Chip based biosensor for functional analysis of single ion channels

@inproceedings{Vogel2000ChipBB,
  title={Chip based biosensor for functional analysis of single ion channels},
  author={Horst Vogel},
  year={2000}
}
  • H. Vogel
  • Published 1 September 2000
  • Biology
The functional anal. of single ion channel proteins presents a serious bottleneck in the process of finding new pharmacol. active compds. Currently available single channel recording methods are not suited for automation and miniaturization. However, new techniques such as combinatorial chem. and combinatorial genetics, which produce large amts. of potential drugs and mutant proteins, demand efficient and reliable screening as well as low sample consumption. Here we present a novel, silicon… 

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References

SHOWING 1-10 OF 31 REFERENCES

A biosensor that uses ion-channel switches

A biosensing technique in which the conductance of a population of molecular ion channels is switched by the recognition event, which mimics biological sensory functions and can be used with most types of receptor, including antibodies and nucleotides.

Stochastic sensing of organic analytes by a pore-forming protein containing a molecular adapter

It is shown that stochastic sensing of organic molecules can be procured from α-haemolysin by equipping the channel with an internal, non-covalently bound molecular ‘adapter’ which mediates channel blocking by the analyte.

Rapid nanopore discrimination between single polynucleotide molecules.

Because nanopores can rapidly discriminate and characterize unlabeled DNA molecules at low copy number, refinements of the experimental approach demonstrated here could eventually provide a low-cost high-throughput method of analyzing DNA polynucleotides.

Counting polymers moving through a single ion channel

This work shows that natural channel-forming peptides incorporated into a bilayer lipid membrane can be used to detect the passage of single molecules with gyration radii as small as 5–15 Å, and infer both the average number and the diffusion coefficients of poly(ethylene glycol) molecules in the pore.

Sorting single molecules: application to diagnostics and evolutionary biotechnology.

  • M. EigenR. Rigler
  • Biology, Physics
    Proceedings of the National Academy of Sciences of the United States of America
  • 1994
The method expands the horizon in molecular diagnostics by making it possible to monitor concentrations down to (less than) 10(-15) M without any need for amplification.

Supported Membranes: Scientific and Practical Applications

Supporting lipid-protein bilayers form versatile models of low-dimensionality complex fluids, which can be used to study interfacial forces and wetting phenomena, and enable the design of phantom cells to explore the interplay of lock-and-key forces and universal forces for cell adhesion.

Giant liposomes: a model system in which to obtain patch-clamp recordings of ionic channels.

It appears that the giant liposome technique offers a distinct advantage over other reconstitution procedures in that it provides a unique opportunity to undertake simultaneous biochemical, morphological, and electrophysiological studies of the incorporated ionic channel proteins.

Single binding versus single channel recordings: a new approach to study ionotropic receptors.

This work has simulated single ligand-binding events for the nicotinic acetylcholine receptor in order to provide comparisons with single channel events under pulsed agonist conditions.

Characterization of individual polynucleotide molecules using a membrane channel.

It is shown that an electric field can drive single-stranded RNA and DNA molecules through a 2.6-nm diameter ion channel in a lipid bilayer membrane, which could in principle provide direct, high-speed detection of the sequence of bases in single molecules of DNA or RNA.