Method and system for automating sample preparation for microfluidic cryo TEM

• US 9,312,095 B2
• Filed: 03/24/2011
• Issued: 04/12/2016
• Est. Priority Date: 03/24/2010
• Status: Active Grant

• Current Assignee: Rhode Island Board of education (STATE OF RHODE ISLAND)
• Original Assignee: Brown University, Rhode Island Board of education (STATE OF RHODE ISLAND)
• Inventors: Tripathi, Anubhav, Lee, Jinkee, Bose, Arjit
• Primary Examiner(s): Jarrett, Ryan
• Application Number:
  US13/070,902
• Publication Number:
  US 20110238225A1
• Time in Patent Office: 1,846 Days
• Field of Search: 700/283
• US Class Current: 1/1
• CPC Class Codes: H01J 2237/2001 Maintaining constant desired temperature
• CPC Class Codes: H01J 2237/208 Elements or methods for movement independent of sample stage for influencing or moving or contacting or transferring the sample or parts thereof, e.g. prober needles or transfer needles in FIB/SEM systems
• CPC Class Codes: H01J 37/20 Means for supporting or positioning the object or the material; Means for adjusting diaphragms or lenses associated with the support

Abstract

A method and system is provided for automatically preparing transmission electron microscopy (TEM) samples for examination by depositing extremely small samples onto a grid without need for a blotting step. A sample liquid droplet is formed at the end of a capillary, wherein a portion of the liquid is transferred to the TEM sample grid by contact. The excess volume in the liquid droplet is then retracted by an adjacent capillary. After a predetermined time interval, the retraction capillary is moved toward the drop of the sample to remove the excess volume. As compared to a conventional machine, where the blotting procedure can deform the structure of the molecule of interest, the present invention utilizes a very low shear rate for removal of the excess sample fluid.

Claims

1. A method of preparing a cryogenic transmission electron microscopy sample grid, comprising:

providing a sample carrier grid having nanoscale sample openings;

forming a fluid droplet at the end of a first capillary;

bringing said droplet into contact with a top surface of said carrier grid thereby depositing said droplet onto said top surface; and

bringing a second capillary onto contact with said droplet to withdraw a portion of the fluid from said droplet to form a microfluidic sample on said top surface,

wherein said steps of forming a fluid droplet, bringing the droplet into contact with a top surface and bringing a second capillary into contact with the droplet are controlled using a computer.

2. The method of claim 1, further comprising:

after withdrawing a portion of said fluid, freezing said carrier grid with said microfluidic sample thereon.

3. The method of claim 1, wherein the computer controls an automated XYZ positioning system that positions the first capillary and controls a contact time between the fluid droplet and the top surface.

4. The method of claim 1, wherein the top surface of said carrier grid is hydrophilic.

5. A system for preparing a cryogenic transmission electron microscopy sample grid, comprising:

an automatic controller;

a first capillary for depositing fluid samples onto a sample carrier grid having nanoscale sample openings;

a second capillary for withdrawing a portion of said fluid samples; and

an automated XYZ positioning controller in communication with said automatic controller, said XYZ positioning controller controlling the position of said first and second capillaries,

wherein said automatic controller controls said first and second capillaries by,

forming a fluid droplet at the end of said first capillary;

bringing said droplet into contact with a top surface of a carrier grid thereby depositing said droplet onto said top surface; and

bringing said second capillary onto contact with said droplet to withdraw a portion of the fluid from said droplet to form a microfluidic sample on said top surface.

6. The system of claim 5, further comprising:

said automatic controller controlling freezing said carrier grid with said microfluidic sample thereon.

7. The system of claim 5, wherein said automatic controller controls said automated XYZ positioning controller to position the first capillary and control a contact time between the fluid droplet and the top surface.

8. The system of claim 5, wherein the top surface of said carrier grid is hydrophilic.