AI Article Synopsis

  • The study introduces a new technique that combines dynamic force microscopy with single molecule recognition force spectroscopy to capture topography images and identify specific binding sites with nanometer precision.
  • The researchers used lysozyme on mica and characterized its functionality with enzyme immunoassays, using antibody-coated tips that oscillated magnetically during imaging.
  • By analyzing the distinct deflections of the cantilever oscillations, the method effectively separated topographic data from binding recognition data, allowing for simultaneous recording of both types of images with high accuracy.

Article Abstract

We present a method for simultaneously recording topography images and localizing specific binding sites with nm positional accuracy by combining dynamic force microscopy with single molecule recognition force spectroscopy. For this we used lysozyme adsorbed to mica, the functionality of which was characterized by enzyme immunoassays. The topography and recognition images were acquired using tips that were magnetically oscillated during scanning and contained antibodies directed against lysozyme. For cantilevers with low Q-factor (approximately 1 in liquid) driven at frequencies below resonance, the surface contact only affected the downward deflections (minima) of the oscillations, whereas binding of the antibody on the tip to lysozyme on the surface only affected the upwards deflections (maxima) of the oscillations. The recognition signals were therefore well separated from the topographic signals, both in space (Delta z approximately 5 nm) and time (approximately 0.1 ms). Topography and recognition images were simultaneously recorded using a specially designed electronic circuit with which the maxima (U(up)) and the minima (U(down)) of each sinusoidal cantilever deflection period were depicted. U(down) was used for driving the feedback loop to record the height (topography) image, and U(up) provided the data for the recognition image.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1304601PMC
http://dx.doi.org/10.1529/biophysj.104.043331DOI Listing

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