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Originally published as Biophys J. BioFAST on July 13, 2007.
doi:10.1529/biophysj.107.104737
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Biophysical Journal 93:3120-3131 (2007)
© 2007 The Biophysical Society

Nanopipette Delivery of Individual Molecules to Cellular Compartments for Single-Molecule Fluorescence Tracking

Andreas Bruckbauer *, Peter James {dagger}, Dejian Zhou *, Ji Won Yoon * {ddagger}, David Excell {ddagger}, Yuri Korchev §, Roy Jones {dagger} and David Klenerman *

* Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, United Kingdom; {dagger} Laboratory of Molecular Signalling, Babraham Institute, Cambridge CB2 4AT, United Kingdom; {ddagger} Department of Engineering, University of Cambridge, Cambridge CB2 1PZ, United Kingdom; and § Imperial College, Division of Medicine, London W12 0NN, United Kingdom

Correspondence: Address reprint requests to D. Klenerman, E-mail: dk10012{at}cam.ac.uk.

We have developed a new method, using a nanopipette, for controlled voltage-driven delivery of individual fluorescently labeled probe molecules to the plasma membrane which we used for single-molecule fluorescence tracking (SMT). The advantages of the method are 1), application of the probe to predefined regions on the membrane; 2), release of only one or a few molecules onto the cell surface; 3), when combined with total internal reflection fluorescence microscopy, very low background due to unbound molecules; and 4), the ability to first optimize the experiment and then repeat it on the same cell. We validated the method by performing an SMT study of the diffusion of individual membrane glycoproteins labeled with Atto 647-wheat germ agglutin in different surface domains of boar spermatozoa. We found little deviation from Brownian diffusion with a mean diffusion coefficient of 0.79 ± 0.04 µm2/s in the acrosomal region and 0.10 ± 0.02 µm2/s in the postacrosomal region; this difference probably reflects different membrane structures. We also showed that we can analyze diffusional properties of different subregions of the cell membrane and probe for the presence of diffusion barriers. It should be straightforward to extend this new method to other probes and cells, and it can be used as a new tool to investigate the cell membrane.




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J. W. Yoon, A. Bruckbauer, W. J. Fitzgerald, and D. Klenerman
Bayesian Inference for Improved Single Molecule Fluorescence Tracking
Biophys. J., June 15, 2008; 94(12): 4932 - 4947.
[Abstract] [Full Text] [PDF]




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