IP Library Granted Patent US 12,187,813
Granted Patent B2
US 12,187,813 · App. 18/167,350 · Granted Jan 7, 2025

Methods of identifying opioid cyclic peptides

Inventors: Predrag Cudic (Boca Raton, FL); Jay McLaughlin (Gainesville, FL)
Assignees: Florida Atlantic University Board of Trustees; University of Florida Research Foundation
C07K5/12A61K9/0043A61K31/4045A61K47/64A61K47/65A61P25/04A61P25/06A61P25/16A61P25/18A61P25/28A61P25/36C07K7/64A61K38/00C40B40/10
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Quick Facts
Patent No.
US 12,187,813
App. No.
18/167,350
Granted
Jan 7, 2025
Kind
B2
Abstract

Novel cyclic peptides, cyclic peptide conjugates and compositions containing them for treating neurological diseases in a subject include an Odorranalectin (OL) sequence or modified OL sequence as a scaffold and a biologically active peptide or protein and/or therapeutic agent conjugated thereto. Methods of treatment of neurological diseases are based on intranasal delivery of a cyclic peptide or cyclic peptide conjugate as described herein. Combinatorial libraries that include a plurality of cyclic peptides have also been developed and can be used to screen for a ligand(s) for a receptor of interest.

Claims (32)

1. A method of identifying opioid cyclic peptides comprising:

i) providing a combinatorial library comprising a plurality of distinct cyclic peptides of the general Formula II:

(SEQ ID NO: 18)

Tyr-Ala-Ser-Pro-Lys-cyclo-[Cys-Phe-Arg-XXXXX-

Leu-Ala-Cys]-Thr,

wherein each X is an amino acid selected from the group consisting of: D-amino acid, L-amino acid, non-natural synthetic amino acid, naturally occurring amino acid, and a mixture thereof;

ii) screening the plurality of cyclic peptides for binding affinity to μ-opioid receptor (MOR), δ-opioid receptor (DOR), and κ-opioid receptor (KOR) in mammalian cells

using a screening assay to identify any cyclic peptide that has binding affinity for at least one opioid receptor a candidate opioid cyclic peptide; and

iii) testing any candidate opioid cyclic peptide using an in vitro or in vivo functional activity assay for agonist effects on the at least one opioid receptor, wherein

any candidate opioid cyclic peptide that has an affinity for at least one opioid receptor and that has agonist effects on the at least one opioid receptor is an opioid cyclic peptide.

2. The method of claim 1 , wherein the at least one opioid receptor is μ-n opioid receptor (MOR).

3. The method of claim 1 , wherein the combinatorial library is a positional-scanning synthetic combinatorial library.

4. The method of claim 1 , wherein the screening assay comprises a competitive binding assay.

5. The method of claim 1 , wherein the at least one opioid receptor is δ-opioid receptor (DOR).

6. The method of claim 1 , wherein the at least one opioid receptor is κ-opioid receptor (KOR).

7. The method of claim 1 , further comprising step iv) comprising administering an opioid cyclic peptide identified in step iii) to an animal and examining effects of the opioid cyclic peptide on respiration and analgesia in the animal.

8. A method of identifying opioid cyclic peptides comprising:

i) providing a combinatorial library comprising a plurality of distinct cyclic peptides of the general Formula II:

(SEQ ID NO: 18)

Tyr-Ala-Ser-Pro-Lys-cyclo-[Cys-Phe-Arg-XXXXX-Leu- 

Ala-Cys]-Thr,

wherein each X is an amino acid selected from the group consisting of: D-amino acid, L-amino acid, non-natural synthetic amino acid, naturally occurring amino acid, and a mixture thereof;

ii) screening the plurality of cyclic peptides for binding affinity to u-opioid receptor (MOR), δ-opioid receptor (DOR), and κ-opioid receptor (KOR) in mammalian cells

using a screening assay to identify any cyclic peptide that has binding affinity for at least one opioid as a candidate opioid cyclic peptide; and

iii) testing any candidate opioid cyclic peptide using an in vitro or in vivo functional activity assay for antagonist effects on the at least one opioid receptor, wherein

any candidate opioid cyclic peptide that has an affinity for at least one opioid receptor and that has antagonist effects on the at least one opioid receptor is an opioid cyclic peptide.

9. The method of claim 8 , wherein the at least one opioid receptor is MOR.

10. The method of claim 8 , wherein the at least one opioid receptor is DOR.

11. The method of claim 8 , wherein the at least one opioid receptor is KOR.

12. The method of claim 8 , wherein the combinatorial library is a positional-scanning synthetic combinatorial library.

13. The method of claim 8 , wherein steps ii) and iii) comprise a competitive binding assay.

14. The method of claim 8 , further comprising step iv) comprising administering an opioid cyclic peptide identified in step iii) to an animal and examining effects of the opioid cyclic peptide on respiration and analgesia in the animal.

