Massively parallel synthesis of biopolymeric arrays

Patent metadata

Field	Value
Publication number	US-9499578-B2
Application number	US-13319008-A
Country	US
Kind code	B2
Filing date	Jun 4, 2008
Priority date	Dec 29, 2005
Publication date	Nov 22, 2016
Grant date	Nov 22, 2016

Abstract

Methods for fabricating dense arrays of polymeric molecules in a highly multiplexed manner are provided using semiconductor-processing-derived lithographic methods. Advantageously, the methods are adaptable to the synthesis of a variety of polymeric compounds. For example, arrays of branched peptides and polymers joined by peptide bonds may be fabricated in a highly multiplexed manner.

First claim

The invention claimed is:

1. A method for making an array of biopolymers comprising, attaching to a substrate surface a first molecule capable of forming a peptide bond wherein the molecule contains a first functional group capable of attaching to the surface of the substrate, a second functional group capable of forming a peptide bond, and a photo-removable protecting group that prevents the formation of a peptide bond by the second functional group,
exposing a portion of the substrate surface to ultraviolet radiation in the presence of microwave energy, wherein the ultraviolet radiation exposure causes the removal of the protecting group,
coupling a second molecule capable of forming three peptide bonds, wherein the molecule contains a first functional group capable of forming a peptide bond with the first molecule, a second and third functional group capable of forming a peptide bond, and two different photo-removable protecting groups capable of preventing the formation of a peptide bond, to the first molecule capable of forming a peptide bond that has been deprotected.

2. The method according to claim 1 wherein attaching is accomplished through the formation of a peptide bond.

3. The method according to claim 1 wherein the substrate surface to which the first molecule capable of forming a peptide bond is attached is an amino-functionalized SiO 2 surface.

4. The method according to claim 1 or 3 wherein the substrate is comprised of silicon having a layer of SiO 2 on the surface.

5. The method of claim 1 wherein a feature size of the array is less than 100 μm 2 .

6. The method of claim 1 wherein the array contains 1,000 to 10,000 features.

7. The method according to claim 1 also including exposing a portion of the substrate surface to radiation wherein radiation exposure causes the removal of a first one of the two protecting groups that is photo-removable on the second molecule, and
coupling a third molecule capable of forming a peptide bond, wherein the third molecule contains a first functional group capable of forming a peptide bond with the second molecule, a second functional group capable of forming a peptide bond, and a protecting group that is photoremovable and capable of preventing the formation of a peptide bond, to the second molecule capable of forming two different peptide bonds that has been deprotected at one peptide-bond forming site.

8. The method according to claim 7 , additionally including exposing a portion of the substrate surface to radiation wherein radiation exposure causes the removal of a protecting group on the third molecule that is photo-removable, and coupling a fourth molecule capable of forming a peptide bond, wherein the fourth molecule contains a first functional group capable of forming a peptide bond with the third molecule, a second functional group capable of forming a peptide bond, and a protecting group capable of preventing the formation of a peptide bond by the second functional group, to the third molecule, and repeating the elements of exposing and coupling with additional molecules to form a branched peptide attached to the substrate surface having a length from about 4 peptide bonds to about 25 peptide bonds.

9. The method of claim 1 wherein a molecule capable of forming a peptide bond is a spacer molecule selected from the group consisting of aryl acetylenes, polyethyleneglycols, nascent polypeptides, diamines, diacids, peptides, and combinations thereof.

10. The method of claim 7 wherein exposing the surface to radiation comprises exposing the surface to ultraviolet radiation at a first wavelength that causes the removal of the first one of the two protecting groups on the second molecule and exposing the surface to microwave radiation.

11. The method of claim 7 additionally including exposing a portion of the substrate surface to radiation wherein radiation exposure causes the removal of the second one of the two protecting groups that is photo-removable on the second molecule, and
coupling a fourth molecule capable of forming a peptide bond, wherein the fourth molecule contains a first functional group capable of forming a peptide bond with the second molecule, a second functional group capable of forming a peptide bond, and a protecting group that is photoremovable and capable of preventing the formation of a peptide bond, to the second molecule capable of forming two different peptide bonds that has been deprotected at one peptide-bond forming site.

12. The method of claim 11 wherein exposing the surface to radiation comprises exposing the surface to ultraviolet radiation at a second wavelength that causes the removal of the second of the two protecting groups on the second molecule and exposing the surface to microwave radiation.

Assignees

• Rajasekaran John J
• Cabezas Edelmira
• Fidanza Jacqueline A
• Tiwari Gunjan
• Intel Corp

Inventors

• Rajasekaran John J
• Cabezas Edelmira
• Fidanza Jacqueline A
• Tiwari Gunjan

Classifications

• C07K1/047 Primary

  Simultaneous synthesis of different peptide species; Peptide libraries · CPC title