Methods for creating bilayers for use with nanopore sensors

Patent metadata

Field	Value
Publication number	US-9850534-B2
Application number	US-201314376836-A
Country	US
Kind code	B2
Filing date	Feb 15, 2013
Priority date	Feb 16, 2012
Publication date	Dec 26, 2017
Grant date	Dec 26, 2017

Abstract

The present disclosure provides biochips and methods for making biochips. A biochip can comprise a nanopore in a membrane (e.g., lipid bilayer) adjacent or in proximity to an electrode. Methods are described for forming the membrane and inserting the nanopore into the membrane. The biochips and methods can be used for nucleic acid (e.g., DNA) sequencing. The present disclosure also describes methods for detecting, sorting, and binning molecules (e.g., proteins) using biochips.

First claim

What is claimed is:

1. A method for forming a lipid bilayer for use in a nanopore sensor, comprising:
(a) directing an electrically conductive buffer solution in a flow channel comprising an electrode having a lipid material layer dried down thereon, wherein said lipid material layer comprises one or more lipids, and is capable of forming the lipid bilayer;
(i) directing a bubble through said flow channel and bringing said bubble in contact with said lipid material layer to smooth and/or thin said lipid material layer;
(ii) flowing a solution comprising a pore protein adjacent to said lipid material layer to deposit said pore protein in said lipid material layer, and thinning said lipid material layer with an additional bubble in said flow channel;

(b) bringing said buffer solution in contact with said lipid material layer to facilitate the formation of the lipid bilayer on top of said electrode, the pore protein solution and the buffer solution being separated by the additional bubble;
(c) measuring a current through said electrode to determine if at least a portion of said lipid material layer has formed said lipid bilayer adjacent to said electrode;
(d) based on the determination of (c), applying a stimulus to said electrode to induce said at least the portion of the material layer to form said lipid bilayer adjacent to said electrode; and
(e) applying a stimulus through said electrode to facilitate the insertion of the pore protein in said lipid bilayer.

2. The method of claim 1 , wherein, in (c), one or more voltages are applied to said electrode.

3. The method of claim 2 , wherein said voltage is selected to break or disrupt the bilayer over the electrode.

4. The method of claim 1 , wherein the stimulus is selected from the group consisting of a liquid flow over the surface of the electrode, a sequential flow of one or more different liquids over the surface of the electrode, a flow of one or more bubbles over the surface of the electrode, an electrical pulse, a sonication pulse, a pressure pulse, and a sound pulse.

5. The method of claim 1 , wherein the material layer comprising one or more porin proteins and one or more surfactants at a concentration less than the critical micelle concentration of the surfactant.

6. The method of claim 1 , wherein said flow channel comprises a plurality of electrodes, wherein said plurality of electrodes comprises said electrode.

7. The method of claim 6 , wherein the stimulus is applied simultaneously to said plurality of electrodes.

8. The method of claim 1 , wherein the material layer comprises at least two types of lipids.

9. The method of claim 1 , wherein the pore protein is selected from the group consisting of mycobacterium smegmatis porin A (MspA), alpha-hemolysin, and any protein having at least 70% homology to at least one of smegmatis porin A (MspA) or alpha-hemolysin.

10. The method of claim 1 , wherein said lipid bilayer and said pore protein together exhibit a resistance of about 1 GΩ or less.

11. The method of claim 1 , wherein said lipid bilayer without a pore protein exhibits a resistance greater than about 1 GΩ.

12. The method of claim 1 , wherein a pressure of said buffer solution is selected such that said material layer forms said lipid bilayer without said stimulus.

13. The method of claim 1 , further comprising, prior to (a), generating said material layer adjacent to said electrode.

14. The method of claim 13 , wherein said generating comprises:
directing a lipid solution comprising said one or more lipids through said flow channel; and
depositing said material layer on said electrode.

15. The method of claim 14 , wherein said lipid solution comprises an organic solvent.

16. The method of claim 15 , wherein said organic solvent comprises decane.

17. The method of claim 1 , wherein said buffer solution comprises an ionic solution.

18. The method of claim 17 , wherein the ionic solution comprises a chloride anion.

19. The method of claim 18 , wherein the ionic solution comprises sodium acetate.

20. The method of claim 1 , wherein said bubble is a vapor bubble.

21. The method of claim 1 , wherein said one or more lipids are selected from the group consisting of diphytanoylphosphatidylcholine (DPhPC), palmitoyl-oleoyl-phosphatidyl-choline (POPC), dioleoyl-phosphatidyl-methylester (DOPME), dipalmitoylphosphatidylcholine (DPPC), phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, phosphatidic acid, phosphatidylinositol, phosphatidylglycerol and sphingomyelin.

22. The method of claim 1 , wherein a surface of said electrode that is exposed to said flow channel is hydrophilic.

23. The method of claim 1 , wherein said electrode is disposed adjacent to one or more hydrophobic surfaces of the flow channel.

24. The method of claim 23 , wherein said one or more hydrophobic surfaces are silanized.

25. The method of claim 1 , wherein said flow channel is formed in a chip.

26. The method of claim 1 , wherein said electrode is formed in a surface of said flow channel.

27. The method of claim 1 , wherein said flow channel is sealed.

28. The method of claim 1 , wherein said one or more flow channels comprise a plurality of flow channels.

29. The method of claim 28 , wherein said plurality of flow channels are fluidically separated from one another with the aid of guide rails along said plurality of flow channels.

30. The method of claim 1 , wherein said electrode is an individually addressable electrode.

31. The method of claim 1 , wherein (c) further comprises determining if at least a portion of said material layer has formed a lipid bilayer over all or a portion of said electrode.

32. A method for forming a lipid bilayer for use in a nanopore sensor, comprising:
(a) providing a chip comprising a plurality of electrodes and lipid material layers adjacent to said plurality of electrodes, wherein each of said lipid material layers comprises a lipid capable of forming the lipid bilayer;
(i) directing a bubble through said flow channel and bringing said bubble in contact with said lipid material layer to smooth and/or thin said lipid material layer;
(ii) flowing a solution comprising a pore protein adjacent to said lipid material layer to deposit said pore protein in said lipid material layer, and thinning said lipid material layer with an additional bubble in said flow channel;

(b) contacting said lipid material layers with a buffer solution, wherein said buffer solution is electrically conductive, the pore protein solution and the buffer solution being separated by the additional bubble;
(c) applying a stimulus to at least a subset of said plurality of electrodes to induce said material layers to form lipid bilayers adjacent to the plurality of the electrodes; and
(d) repeating steps (b) and (c), as needed, until at least about 20% of said plurality of electrodes deactivate at a voltage pulse between about −100 millivolts (mV) and −1000 mV applied to said plurality of electrodes; and
(e) applying a stimulus through at least a subset of said plurality of electrodes to facilitate the insertion of said pore protein in each of said lipid bilayers.

33. The method of claim 32 , wherein said plurality of electrodes are each individually addressable.

34. The metho

Assignees

• Genia Tech Inc

Inventors

• Davis Randall
• Chen Roger

Classifications

• G01N33/48721

  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

• B01J2219/00734

  Lipids · CPC title

• C12Q1/6869 Primary

  Methods for sequencing · CPC title

• C12N2320/32

  Special delivery means, e.g. tissue-specific · CPC title

• C12Q2565/631

  being a biochannel or pore · CPC title