Miniature Laboratory for Detecting Sparse Biomolecules
- Monday, 01 August 2005
Specimens would be concentrated and sorted before detection.
The figure schematically depicts a miniature laboratory system that has been proposed for use in the field to detect sparsely distributed biomolecules. By emphasizing concentration and sorting of specimens prior to detection, the underlying system concept would make it possible to attain high detection sensitivities without the need to develop ever more sensitive biosensors.
The original purpose of the proposal is to aid the search for signs of life on a remote planet by enabling the detection of specimens as sparse as a few molecules or microbes in a large amount of soil, dust, rocks, water/ice, or other raw sample material. Some version of the system could prove useful on Earth for remote sensing of biological contamination, including agents of biological warfare.
Processing in this system would begin with dissolution of the raw sample material in a sample-separation vessel. The solution in the vessel would contain floating microscopic magnetic beads coated with substances that could engage in chemical reactions with various target functional groups that are parts of target molecules. The chemical reactions would cause the targeted molecules to be captured on the surfaces of the beads.
By use of a controlled magnetic field, the beads would be concentrated in a specified location in the vessel. Once the beads were thus concentrated, the rest of the solution would be discarded. This procedure would obviate the filtration steps and thereby also eliminate the filter-clogging difficulties of typical prior sample-concentration schemes. For ferrous dust/soil samples, the dissolution would be done first in a separate vessel before the solution is transferred to the microbead-containing vessel.
A small amount of a solvent solution would be used to elute the captured target molecules from the surfaces of the beads. The resulting solution would be made to flow through a series of capillary detection channels, which would be coated with probe molecules, each designed to capture a specific functional group. Once the flow had run its course, an instrument yet to be developed (perhaps an integrated optical spectrometer) would be used to detect and analyze molecules of interest that had accumulated in the channels. The outputs of the instrument would be used to construct a matrix of data from which the concentrations of the target molecules would be estimated.
This work was done by Ying Lin and Nan Yu of Caltech for NASA’s Jet Propulsion Laboratory. For further information, access the Technical Support Package (TSP ) free on-line at www.techbriefs.com/tsp under the Bio-Medical category. NPO-40281
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