Virion display array for profiling functions and interactions of human membrane proteins

Patent metadata

Field	Value
Publication number	US-10208290-B2
Application number	US-201414900314-A
Country	US
Kind code	B2
Filing date	Jun 20, 2014
Priority date	Jun 21, 2013
Publication date	Feb 19, 2019
Grant date	Feb 19, 2019

Abstract

Provided herein are recombinant virion arrays comprising human membrane bound proteins that retain their native conformations and/or interactions, recombinant HSV-1 virions, and methods of use including high-content, high-throughput assays for screening for ligands and/or drugs that bind human membrane bound proteins, diagnostic assays, proteomic assays, and biosensor assays. Also provided are recombinant HSV-1 virions comprising an envelope comprising a plurality of heterologous membrane bound proteins that retain their native conformations and/or interactions as well as recombinant HSV-1 bacterial artificial chromosome (BAC) clones encoding heterologous membrane polypeptides.

First claim

We claim:

1. An array comprising:
(a) a substrate; and
(b) a plurality of recombinant herpesviridae virion microspots associated with a surface of the substrate, wherein the recombinant herpesviridae virion microspots comprise a plurality of recombinant herpesviridae virions, wherein the recombinant herpesviridae virions comprise envelopes comprising a plurality of human heterologous membrane bound proteins that retain their native conformations, interactions, or both, and wherein the human heterologous membrane bound proteins are encoded by the genomes of the recombinant herpesviridae virions.

2. The array of claim 1 , wherein the recombinant herpesviridae virions comprise recombinant Herpes simplex virus (HSV) virions.

3. The array of claim 2 , wherein the recombinant HSV virions comprise Herpes simplex virus 1 (HSV-1) virions.

4. The array of claim 1 , wherein the plurality of human heterologous membrane bound proteins comprises a classical type I membrane protein with a single transmembrane domain.

5. The array of claim 4 , wherein the classical type I membrane protein with a single transmembrane domain comprises CD4.

6. The array of claim 1 , wherein the human heterologous membrane bound proteins comprise a multi-spanning G-protein coupled receptor (GPCR) membrane protein.

7. The array of claim 6 , wherein the multi-spanning GPCR membrane protein comprises GPR77.

8. The array of claim 1 , wherein the plurality of human heterologous membrane bound proteins comprises a protein selected from the group consisting of an ion channel, a receptor tyrosine kinase, a receptor serine/threonine kinase, a receptor guanylate cyclase, a growth factor receptor, a hormone receptor, and combinations thereof.

9. The array of claim 1 , wherein a density of the plurality of recombinant herpesviridae virion microspots associated with the surface of the substrate ranges from 1/cm 2 to 50/cm 2 .

10. A method for producing an array comprising a substrate, the method comprising:
(a) contacting a solution comprising recombinant herpesviridae virions to a surface of the substrate, wherein the recombinant herpesviridae virions comprise envelopes comprising a plurality of human heterologous membrane bound proteins, wherein the plurality of human heterologous membrane bound proteins retain their native conformations, interactions, or both, and wherein the human heterologous membrane bound proteins are encoded by the genomes of the recombinant herpesviridae virions; and
(b) repeating the contacting to provide a recombinant herpesviridae virion microspots pattern on the surface of the substrate.

11. The method of claim 10 , wherein the recombinant herpesviridae virions comprise recombinant Herpes simplex virus (HSV) virions.

12. The method of claim 11 , wherein the recombinant HSV virions comprise Herpes simplex virus 1 (HSV-1) virions.

13. The method of claim 10 , wherein the human heterologous membrane bound proteins comprise a classical type I membrane protein with a single transmembrane domain.

14. The method of claim 13 , wherein the classical type I membrane protein with a single transmembrane domain comprises CD4.

15. The method of claim 10 , wherein the human heterologous membrane bound proteins comprise a multi-spanning G-protein coupled receptor (GPCR) membrane protein.

16. The method of claim 15 , wherein the multi-spanning GPCR mebrane protein comprises GPR77.

17. The method of claim 10 , wherein at least one or each of the human heterologous membrane bound proteins is selected from the group consisting of an ion channel, a receptor tyrosine kinase, a receptor serine/threonine kinase, a receptor guanylate cyclase, a growth factor receptor, a hormone receptor, and combinations thereof.

18. A method for detecting a binding event between a human heterologous membrane bound protein and a target, the method comprising:
(a) contacting a sample with the array of claim 1 , wherein the sample comprises a solution comprising the target; and
(b) detecting a binding event between the human heterologous membrane bound protein and the target.

19. The method of claim 18 , wherein the target is labeled and the detecting comprises detecting the presence of the label.

20. The method of claim 19 , wherein the detecting is by optical detection methods comprising absorption in the visible or infrared range, chemoluminescence, fluorescence, optical waveguides, surface plasmon resonance, surface charge sensors, surface force sensors, or combinations thereof.

21. A method of identifying a ligand as a target for a membrane bound protein, the method comprising:
(a) contacting the array of claim 1 with a ligand;
(b) determining binding between a human heterologous membrane bound protein and the ligand; and
(c) identifying the ligand as a target for the membrane bound protein when the human heterologous membrane bound protein binds to the ligand.

22. The method of claim 21 , wherein the ligand is selected from the group consisting of peptides, lipids, fatty acids, carbohydrates, small molecules, and combinations thereof.

23. The method of claim 21 , wherein the ligand comprises a label.

24. The method of claim 23 , wherein the label is selected from the group consisting of fluorescent dyes and radioisotopes.

25. The method of claim 23 , wherein the label is a fluorescent dye selected from the group consisting of Fluo8, DiBAC4, and ANG-2.

Assignees

• Univ Johns Hopkins

Inventors

• Zhu Heng
• Desai Prashant
• Li Min
• Hu Shaohui

Classifications

• C40B40/02

  Libraries contained in or displayed by microorganisms, e.g. bacteria or animal cells; Libraries contained in or displayed by vectors, e.g. plasmids; Libraries containing only microorganisms or vectors · CPC title

• C12N15/1093

  General methods of preparing gene libraries, not provided for in other subgroups · CPC title

• A61B17/3478

  Endoscopic needles, e.g. for infusion (biopsy needles A61B10/0233; catheters with injection needles A61M25/0067) · CPC title

• C07K2319/735

  containing a domain for self-assembly, e.g. a viral coat protein (includes phage display) · CPC title

• C12N2810/855

  from receptors; from cell surface antigens; from cell surface determinants · CPC title