Particle patterning chip
This invention provides devices comprising substrates with wells for the patterning of particles or cells. Such devices are loaded with a suspension of particles or cell, and the entrapped particles or cells are transferred to a second substrate, where patterning of individual particles or cells occurs. Methods of cellular analysis, cell growth studies, surface modification, optical display fabrication and curved surface patterning using devices of this invention are described.
1. A method of particle patterning comprising the steps of:
a. providing a particle patterning device comprising a first substrate, wherein said first substrate contains an array of microwells, and loading particles onto said microwells, wherein:
i. said wells are sized so as to accommodate a requisite number of said loaded particles;
ii. said wells are positioned on or as a part of said substrate; and
iii. said wells are spaced at defined increments of from about 50 μm to about 50 mm between each well in said device;
b. flipping said first substrate upside down onto a second substrate wherein said second substrate is at a specified distance from said device;
whereby said particles are thereby deposited from said wells on said second substrate and patterned according to said defined increments.
2. The method of claim 1 , wherein said particles are cells or beads.
3. The method of claim 1 , wherein said particles are cells and said device is held at atmospheric conditions which promote cell adherence to and proliferation on said second substrate.
4. The method of claim 1 , wherein said second substrate is a 96-well plate.
5. The method of claim 1 , wherein said particles comprise a compound, a molecule or a macromolecule attached thereto.
6. The method of claim 5 , wherein said compound, molecule or macromolecule is a drug, and antibody, a nucleic acid, a peptide, a protein, or a chemical or nucleic acid library.
7. A method of patterning cells comprising the steps of:
a. providing a particle patterning device comprising a first substrate, wherein said first substrate contains an array of microwells, and loading cells onto said microwells, wherein:
i. said wells are sized so as to accommodate a requisite number of said loaded cells;
ii. said wells are positioned on or as a part of said substrate; and
iii. said wells are spaced at defined increments of from about 50 μm to about 50 mm between each well in said device;
b. flipping said first substrate upside down onto a second substrate wherein said second substrate is at a specified distance from said device, whereby said cells are thereby deposited from said wells on said second substrate and patterned according to said defined increments; and
c. analyzing said patterned cells.
8. The method of claim 7 , wherein said analyzing is conducted subsequent to cells spreading, proliferation, or a combination thereof.
9. The method of claim 7 , wherein said cells are engineered to express at least one desired molecule.
10. The method of claim 7 , wherein said cells are contacted with a library of drug molecules prior to said loading of said cells.
11. The method of claim 10 , wherein said cells are analyzed to determine the efficacy of said drug molecules in said patterned cells.
12. The method of claim 7 , wherein said cells are stem or progenitor cells.
13. The method of claim 12 , wherein said cells are engineered to express at least one desired protein.
14. The method of claim 13 , wherein said cells are cultured under conditions promoting expression of said protein.
15. The method of claim 14 , wherein said conditions that promote tissue engineering as a function of said expression.
16. The method of claim 7 , wherein said wells comprise individual cells.
17. The method of claim 7 , wherein said device is held at atmospheric conditions which promote cell adherence to and proliferation on said second substrate.
18. The method of claim 7 , wherein said second substrate is a 96-well plate.
19. The method of claim 7 , wherein said cells are engineered to express a desired nucleic acid molecule.
20. The method of claim 19 , wherein said cells express a nucleic acid library.
21. The method of claim 20 , further comprising the step of assaying said cells.
22. The method of claim 7 , wherein said analyzing comprises tracking spatial and temporal changes at the single-cell level.
23. The method of claim 7 , wherein said analyzing comprises detection of cell signalling in the patterned cells.
24. The method of claim 1 , wherein said second substrate is a 384-well plate.
25. The method of claim 7 , wherein said second substrate is a 384-well plate.