IP Library Granted Patent US 8,617,516
Granted Patent B2
US 8,617,516 · App. 12/910,385 · Granted Dec 31, 2013

Universal anchor peptide for nanoparticles

Inventors: Samuel A. Wickline (St. Louis, MO); Hua Pan (St. Louis, MO); Neelesh R. Soman (St. Louis, MO); Gregory M. Lanza (St. Louis, MO); Paul H. Schlesinger (St. Louis, MO)
Assignee: Washington University
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Quick Facts
Patent No.
US 8,617,516
App. No.
12/910,385
Granted
Dec 31, 2013
Kind
B2
Abstract

The present invention provides a substantially non-lytic, non-cytotoxic anchor peptide that is capable of stably inserting into lipid membranes. In particular, the invention provides nanoparticles comprising stably inserted anchor peptides, which may be conjugated to a variety of different cargo complexes.

Claims (8)

1. A nanoparticle, the nanoparticle comprising a core encapsulated by a lipid layer, the lipid layer comprising a stably inserted anchor peptide, wherein the anchor peptide is substantially non-lytic, non-cytotoxic, consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:5-218, and has an association rate of at least about 9×10 5 M −1 s −1 and a dissociation constant of less than about 1×10 −6 M.

2. The nanoparticle in of claim 1 , wherein the anchor peptide consists of SEQ ID NO:88.

3. The nanoparticle of claim 1 , wherein the anchor peptide is conjugated to at least one cargo complex selected from the group consisting of an imaging cargo, a therapeutic cargo, a cytotoxic cargo, and a targeting cargo.

4. A kit for preparing a nanoparticle comprising an anchor peptide, the kit comprising a first composition and a second composition, the first composition comprising a nanoparticle comprising a core encapsulated by a lipid layer, the second composition comprising the anchor peptide which is substantially non-lytic, non-cytotoxic, consists of an amino acid sequence selected from the group consisting of SEQ ID NOs:5-218, and has an association rate of at least about 9×10 5 M −1 s −1 and a dissociation constant of less than about 1×10 −6 M.

5. The kit of claim 4 , wherein the anchor peptide consists of SEQ ID NO:88.

6. The kit of claim 4 , wherein the anchor peptide is conjugated to a cargo complex selected from the group consisting of an imaging cargo, a therapeutic cargo, a cytotoxic cargo, and a targeting cargo.

7. A method for adding a cargo complex to a nanoparticle comprising a lipid layer, the method comprising contacting the nanoparticle with an anchor peptide that is conjugated to the cargo complex, the anchor peptide being substantially non-lytic, non-cytotoxic, and consisting of an amino acid sequence selected from the group consisting of SEQ ID NOs:5-218 with an association rate of at least about 9×10 5 M −1 s −1 and a dissociation constant of less than about 1×10 −6 M, wherein the anchor peptide stably inserts into the lipid layer of the nanoparticle.

8. The method of claim 7 , wherein the cargo complex is selected from the group consisting of an imaging cargo, a therapeutic cargo, a cytotoxic cargo, and a targeting cargo.

Assignments (3)
CONFIRMATORY LICENSE Recorded Mar 31, 2017
From: WASHINGTON UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042125/0740 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 21, 2011
From: WICKLINE, SAMUEL A., MD; SOMAN, NEELESH RAMCHANDRA; PAN, HUA; SCHLESINGER, PAUL H., PHD; LANZA, GREGORY
To: WASHINGTON UNIVERSITY
Reel/Frame 025838/0005 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2011
From: WICKLINE, SAMUEL A., MD; SOMAN, NEELESH RAMCHANDRA; PAN, HUA; SCHLESINGER, PAUL H., PHD
To: WASHINGTON UNIVERSITY
Reel/Frame 025735/0142 →
Continuity (3)
Continuation In Part PCTUS2009041000 · Apr 17, 2009
Provisional Application 61047013 · Apr 22, 2008
Related Publication 20110123438A1 · May 26, 2011