IP Library Granted Patent US 8,808,516
Granted Patent B2
US 8,808,516 · App. 13/412,543 · Granted Aug 19, 2014

Devices and methods for long-term intracellular access

Inventors: Nicholas Alexander Melosh (Menlo Park, CA); Piyush Verma (Mountain View, CA); Benjamin David Almquist (Somerville, MA)
Assignee: The Board of Trustees of the Leland Stanford Junior University
G01N33/1826G01N33/18
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Quick Facts
Patent No.
US 8,808,516
App. No.
13/412,543
Granted
Aug 19, 2014
Kind
B2
Abstract

Nanoscale probes for forming stable, non-destructive seals with cell membranes. The probes, systems including these probes, and methods of fabricating and using the probes described herein may be used to sense from, stimulate, modify, or otherwise effect individual cells or groups of cells. In particular, described herein are nanoscale cellular probes that may be used to span the lipid membrane of a cell to provide stable and long lasting access to the internal cellular structures. Thus, the probes described herein may be used as part of a system, method or device that would benefit from stable, non-destructive access across a cell membrane. In some variations the nanoscale probe devices or systems described herein may be used as part of a drug screening procedure.

Claims (48)

1. A method of electrically recording from a cell, the method comprising:

contacting a cell membrane with a probe electrode comprising a base region and a post projecting from the base region, the post having a diameter of less than about 2 μm, a distal electrochemically active region, a proximal non-electrochemically active region, and a medial heterofunctional region between the distal electrochemically active region and the proximal non-electrochemically active region, wherein the medial heterofunctional region is more hydrophobic than either the distal electrochemically active region or the proximal non-electrochemically active region;

forming a seal with the cell membrane so that the electrochemically active region is in electrical communication with the cell and the medial heterofunctional region is held in the cell membrane; and

recording electrical activity with the probe electrode.

2. A method of establishing stable intracellular transmembrane access with a cell, the method comprising:

contacting the cell with a probe electrode having a base region and a post projecting from the base region, the post having a distal electrochemically active region and a proximal non-electrochemically active region, wherein the distal electrochemically active region is separated from the proximal non-electrochemically active region by a medial heterofunctional region forming a hydrophobic band around the post; and

fusing the hydrophobic band into the cell membrane.

3. A probe electrode for inserting through a cell membrane, the probe electrode comprising:

a base region including an electrical contact; and

a post projecting distally from the base region, the post having a diameter of less than about 2 μm, the post comprising:

a distal electrochemically active region in electrical communication with the electrical contact;

a proximal non-electrochemically active region that is electrically insulating and adjacent to the base region;

a medial heterofunctional region between the distal electrochemically active region and the proximal non-electrochemically active region, the medial heterofunctional region configured to form an annular hydrophobic region between the distal electrochemically active region and the proximal non-electrochemically active region.

4. A probe electrode for sealing with a cell membrane, the probe electrode comprising:

a base region including an electrical contact; and

a post projecting from the base region, the post having a diameter of less than about 2 μm, the post comprising:

a distal electrochemically active region in electrical communication with the electrical contact;

a proximal non-electrochemically active region adjacent to the base region; and

a medial heterofunctional region between the distal electrochemically active region and the proximal non-electrochemically active region, wherein the medial heterofunctional region is more hydrophobic than either the distal electrochemically active region or the proximal non-electrochemically active region.

5. The probe electrode of claim 4 , wherein the post comprises a diameter of less than 1000 nm.

6. The probe electrode of claim 4 , wherein the distal electrochemical region has a height of between about 20 nm and about 5 μm.

7. The probe electrode of claim 4 , wherein the distal electrochemical region is nanoporous.

8. The probe electrode of claim 4 , wherein the distal electrochemical region comprises one or more of: Pt; PtO; Ir; IrO; Ir 2 O 3 ; IrO 2 ; Ru; RuO 2 ; diamond; Au; graphite; Ni; V; Co; W; Mn; oxides of: Pt, PtO, Ir, IrO, Ir 2 O 3 , IrO 2 , Ru, RuO 2 , diamond, Au, graphite, Ni, V, Co, W, Mn; polyanaline; and poly(3,4 ethylene dioxythiophene).

9. The probe electrode of claim 4 , further comprising a conductive region in electrical contact with the distal electrochemically active region that extends through the proximal non-electrochemically active region to a connector on the base.

10. The probe electrode of claim 4 , wherein the non-electrochemically active region of the probe is formed of the same material as the base.

11. The probe electrode of claim 4 , wherein the proximal non-electrochemically active region comprises an electrically insulative material.

12. The probe electrode of claim 4 , wherein the post comprises a conical shape.

13. The probe of claim 4 wherein the medial heterofunctional region has a width of less than 200 nm.

14. The probe of claim 4 wherein the medial heterofunctional region has a width of between about 5 and about 10 nm.

15. The probe of claim 4 , further comprising a secondary medial region distal to the medial heterofunctional region configured to form a hydrophobic region.

16. The probe electrode of claim 4 , wherein the medial heterofunctional region forms a hydrophobic ring between the distal electrochemically active region and the proximal non-electrochemically active region.

17. The probe electrode of claim 4 , further comprising a distal functionalized region distal to the proximal non-electrochemically active region, wherein the distal functionalized region comprises an activity marker configured to indicate a cellular state or activity.

18. A probe electrode for inserting though a cell membrane, the probe electrode comprising:

a base region;

a post projecting from the base region, the post having a diameter of less than about 2 μm, the post comprising:

a distal electrochemically active region;

a proximal non-electrochemically active region adjacent to the base region comprising an electrically insulating material; and

a medial heterofunctional region between the distal electrochemically active region and the proximal non-electrochemically active region, wherein the medial heterofunctional region is configured to form a region that is more hydrophobic than either the distal electrochemically active region or the proximal non-electrochemically active region.

19. The probe electrode of claim 18 , wherein the distal electrochemical region has a height of between about 20 nm and about 5 μm.

20. The probe electrode of claim 18 , wherein the distal electrochemical region is nanoporous.

21. The probe electrode of claim 18 , further comprising a conducive region in electrical contact with the distal electrochemically active region that extends through the proximal non-electrochemically active region to a connector on the base region.

22. The probe electrode of claim 18 , wherein the non-electrochemically active region of the probe is formed of the same material as the base region.

23. The probe electrode of claim 18 , further comprising an electrical contact on the base region.

24. The probe electrode of claim 18 , wherein the medial heterofunctional region comprises an annular ring configured to bind to a molecule to form an annular hydrophobic region separating the distal electrochemically active region and the proximal non-electrochemically active region.

25. The probe of claim 18 wherein the medial heterofunctional region has a width of less than 200 nm.

26. The probe of claim 18 wherein the medial heterofunctional region has a width of between about 5 and about 10 nm.

27. The probe electrode of claim 18 , further comprising a distal functionalized region distal to the proximal non-electrochemically active region, wherein the distal functionalized region comprises an activity marker configured to indicate a cellular state or activity.

28. The probe electrode of claim 18 , further comprising a secondary medial region distal to the medial heterofunctional region configured to form a hydrophobic region.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2012
From: MELOSH, NICHOLAS ALEXANDER; VERMA, PIYUSH; ALMQUIST, BENJAMIN DAVID
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 028370/0725 →
CONFIRMATORY LICENSE Recorded May 10, 2012
From: STANFORD UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 028185/0540 →
Continuity (2)
Provisional Application 61449615 · Mar 4, 2011
Related Publication 20120222970A1 · Sep 6, 2012