Screening of cell populations

• US 6,277,588 B1
• Filed: 06/04/1998
• Issued: 08/21/2001
• Est. Priority Date: 05/01/1998
• Status: Expired due to Fees

• Current Assignee: Ramot University Authority For Applied Research and Industrial Development Limited, Tel Aviv University
• Original Assignee: Tel Aviv University
• Inventors: Georgiou, George, Freeman, Amihay
• Primary Examiner(s): GITOMER, RALPH J
• Application Number:
  US09/090,531
• Time in Patent Office: 1,174 Days
• Field of Search: 435/29, 435/30, 435/34, 435/182, 435/252.3, 435/320.1
• US Class Current: 435/30
• CPC Class Codes: C12Q 1/24 Methods of sampling, or inoculating or spreading a sample; Methods of physically isolating an intact microorganisms
• CPC Class Codes: G01N 33/5094 for blood cell populations red blood cells G01N33/80

Abstract

A method for screening large cell populations for isolation of mutants that express a target activity. The products of the screening method are disclosed. Various activities, including enzymatic activities can be selected.

Claims

1. A method for identification and isolation of a mutagenized cell or a clonal population of cells having an assayable activity comprising the steps of:

(a) non-selectively adsorbing substantially an entire mixed cell population onto the surface of derivatized cross-linked polymeric beads under conditions where each bead has either a single immobilized cell adhering to the bead surface, or has no cell adhering thereto;

(b) adsorbing and immobilizing the beads on a supporting surface;

(c) removing excess growth medium from the beads;

(d) equilibrating the beads with a substrate solution wherein said substrate solution produces a signal when acted on by said assayable activity thereby providing evidence of said assayable activity;

(e) removing excess substrate solution and incubating the beads carrying the cells on the surface of said beads under conditions that will allow the remaining substrate to be acted upon by the assayable activity to directly or indirectly produce evidence of the assayable activity;

(f) localizing the beads producing evidence of the assayable activity, thereby identifying the cells expressing the assayable activity; and

(g) isolating the cells producing evidence of the assayable activity by micro-manipulation, thereby forming a clonal population of cells on each bead.

2. The method of claim 1 wherein the beads are polyacrylarnide derivatized beads.

3. The method of claim 2 further comprising the step of incubating said immobilizcd cells on said beads that have been immobilizcd on said supporting surface in a growth medium under conditions wherein said immobilized cells proliferate and proceeding to step (c).

4. The method of claim 3 wherein said evidence is visually detectable.

5. The method of claim 4 wherein the assayable activity is an enzymatic activity.

6. The method of claim 5 wherein the evidence of the assayable activity is a color change.

7. The method of claim 6 wherein the mixed cell population is the product of random mutagenesis.

8. The method of claim 7 wherein the polyacrylamide beads are equilibrated with cell-growth medium prior to adsorbing the cells.

9. The method of claim 7 wherein the cell population is bacterial cells.

10. The method of claim 9 wherein a plurality of said beads each have a single immobilized cell on a surface of said bead.

11. The method of claim 10 wherein the visually detected evidence on the beads carrying a single cell on the surface of said bead is performed in parallel on a plurality of beads.

12. The method of claim 9 wherein the assayable activity is detected directly.

13. The method of claim 9 wherein the assayable activity is detected indirectly.

14. The method of claim 7 wherein the cells are mammalian cells.

15. The method of claim 1 wherein said derivatized cross-linked polymeric beads are pre-equilibrated in a liquid medium prior to step (a).

16. The method of claim 1 wherein said conditions of non-selectively adsorbing substantially an entire mixed population onto said surface of said derivatized cross-linked polymeric beads are combining said beads and said mixed cell population at a bead to cell ratio of at least 2:

1.

17. The method of claim 16 wherein said bead to cell ratio is at least 4:

1.