Cohen Lab Research

Manipulating single molecules in solution  (with W. E. Moerner, Stanford)

The Anti-Brownian ELectrokinetic trap (ABEL trap) is a new device for trapping and manipulating single molecules in solution. It couples fluorescence microscopy to real-time electrokinetic feedback to control the motion of individual molecules in solution at room temperature.  A CCD camera connected to a computer tracks the Brownian motion of a single molecule.  The computer applies to the solution a time-varying feedback voltage so that the electrophoretic and electroosmotic drifts combine to cancel the Brownian motion.  The ABEL trap has been used to trap and study fluorescent quantum dots, molecules of DNA, fluorescently labeled lipid vesicles, single virus particles, and single molecules of large proteins.

This is a picture of a single 200 nm diameter fluorescent polystyrene nanosphere in the ABEL trap.

By analyzing the statistics of the feedback voltages it is possible to learn about the transport coefficients (diffusion coefficient and electrokinetic mobility) of a particle in the trap. After watching a particle in the trap, we can "undo" the effect of the feedback to reconstruct a pseudo-free trajectory statistically similar to the one it would have followed had it not been trapped.

The picture on the left shows the actual trajectories of 13 particles of Tobacco Mosaic Virus (TMV) held in the trap (lower right), and the statistically reconstructed pseudo-free trajectories for each of those particles.

 

Documentation:

Supporting info and press:

Movies:

  • Movie (680 k) of a single particle of Tobacco Mosaic Virus being manipulated in the ABEL trap. The virus particle is 15 nm wide and 300 nm long and is covalently labeled with Cy3. Note that midway through the movie the trapped particle interchanges with a different particle.
  • Movie (3.1 M) of a single fluorescent CdSe quantum dot held in the ABEL trap.
  • Movie (845 k) of a single molecule of the chaperonin GroEL held in the ABEL trap. The molecule starts with ~6 fluorescent molecules of Cy3, which photobleach one by one until the molecule becomes to dim to track and is lost from the trap. This experiment was performed in a solution of 50% glycerol to slow down the diffusion of the GroEL enough for the tracking and feedback to keep up with its motion.
  • Movie (8.5 M) of single molecules of double-stranded l-DNA being manipulated in the ABEL trap. The red "+" indicates the target position which is being controlled by the computer mouse.
  • Movie (4.0 M) of some particles in the trap subject to an arbitrary waveform (make sure sound is on
©2007 Adam E. Cohen