IP Library Granted Patent US 10,415,040
Granted Patent B2
US 10,415,040 · App. 15/321,644 · Granted Sep 17, 2019

Nucleic acid amphiphiles and nanostructures

Inventors: Efrosini Kokkoli (Minneapolis, MN); Timothy R. Pearce (Minneapolis, MN); Huihui Kuang (Minneapolis, MN)
Assignee: Regents of the University of Minnesota
C12N15/115A61K9/0092A61K47/26A61K47/6925B82Y5/00B82Y30/00B82Y40/00C12N2310/16C12N2310/3515
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,415,040
App. No.
15/321,644
Granted
Sep 17, 2019
Kind
B2
Abstract

Provided herein are nucleic acid amphiphiles and nanostructures such as nanotubes twisted nanotapes and helical nanotapes that comprise the amphiphiles as well as methods to deliver therapeutic agents with the nanostructures.

Claims (54)

1. A self-assembled nanotube comprising a nucleic acid amphiphile of formula I:

A-B-C-D   I

wherein:

A has the formula:

wherein:

each A 1 is independently a saturated or unsaturated (C 5 -C 30 ) hydrocarbon chain;

A 2 is a saturated or unsaturated (C 5 -C 25 ) hydrocarbon chain wherein one or more of the carbon atoms of the hydrocarbon chain is replaced independently with an —O—, —S—, N or —NR—group and wherein one or more of the carbon atoms of the hydrocarbon chain is optionally substituted independently with an oxo or thioxo group, and wherein each R is independently an H, saturated (C 1 -C 10 ) hydrocarbon chain or unsaturated (C 2 -C 10 ) hydrocarbon chain; and

n is 1, 2, 3 or 4;

B is a saturated or unsaturated (C 10 -C 16 ) hydrocarbon chain wherein 1 or 2 of the carbon atoms of the hydrocarbon chain is replaced independently with an —O—, —S or —NR— group and wherein 1 or 2 of the carbon atoms of the hydrocarbon chain is optionally substituted independently with an oxo or thioxo group, and wherein each R is independently H, saturated (C 1 -C 10 ) hydrocarbon chain or unsaturated (C 2 -C 10 ) hydrocarbon chain, or B is absent provided that when B is absent, the polynucleotide comprises one or more guanine nucleotides and is greater than 10 nucleotides in length;

C is absent, or C is a saturated or unsaturated (C 2 -C 10 )hydrocarbon chain; and

D is single stranded DNA comprising 5-50 nucleotides or a single stranded RNA comprising 5-50 nucleotides;

or a salt thereof; and

provided that D is not the nucleotide sequence

(SEQ ID NO: 2)

GGGGTGGGTGGGGGGCACGTGTGGGGGCGGCCAGGGTGCT.

2. The nanotube of claim 1 , wherein each A 1 is independently a saturated or unsaturated (C 10 -C 30 ) hydrocarbon chain.

3. The nanotube of claim 1 wherein A is

4. The nanotube of claim 1 , wherein B is a saturated or unsaturated (C 10 -C 16 ) hydrocarbon chain wherein 1 or 2 of the carbon atoms of the hydrocarbon chain are replaced independently with an —O—, —S or —NR— group and wherein 1 or 2 of the carbon atoms of the hydrocarbon chain are substituted independently with an oxo or thioxo group, and wherein each R is independently H, saturated (C 1 -C 10 ) hydrocarbon chain or unsaturated (C 2 -C 10 ) hydrocarbon chain.

5. The nanotube of claim 1 , wherein B is

6. The nanotube of claim 1 wherein C is a saturated or unsaturated (C 2 -C 10 )hydrocarbon chain.

7. The nanotube of claim 1 , wherein D is selected from the group consisting of:

(SEQ ID NO: 4)

5′-TTCTATTCTC-3′;

(SEQ ID NO: 5)

5′-CCAATTAATT-3′;

(SEQ ID NO: 6)

5′-TTCTATTCTCACATTTCATCTATTA-3′;

(SEQ ID NO: 7)

5′-TTCTATTCTCACATTTCATCTATTAAACCACCAATTAATT-3′;

(SEQ ID NO: 3)

5′-GGGGGTTCTC-3′;

(SEQ ID NO: 8)

5′-GGGGGTAATT-3′;

(SEQ ID NO: 9)

5′-GGGGGTTCTCACATTTCATCTATTA-3′;

(SEQ ID NO: 10)

5′-GGGGGTTCTCACATTTCATCTATTAAACCACCAATTAATT-3′;

(SEQ ID NO: 11)

5′-GGGTGGGTGGGTATTTCATCTATTA-3′;

(SEQ ID NO: 12)

5′-GGGTGGGTGGGTATTTCATCTATTAAACCACCAATTAATT-3′;

(SEQ ID NO: 13)

5′-GGGTGGGTGGGTGGGTCATCTATTA-3′;

(SEQ ID NO: 14)

5′-GGTGGTGGTGGTATTTCATCTATTA-3′;

(SEQ ID NO: 15)

5′-GGGTGGGTGGGTGGGTCATCTATTAAACCACCAATTAATT-3′

and

(SEQ ID NO: 16)

5′-CCCTATTCCCAGATCCCATTACCC-3′.

8. A pharmaceutical composition comprising a nanotube as described in claim 1 or a pharmaceutically acceptable salt thereof and a pharmaceuticaly acceptable carrier.

9. The nanotube of claim 1 wherein A 2 is a saturated (C 10 -C 20 ) hydrocarbon chain wherein 1, 2, 3, 4, 5, 6, 7 or 8 of the carbon atoms of the hydrocarbon chain is replaced independently with an —O—, —S—, N or —NR— group and wherein 1, 2, 3, 4, 5, 6, 7 or 8 of the carbon atoms of the hydrocarbon chain is substituted independently with an oxo or thioxo group, and wherein each R is independently an H, saturated (C 1 -C 10 ) hydrocarbon chain or unsaturated (C 2 -C 10 ) hydrocarbon chain.

10. The nanotube of claim 1 wherein A 2 is a saturated (C 10 -C 16 ) hydrocarbon wherein 1, 2, 3, 4, 5 or 6 of the carbon atoms of the hydrocarbon chain is replaced independently with an —O—, —S or —NR— group and wherein 1, 2, 3, 4, 5 or 6 of the carbon atoms of the hydrocarbon chain is substituted independently with an oxo or thioxo group, and wherein each R is independently an H, saturated (C 1 -C 10 ) hydrocarbon chain or unsaturated (C 2 -C 10 ) hydrocarbon chain.

11. The nanotube of claim 1 wherein each A 1 is independently a saturated (C 10 -C 25 ) hydrocarbon chain.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 5, 2019
From: PEARCE, TIMOTHY R.
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 049960/0624 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 1, 2019
From: KOKKOLI, EFROSINI; KUANG, HUIHUI
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 049937/0662 →
CONFIRMATORY LICENSE Recorded Feb 15, 2017
From: UNIVERSITY OF MINNESOTA
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 041726/0968 →
Continuity (2)
Provisional Application 62016045 · Jun 23, 2014
Related Publication 20170218367A1 · Aug 3, 2017