Method for nucleic acid sequencing
US-2018258481-A1 · Sep 13, 2018 · US
US10343350B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10343350-B2 |
| Application number | US-201715411780-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 20, 2017 |
| Priority date | Feb 8, 2010 |
| Publication date | Jul 9, 2019 |
| Grant date | Jul 9, 2019 |
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Techniques for forming a nanopore in a lipid bilayer are described herein. In one example, an agitation stimulus level such as an electrical agitation stimulus is applied to a lipid bilayer wherein the agitation stimulus level tends to facilitate the formation of nanopores in the lipid bilayer. In some embodiments, a change in an electrical property of the lipid bilayer resulting from the formation of the nanopore in the lipid bilayer is detected, and a nanopore has formed in the lipid bilayer is determined based on the detected change in the lipid bilayer electrical property.
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What is claimed is: 1. A system for forming a nanopore in a lipid bilayer including: a surface on which the lipid bilayer forms; a source that is coupled to the surface; a sensing circuit coupled to the source; and a processor; wherein the processor is programmed to: determine that the lipid bilayer is formed on the surface based on a first measurement from the sensing circuit; in response to the determination that the lipid bilayer is formed and after nanopore forming molecules are deposited on the lipid bilayer, control the source to apply an agitation stimulus level to the lipid bilayer for up to one second, causing a disruption in the lipid bilayer that tends to facilitate the formation of the nanopore in the lipid bilayer; and control the source to apply a checking stimulus level following the agitation stimulus level to the lipid bilayer and determine that the nanopore has been formed based on a second measurement received from the sensing circuit sensing in response to the checking stimulus level, wherein an absolute magnitude of the agitation stimulus level is at least two times greater than an absolute magnitude of the checking stimulus level. 2. The system of claim 1 , further comprising an additional source, and wherein the processor is programmed to: in response to the determination that the lipid bilayer is formed and after nanopore forming molecules are deposited on the lipid bilayer, control the additional source to apply an additional agitation stimulus to the lipid bilayer, causing a disruption in the lipid bilayer that tends to facilitate the formation of the nanopore in the lipid bilayer, wherein the additional agitation stimulus is selected from the group consisting of: a mechanical stimulus, a sound stimulus, a chemical light stimulus, and a thermal stimulus. 3. The system of claim 1 , wherein the agitation stimulus level comprises a voltage (V) level. 4. The system of claim 1 , wherein the agitation stimulus level tends to facilitate an insertion of an α-hemolysin nanopore in the lipid bilayer. 5. The system of claim 1 , wherein: the sensing circuit is configured to detect a change in an electrical property of the lipid bilayer resulting from the formation of the nanopore in the lipid bilayer; and wherein the processor is programmed to determine that the nanopore has formed in the lipid bilayer based on the detected change in the lipid bilayer electrical property. 6. The system of claim 5 , wherein detecting a change in the lipid bilayer electrical property comprises detecting a change in a resistance of the lipid bilayer. 7. The system of claim 5 , wherein determining that the nanopore has formed includes determining a number of nanopores formed based on a size of change in the lipid bilayer electrical property. 8. The system of claim 7 , the processor is further programmed to control the source to apply an erasing electrical stimulus to erase the lipid bilayer when it is determined that more than one nanopore is formed in the lipid bilayer. 9. The system of claim 7 , the processor is further programmed to control the source to apply another agitation stimulus level to a lipid bilayer wherein the another agitation stimulus level tends to facilitate the formation of the nanopore in the lipid bilayer when it is determined that no nanopore is formed in the lipid bilayer. 10. The system of claim 5 , wherein detecting a change in the electrical property of the lipid bilayer resulting from the formation of the nanopore in the lipid bilayer includes detecting a decrease in resistance of the lipid bilayer. 11. The system of claim 1 , wherein the surface comprises a substantially planar hydrophilic solid surface. 12. The system of claim 1 , wherein the surface comprises a substantially planar electrode surface. 13. The system of claim 1 , wherein the system is automated. 14. The system of claim 1 , wherein the nanopore is one of a plurality of nanopores in a nanopore array. 15. The system of claim 14 , wherein each of the plurality of nanopores is individually addressable. 16. The system of claim 14 , wherein each of the plurality of nanopores is individually controllable.
having step or means utilizing mechanical or thermal property, e.g. pressure, heat · CPC title
Methods for sequencing · CPC title
Lipid particle · CPC title
Investigating individual macromolecules, e.g. by translocation through nanopores (Coulter counters in general G01N15/12; fabrication methods for nanoscale apertures B81B1/00; sequencing of nucleic acids C12Q1/68) · CPC title
Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic · CPC title
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