IP Library Granted Patent US 9,944,923
Granted Patent B2
US 9,944,923 · App. 14/897,177 · Granted Apr 17, 2018

Methods for obtaining information from single cells within populations using DNA origami nanostructures without the need for single cell sorting

Inventors: Joseph Blattman (Scottsdale, AZ); Hao Yan (Chandler, AZ); Louis Schoettle (Tempe, AZ); Xixi Wei (Mesa, AZ)
Assignee: Arizona Board of Regents on Behalf of Arizona State University
C12N15/1062C12Q1/6806C12Q1/6816C12Q1/6881B82Y5/00B82Y15/00C12Q2600/16
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Quick Facts
Patent No.
US 9,944,923
App. No.
14/897,177
Granted
Apr 17, 2018
Kind
B2
Abstract

Methods for construction of DNA origami nanostructures, as well as for binding, isolation, linking, and deep sequencing information, such as both of TCR alpha and beta CDR3 mRNA, from individual cells within a mixed population of cells without the need for single cell sorting.

Claims (18)

1. A method for sequencing genetic information from individual cells within a mixed population of cells without single-cell sorting, comprising the steps of:

(a) transfecting a cell with a DNA origami nanostructure;

(b) isolating said DNA origami nanostructure from said transfected cell, wherein the DNA origami nanostructure is bound to complementary RNA from said cell;

(c) reverse transcribing said RNA into complementary DNA (cDNA); and

(d) sequencing said complementary DNA.

2. A method for obtaining both TCR alpha and beta CDR3 mRNA sequences from individual cells within a mixed population of cells without single-cell sorting, comprising the steps of:

(a) transfecting a primary T cell with a DNA origami nanostructure having a sequence complementary to TCR alpha and beta constant region mRNA;

(b) isolating said DNA origami nanostructure from said transfected cell, wherein the DNA origami nanostructure is bound to said sequences of complementary mRNA from said cell;

(c) reverse transcribing said mRNA into complementary DNA (cDNA); and

(d) sequencing said complementary DNA.

3. The method of claim 2 , wherein said DNA origami nanostructures are composed of ssDNA M13 phage refolded with complementary ssDNA staple sequences into predetermined shapes with selected staples extended with complementary sequences to TCR alpha and beta constant region mRNA.

4. The method of claim 1 , wherein said step of transfecting comprises electroporation.

5. A method for sequencing two or more nucleic acid sequences from individual cells within a mixed population of cells without single-cell sorting, comprising the steps of:

(a) transfecting a cell with a DNA origami nanostructure;

(b) isolating said DNA origami nanostructure from said transfected cell, wherein the DNA origami nanostructure is bound to two or more sequences of complementary nucleic acids from said cell; and

(c) sequencing said two or more sequences of complementary nucleic acids.

6. The method of claim 5 , further comprising linking said two or more sequences of complementary nucleic acids into a single DNA molecule and sequencing said DNA.

7. The method of claim 5 , wherein said step of transfecting comprises electroporation.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 11, 2015
From: BLATTMAN, JOSEPH; YAN, HAO; SCHOETTLE, LOUIS; WEI, XIXI
To: ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY
Reel/Frame 037273/0165 →
Continuity (2)
Provisional Application 61834270 · Jun 12, 2013
Related Publication 20160122752A1 · May 5, 2016