Time-delay integration imaging of biological specimen

• US 20030048933A1
• Filed: 08/06/2002
• Published: 03/13/2003
• Est. Priority Date: 08/08/2001
• Status: Abandoned Application

• Current Assignee: Applied Precision Incorporated (General Electric Company)
• Original Assignee: Applied Precision Incorporated (General Electric Company)
• Inventors: Victor, Joseph J., Brown, Carl S.
• Application Number:
  US10/215,265
• Publication Number:
  US 20030048933A1
• Time in Patent Office: Days
• US Class Current: 382/128
• CPC Class Codes: B01J 2219/00274 Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
• CPC Class Codes: C07H 21/00 Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
• CPC Class Codes: G01N 2021/6441 with two or more labels
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/6452 Individual samples arranged in a regular 2D-array, e.g. multiwell plates
• CPC Class Codes: G01N 21/6456 Spatial resolved fluorescence measurements; Imaging

Abstract

A biological sample is scanned with Time-Delay Integration (TDI) by a CCD camera having columns and rows. When the light from a location of the sample falls onto a picture element (pixel) on the camera, the photons of the light are converted to electrons. The electrons within that pixel are shifted down one row to the pixel directly beneath it. The shifts occur in the columnar direction of the camera while the sample is moved synchronously with the electrons. The electrons shifted off the bottom row of the camera are measured and converted into a digital value for that picture element in the sample image.

Claims

1. A method for imaging biological specimens using an imaging chip having rows and columns, the method comprising:

capturing a pixel image of an object on the specimens;

shifting the pixel image in the columnar direction of the imaging chip;

moving the object in synchronous motion with the pixel image; and

reading out voltage values from the bottom row of the imaging chip until a plurality of the specimens are imaged.

2. The method of claim 1, wherein voltage values are read out from the bottom row of the imaging chip until all of the specimens are imaged.

3. The method of claim 1, wherein the biological specimens are immobilized on a microarray.

4. The method of claim 1, wherein the biological specimen comprises a nucleic acid or a polypeptide.

5. The method of claim 1 further comprising

digitizing the voltage values to produce a digital image strip.

6. The method of claim 5 further comprising

imaging other strips by changing an imaged area on the specimens;

and

joining together all the strips to form a final image.

7. The method of claim 5 wherein the digital image strip is a final image captured by a single wide optical detector.

8. The method of claim 1 further comprising adjusting exposure time of the image pixel by adjusting read out speed of the imaging chip.

9. The method of claim 1 further comprising adjusting exposure time of the image pixel by adjusting scan rate of the imaging chip.

10. The method of claim 1 wherein the object is moved at a constant speed.

11. The method of claim 1 wherein the object is held for exposure and is moved, one row at a time, down the imaging chip at the end of the exposure.

12. The method of claim 1 further comprising

measuring calibration data;

determining positional and rotational errors from the calibration data; and

modifying the position of an image area based on the errors.

13. The method of claim 1 further comprising

labeling the specimens with multiple indicators that respond to light of different wavelengths;

choosing a filter pair for a selected wavelength;

imaging the specimens with a single monochromatic detector through the filters to produce a component scan;

repeating the component scans for each of the wavelengths; and

combining the component scans to produce a multi-spectral image.

14. The method of claim 13 further comprising

measuring actual velocities and positions of the specimens for each of the component scans.

15. The method of claim 1 further comprising:

labeling the specimens with multiple indicators that respond to light of different wavelengths; and

simultaneously scanning the specimens with multiple monochromatic detectors.

16. The method of claim 1 further comprising:

labeling the specimens with multiple indicators that respond to light of different wavelengths; and

simultaneously scanning the specimens with a single monochromatic detector masked with a color mask.

17. A method for imaging a sample using an imaging device, the method comprising:

moving the position of an image area on the sample along one dimension of the device;

imaging a spot on the image area continuously until the imaged spot is moved out of the detection range of the device; and

adjusting the speed of the movement for adequate exposure time.

18. The method of claim 17 wherein the sample comprises a fluorescently labeled biological sample.

19. The method of claim 17 wherein the sample comprises a microarray.

20. The method of claim 17, wherein the sample comprises a plurality of nucleic acids or polypeptides immobilized to a surface.

21. The method of claim 17 wherein the imaging device is a CCD camera with columns and rows.

22. The method of claim 21 wherein the image area is moved along the columnar dimension of the CCD camera.

23. The method of claim 21 wherein the spot is held for exposure and is moved, one row at a time, down the CCD camera at the end of the exposure.

24. The method of claim 17 further comprising adjusting the exposure time of the image area by adjusting read out speed of the imaging device.

25. The method of claim 17 further comprising adjusting the exposure time of the image area by adjusting scan rate of the imaging device.

26. The method of claim 17 further comprising

measuring calibration data;

determining positional and rotational errors from the calibration data; and

modifying the position of the image area based on the errors.

27. The method of claim 17 further comprising

labeling the sample with multiple indicators that respond to light of different wavelengths;

choosing a filter pair for a selected wavelength;

imaging the sample with a single monochromatic detector through the filters to produce a component scan;

repeating the component scans for each of the wavelengths; and

combining the component scans to produce a multi-spectral image.

28. The method of claim 17 further comprising

measuring actual velocities and positions of the sample for each of the component scans.

29. The method of claim 17 further comprising:

labeling the sample with multiple indicators that respond to light of different wavelengths; and

simultaneously scanning the sample with multiple monochromatic detectors.

30. The method of claim 17 further comprising:

labeling the sample with multiple indicators that respond to light of different wavelengths; and

simultaneously scanning the sample with a single monochromatic detector masked with a color mask.