Published in

Cold Spring Harbor Protocols, 1(2012), p. pdb.prot067496-pdb.prot067496

DOI: 10.1101/pdb.prot067496



Export citation

Search in Google Scholar

Magnetic Trap Construction

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

Full text: Download

Green circle
Preprint: archiving allowed
Red circle
Postprint: archiving forbidden
Orange circle
Published version: archiving restricted
Data provided by SHERPA/RoMEO


In recent years, techniques have been developed to study and manipulate single molecules of DNA and other biopolymers. In one such technique, the magnetic trap, a single DNA molecule is bound at one end to a glass surface and at the other to a magnetic microbead. Small magnets, whose position and rotation can be controlled, pull on and rotate the microbead. This provides a simple method to stretch and twist the molecule. The system allows one to apply and measure forces ranging from 10(-3) to >100 picoNewtons (pN). In contrast to other techniques, the force measurement is absolute and does not require calibration of the sensor. This protocol describes a procedure for building and using a magnetic trap. It gives a method for constructing a microchamber suitable for magnetic tweezers studies, including antibody coating and passivation. It also describes a series of simple steps to achieve end-labeling of DNA anchoring fragments. One anchoring fragment is biotin-labeled and the other is labeled with digoxigenin. The anchoring fragments are then digested and ligated to a central DNA region containing the sequence of interest. The biotinylated DNA is adsorbed onto streptavidin-coated magnetic beads, and the DNA-bead mixture attaches specifically to the antidigoxigenin-coated surface of the microchamber.