IP Library Granted Patent US 7,598,363
Granted Patent B2
US 7,598,363 · App. 11/148,423 · Granted Oct 6, 2009

Polygonal nanostructures of polynucleic acid multi-crossover molecules and assembly of lattices based on double crossover cohesion

Assignee: New York University
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Quick Facts
Patent No.
US 7,598,363
App. No.
11/148,423
Granted
Oct 6, 2009
Kind
B2
Abstract

Robust nucleic acid arrays and lattices are assembled based on double crossover cohesion of polygonal units whose edges are composed of nucleic acid multi-crossover domains.

Claims (34)

1. A polynucleic acid structure, comprising a polygonal unit whose edges are parallel helices of connected nucleic acid multi-crossover domains along their helix axes, each of said edges having at least one free end with two parallel helices, wherein each of said two parallel helices at one free end of each of said edges terminate in a cohesive end to provide a double cohesive end on said one free end.

2. The polynucleic acid structure of claim 1 , wherein said nucleic acid multi-crossover domains are double crossover domains.

3. The polynucleic acid structure of claim 1 , wherein said nucleic acid multi-crossover domains are triple crossover domains.

4. The polynucleic acid structure of claim 1 , wherein said polygonal unit is a triangle.

5. The polynucleic acid structure of claim 1 , wherein said polygonal unit is a parallelogram.

6. The polynucleic acid structure of claim 1 , wherein each of said edges has a single free end with two parallel helices, and each of said two parallel helices at said single free end terminate in a cohesive end to provide a double cohesive end on each of said single free end.

7. The polynucleic acid structure of claim 1 , wherein each of said edges has two free ends, each with two parallel helices, and each of said parallel helices of said free ends terminate in a cohesive end to provide double cohesive ends on said free ends.

8. The polynucleic acid structure of claim 1 , wherein the cohesive ends on said two parallel helices are different.

9. The polynucleic acid structure of claim 1 , wherein:

said polygonal unit is a triangle having as edges connected nucleic acid double crossover domains;

each of said edges has a single free end with two parallel helices; and

each of said two parallel helices at said single free end terminate in a cohesive end to provide a double cohesive end on said single free end.

10. The polynucleic acid structure of claim 1 , wherein:

said polygonal unit is a triangle having as edges connected nucleic acid triple crossover domains;

each of said edges has two free ends each with two parallel helices; and

each of said two parallel helices terminate in a cohesive end to provide double cohesive ends on each of said free ends.

11. The polynucleic acid structure of claim 1 , wherein:

said polygonal unit is a parallelogram having as edges nucleic acid double crossover domains;

each of said edges has two free ends each with two parallel helices; and

each of said two parallel helices terminate in a cohesive end to provide double cohesive ends on each of said free ends.

12. The polynucleic acid structure of claim 1 , which is an array of polygonal units linked together by complementary double cohesive ends.

13. The polynucleic acid structure of claim 12 , wherein said array is an array of triangular units linked together by complementary double cohesive ends to form a trigonal lattice.

14. The polynucleic acid structure of claim 12 , which is an array of two different triangular units linked together by complementary double cohesive ends to form a trigonal lattice.

15. The polynucleic acid structure of claim 12 , wherein said array is an array of parallelogram units linked together by complementary double cohesive ends.

16. A method for producing the polynucleic acid structure of claim 1 , comprising:

synthesizing single stranded polynucleotides, each being designed to be self-complementary and/or complementary to another single stranded polynucleotide so as to be capable of self-annealing into a polygonal unit;

mixing the single stranded polynucleotides to form a mixture of polynucleotides and heat denaturing the mixture; and

annealing the heat denatured mixture of single stranded polynucleotides to form the polygonal unit by self-assembly.

17. The method of claim 16 , further comprising:

heating the annealed polygonal unit to ensure exposed cohesive ends; and

annealing exposed complementary cohesive ends of a plurality of the annealed polygonal unit to form an array of polygonal units.

18. The method of claim 16 , wherein two different polygonal units are separately formed and wherein the method further comprises:

heating the two different annealed polygonal units to ensure exposed cohesive ends; and

annealing the exposed cohesive ends that are complementary to form an array of two different polygonal units.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 22, 2022
From: NEW YORK UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 060859/0762 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 12, 2005
From: SEEMAN, NADRIAN C.; DING, BAOQUAN; CONSTANTINOU, PAMELA; WANG, TONG; KOPATSCH, JENS; ZHANG, XIAOPING; SHA, RUOJIE; ISRAEL, LISA
To: NEW YORK UNIVERSITY
Reel/Frame 016519/0714 →
Continuity (2)
Provisional Application 6057830600 · Jun 10, 2004
Related Publication 20060078910A1 · Apr 13, 2006