IP Library Granted Patent US 9,771,396
Granted Patent B2
US 9,771,396 · App. 14/572,391 · Granted Sep 26, 2017

Phase transition biopolymers and methods of use

Inventors: Ashutosh Chilkoti (Durham, NC); Felipe Garcia Quiroz (Durham, NC); Miriam Amiram (Chapel Hill, NC)
Assignee: Duke University
C07K14/001A61K8/11A61K8/64A61K9/5123A61K9/5169A61K38/00A61K47/42B82Y5/00C07K14/78C07K19/00C07K2319/00C07K2319/21
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 9,771,396
App. No.
14/572,391
Granted
Sep 26, 2017
Kind
B2
Abstract

The present disclosure describes environmentally responsive polypeptides capable of displaying stimuli-triggered conformational changes in a reversible or irreversible manner that may be accompanied by aggregation. Polypeptides include a number of repeated motifs and may be elastomeric or non-elastomeric. The polypeptides may be used to deliver therapeutics to a biological site and to develop bioactive polypeptides that are environmentally responsive.

Claims (14)

1. An environmentally responsive polypeptide comprising at least ten repeats of at least one sequence selected from VGAPVG (SEQ ID NO: 24), LGAPVG (SEQ ID NO: 25), VPSALYGVG (SEQ ID NO: 26), VGPAVG (SEQ ID NO: 27), VTPAVG (SEQ ID NO: 28), VPSDDYGQG (SEQ ID NO: 29), VPSDDYGVG (SEQ ID NO: 30), TPVAVG (SEQ ID NO: 31), VPSTDYGVG (SEQ ID NO: 32), VPAGVG (SEQ ID NO: 33), VPTGVG (SEQ ID NO: 34), VPAGLG (SEQ ID NO: 35), VPHVG (SEQ ID NO: 36), VHPGVG (SEQ ID NO: 37), VPGAVG (SEQ ID NO: 38), VPGVAG (SEQ ID NO: 39), VRPVG (SEQ ID NO: 40), GRGDSPY (SEQ ID NO: 41), GRGDSPH (SEQ ID NO: 42), GRGDSPV (SEQ ID NO: 43), GRGDSPYG (SEQ ID NO: 44), RPLGYDS (SEQ ID NO: 45), RPAGYDS (SEQ ID NO: 46), RPXGYDS (SEQ ID NO :136), GRGDSYP (SEQ ID NO: 47), GRGDSPYQ (SEQ ID NO: 48), GRGNSPYG (SEQ ID NO: 49), GRGDAPYQ (SEQ ID NO: 50), VPXSRNGG (SEQ ID NO: 137), VPHSRNGG (SEQ ID NO: 51), VPHSRNGL (SEQ ID NO: 52), VPGHSHRDFQPVLHLVALNSPLSGGMRG (SEQ ID NO: 53), HTHQDFQPVLHLVALNTPLSGGMRGIRPGG (SEQ ID NO: 54), and FEWTPGWYQPYG (SEQ ID NO: 55), wherein X is from zero to four amino acid residues, and wherein the polypeptide upon stimulation undergoes a conformational change that is accompanied by aggregation.

2. The polypeptide of claim 1 , wherein the at least ten repeats are in tandem.

3. The polypeptide of claim 1 , further comprising a spacer sequence between at least two of the at least ten sequences.

4. The polypeptide of claim 3 , wherein the spacer sequence comprises from one to twenty-six amino acids.

5. The polypeptide of claim 1 , wherein the polypeptide is responsive to temperature and exhibits phase separation when exposed to a threshold temperature that is (i) above a lower critical solution temperature of the polypeptide, or (ii) below an upper critical solution temperature of the polypeptide, or exhibits phase separation when exposed to a threshold temperature that is above the lower critical solution temperature, and when exposed to a threshold temperature that is below the upper critical solution temperature.

6. The polypeptide of claim 1 , wherein the polypeptide comprises at least ten repeats of at least one sequence selected from VGAPVG (SEQ ID NO: 24), TPVAVG (SEQ ID NO: 31), and VGPAVG (SEQ ID NO: 27), and wherein the polypeptide exhibits heat-irreversible phase separation when exposed to a threshold temperature that is above a lower critical solution temperature of the polypeptide, and exhibits reversible phase separation below the threshold temperature.

7. The polypeptide of claim 1 , wherein the at least 10 sequences convey LCST or UCST transition behavior, and wherein the polypeptide further comprises at least 9 sequences which are interspersed among the at least 10 sequences, wherein the at least 9 sequences convey LCST transition behavior when the at least 10 sequences convey UCST transition behavior, and UCST transition behavior when the at least 10 sequences convey LCST transition behavior, such that the polypeptide displays both LCST and UCST transition behavior.

8. A fusion protein comprising the polypeptide of claim 1 .

9. A composition comprising the polypeptide of claim 1 , conjugated to a molecule.

10. The composition of claim 9 , wherein the molecule is selected from an oligonucleotide, a therapeutic, a carbohydrate, a synthetic polymer, or a combination thereof.

11. A polypeptide comprising the at least ten sequences of the polypeptide of claim 1 as a reverse sequence when read from C-terminus to the N-terminus.

12. A method of effecting a conformational change in a polypeptide comprising exposing the polypeptide of claim 1 to a stimulus such that the polypeptide undergoes a conformational change that is accompanied by aggregation or solubilization in response to the stimulus.

13. The method of claim 12 , wherein the polypeptide becomes bioactive or loses bioactivity following the conformational change.

14. An environmentally responsive polypeptide comprising at least ten PG motifs, and at least nine spacer sequences between the PG motifs, the at least nine spacer sequences being between five and thirty amino acid residues in length and not comprising a PG motif, and wherein the polypeptide upon stimulation undergoes a conformational change that is accompanied by aggregation.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2014
From: CHILKOTI, ASHUTOSH; GARCIA-QUIROZ, FELIPE; AMIRAM, MIRIAM
To: DUKE UNIVERSITY
Reel/Frame 034526/0255 →
Continuity (4)
Division 13904836 · May 29, 2013
Division 13245459 · Sep 26, 2011
Provisional Application 61386002 · Sep 24, 2010
Related Publication 20150112022A1 · Apr 23, 2015