Assignments (4)
CONFIRMATORY LICENSE Recorded Aug 3, 2023
From: FLORIDA ATLANTIC UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 064480/0210 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2023
From: CUDIC, PREDRAG; MCLAUGHLIN, JAY
To: FLORIDA ATLANTIC UNIVERSITY BOARD OF TRUSTEES
Reel/Frame 062657/0824 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2023
From: MCLAUGHLIN, JAY
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED
Reel/Frame 062657/0938 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2023
From: FLORIDA ATLANTIC UNIVERSITY BOARD OF TRUSTEES
To: FLORIDA ATLANTIC UNIVERSITY RESEARCH CORPORATION
Reel/Frame 062658/0001 →
Continuity (3)
Division 16257580 · Jan 25, 2019
Provisional Application 62649290 · Mar 28, 2018
Related Publication 20230257418A1 · Aug 17, 2023
References Cited (25)
US 7507875B2 · Bloksberg et al. · 2009 [cited by applicant]
US 7745391B2 · Mintz et al. · 2010 [cited by applicant]
US 8067671B2 · Boukharov et al. · 2011 [cited by applicant]
US 9012723B2 · Guo et al. · 2015 [cited by applicant]
US 10611798B2 · Bar-Shavit · 2020 [cited by applicant]
US 20180222940A1 · Zadina et al. · 2018 [cited by applicant]
Li et all., “Odorranalectin Is a Small Peptide Lectin with Potential for Drug Delivery and Targeting,” PlosOne 3:e2381, pp. 1-10 (2008) (Year: 2008). [cited by examiner]
Wu et al., “A novel small Odorranalectin-bearing cubosomes: Preparation, brain delivery and pharmacodynamic study on amyloid-b25-35-treated rats following intranasal administration,” European Journal of pharmaceutics bi… [cited by examiner]
Mollica et al., “Rational Approach to the Design of Bioactive Peptidomimetics: Recent Developments in Opioid Agonist Peptides,” Natural Products Chemistry46:27-61 (2015) (Year: 2015). [cited by applicant]
Martin, et al. “Neurodegenation in excitotoxcity, global cerebral ischemia, and target deprivation: A perspective on the contributions of aptopsis and necrosis,” Brain Res. Bull, 46:281-309 (1998) (Year: 1998). [cited by applicant]
Korczyn, A.D. and Nussbaum, M., “Emerging Therapies in the Pharmacological Treatment of Parkinson's Disease,” Drugs 62:775-786 (2002) (Year: 2002). [cited by applicant]
Schiller et al., “Differential stereochemical requirements of mu vs. delta opioid receptors for ligand binding and signal transduction: Development of a class of potent and highly delta-selective peptide antagonists”, P… [cited by applicant]
Wen et al., “Odorranalectin-conjugated nanoparticles: Preparation, brain delivery and pharmacodynamic study on Parkinson's disease following intranasal administration”, Journal of Controlled Release, Feb. 2011, vol. 151… [cited by applicant]
Gianolio et al., “Hyaluronan-Tethered Opioid Depots: Synthetic Strategies and Release Kinetics In Vitro and In Vivo”, American Chemical Society, Jul. 2008, vol. 19, pp. 1767-1774. [cited by applicant]
Schiller et al., “The TIPP Opioid Peptide Family: Development of delta Antagonists, delta Agonists, and Mixed mu Agonist/delta Antagonists”, Biopolymers (Peptide Science), 1999, vol. 51, pp. 411-425. [cited by applicant]
Tang et al., ““Click” reactions: a versatile toolbox for the synthesis of peptide-conjugates”, Chemical Society Reviews, Jul. 2014, vol. 43, No. 20, pp. 7013-7039. [cited by applicant]
Oluigbo et al., IEEE Reviews in Biomedical Engineering, vol. 5, 2012, 88-99. (Year: 2012). [cited by applicant]
Zealand Pharma A/S, What are peptides, at URL www.zealandpharma.com/what-are-peplides, accessed May 7, 2021. (Year: 2021). [cited by applicant]
Benavente, “Cell surface glycan-lectin interactions for biomedical applications,” PHD Thesis dissertation, Florida Atlantic University, 2015—accessed at URL fau.digital.flvc.org/islandora/objecl/fau%3A31323. (Year: 2015… [cited by applicant]
Shaw et al., “Tryptophan and 5-Hydroxy 1ryptophan for depression.” Cochrane Database of Systematic Reviews Iss. 1, pp. 1-18 (2010) (Year: 2010). [cited by applicant]
Margolis , R. “Diagnosis of Huntington's Disease,” Clin. Chem. 49:1726-32 (2003) (Year: 2003). [cited by applicant]
Compston, et al. “Mutliple Sclerosis,” The Lancet 359:1221-1231 (2002) (Year: 2002). [cited by applicant]
Pain, Merck Manual, accessed Oct. 14, 2023 at URL merckmanuals.com/professional/neurologic-disorders/pain/overview-of-pain, pp. 1-3. [cited by applicant]
Treatment of pain, Merck Manual, accessed Oct. 14, 2023 at URL merckmanuals.com/professional/neurologic-disorders/pain/treatment, pp. 1-17. [cited by applicant]
Goodman, “Neurobiology of addiction- and integrative review,” biochemical pharmacology 75:266-322 (2008) (Year: 2008). [cited by applicant]