/10.1126/science.1084713
Abstract
Direct quantification of biomolecular interaction by single-molecule force spectroscopy has evolved into a powerful tool for materials and life sciences. We introduce an approach in which the unbinding forces required to break intermolecular bonds are measured in a differential format by comparison with a known reference bond (here, a short DNAduplex). In addition to a marked increase in sensitivity and force resolution, which enabled us to resolve single–base pair mismatches, this concept allows for highly specific parallel assays. This option was exploited to overcome cross-reactions of antibodies in a protein biochip application.Keywords
This publication has 42 references indexed in Scilit:
- Protein microarrays and proteomicsNature Genetics, 2002
- DNA hybridization to mismatched templates: A chip studyPhysical Review E, 2002
- Structure and mechanics of single biomolecules: experiment and simulationJournal of Physics: Condensed Matter, 2002
- A perspective on protein microarraysNature Biotechnology, 2002
- Force Spectroscopy of Molecular Systems—Single Molecule Spectroscopy of Polymers and BiomoleculesPublished by Wiley ,2000
- How Strong Is a Covalent Bond?Science, 1999
- Adhesion Forces Between Individual Ligand-Receptor PairsScience, 1994
- Reaction-rate theory: fifty years after KramersReviews of Modern Physics, 1990
- Multi-analyte immunoassayJournal of Pharmaceutical and Biomedical Analysis, 1989
- Co-operative non-enzymatic base recognition III. Kinetics of the helix—coil transition of the oligoribouridylic · oligoriboadenylic acid system and of oligoriboadenylic acid alone at acidic pHJournal of Molecular Biology, 1971