Micro-screening apparatus, process, and products

1. A method for screening a library of cells having a plurality of genotypes for a cell having a phenotype of interest for producing a molecule of interest, the method comprising

(a) loading a microcavity array with the library of cells;

(b) incubating the array under conditions that allow for production of the molecule of interest;

(c) imaging the array to identify a cavity comprising cells having the phenotype of interest; and

(d) extracting the contents of the cavity comprising cells having the phenotype of interest by directing electromagnetic radiation from a pulsed diode laser that delivers electromagnetic radiation in 2-20 pulses having pulse length of 1-10milliseconds with a pulse separation of 10 to 100 millisecond at a radiation absorbing material associated with the cavity.

2. The method of claim 1 , wherein the directing of electromagnetic radiation comprising applying the electromagnetic radiation to the radiation absorbing material to avoid heating a sample liquid in the cavity that is not in contact with the material.

3. The method of claim 1 , wherein the cells are expanded in the array.

4. The method of claim 1 , wherein the cells are selected from the group consisting of a mammalian cell, a yeast cell, and a bacterial cell.

5. The method of claim 4 , wherein the molecule of interest is displayed on the surface of a yeast cell or a bacterial cell.

6. The method of claim 4 , wherein the molecule of interest is secreted by a yeast cell or a bacterial cell.

7. The method of claim 1 , further comprising culturing the extracted contents of the cavities to produce a second-generation library of cells and repeating steps (a)-(d) with the second generation library.

8. The method of claim 1 , further comprising (1) extracting DNA from the cells comprising a gene for the phenotype of interest, (2) amplifying the DNA under conditions to introduce mutations in the gene; (3) creating a second generation library of cells comprising the amplified DNA, and (4) repeating steps (a)-(d) with the second generation library.

9. The method of claim 1 , wherein the phenotype of interest comprises a cell producing a binding agent.

10. The method of claim 9 , wherein the binding agent is a cell surface binding agent, an antibody, an antibody fragment, a ligand, a small molecule or a receptor.

11. The method of claim 1 , wherein the molecule of interest comprises a fluorescent protein that has at least one of an emission intensity of interest and an emission spectra of interest.

12. The method of claim 11 , wherein the scanning comprises identifying cavities emitting the at least one of the emission intensity of interest and the emission spectra of interest.

13. The method of claim 1 , wherein the phenotype of interest is a protein having an enzymatic activity, a protein having a lack of inhibition of enzyme activity, and a protein having activity in the presence of an inhibitor for the enzyme.

14. A method for engineering a property of interest in a fluorescent protein, wherein the property of interest comprises at least one of an emission spectra, an emission intensity, a stokes shift, and an absorption spectra, the method comprising creating a library of cells producing a mutant form of a fluorescent protein, and screening the library for cells producing the mutant form having the property of interest, wherein the screening method comprises:

(a) loading a microcavity array with the library of cells;

(b) incubating the array under conditions that allow for production of the mutant form;

(c) imaging the array to identify a cavity comprising cells producing the mutant form; and

(d) extracting the contents of the cavity comprising cells producing the mutant form by directing electromagnetic radiation from a pulsed diode laser that delivers electromagnetic radiation in 2-20 pulses having pulse length of 1-10milliseconds with a pulse separation of 10 to 100 millisecond at a radiation absorbing material associated with the cavity.

15. A method for measuring enzyme kinetics for a member of a protein enzyme library produced by a library of cells having a plurality of genotypes for producing mutant forms of a protein enzyme; the method comprising

(a) loading a microcavity array with the library of cells;

(b) incubating the array in the presence of a substrate for the protein enzyme under conditions that allow for production of the enzyme of interest;

(c) imaging the array at selected intervals;

(d) measuring difference in enzyme activity for one or more cavities of the array;

(e) extracting the contents of a cavity comprising cells having the phenotype of interest by directing electromagnetic radiation from a pulsed diode laser that delivers electromagnetic radiation in 2-20 pulses having pulse length of 1-10milliseconds with a pulse separation of 10 to 100 millisecond at a radiation absorbing material associated with the cavity.

16. The method of claim 15 , wherein the library of cells is a library of yeast cells or library of bacterial cells.

17. The method of claim 16 , wherein the protein enzymes are displayed on the surface of the cells.

18. The method of claim 16 , wherein the protein enzymes are secreted by the cells.

19. The method of claim 15 , further comprising adding an inhibitor for the enzyme.