Granted Patent B2

US 12,708,677 · App. 18/346,503 · Granted Aug 18, 2026

Inventors: Jenny Jie Yang (Marietta, GA); Zhiren Liu (Atlanta, GA); Jie Jiang (Atlanta, GA); Shenghui Xue (Atlanta, GA); Jinjuan Qiao (Atlanta, GA); Mani Salarian (Decatur, GA)

Assignee: Georgia State University Research Foundation, Inc.

A61K49/14A61K49/126A61K49/143

Abstract

Claims (21)

1 . A contrast agent comprising a modified parvalbumin scaffold polypeptide, wherein one or more amino acids of the scaffold polypeptide form at least one paramagnetic metal ion chelating site, and further comprising a paramagnetic metal ion bound to at least two of the amino acids forming the at least one paramagnetic metal ion chelating site,

wherein the modified parvalbumin scaffold polypeptide has at least one amino acid substitution that modifies at least one of the metal selectivity of the binding site, increases binding affinity for the metal, or increases serum stability of the contrast agent, and wherein the at least one amino acid substitution is selected from the group consisting of S56D, E60D, G99D, and F103W, wherein the amino acid positions are numbered according to SEQ ID NO: 38, and

wherein the paramagnetic metal ion is Mn(II).

2 . The contrast agent of claim 1 , wherein the modified parvalbumin scaffold polypeptide has an amino acid sequence having at least 90% similarity to any of SEQ ID Nos: 28-38.

3 . The contrast agent of claim 1 , wherein the modified parvalbumin scaffold polypeptide has an amino acid sequence selected from the group consisting of SEQ ID Nos: 28-38.

4 . The contrast agent of claim 1 , including at least one post-translational modification.

5 . The contrast agent of claim 1 , further comprising at least one polyethylene glycol (PEG) group or glucan group attached to the modified parvalbumin scaffold polypeptide.

6 . The contrast agent of claim 5 , wherein the PEG has a molecular weight of about 1 to 100 kDa.

7 . The contrast agent of claim 5 , wherein the PEG is attached to the modified parvalbumin scaffold polypeptide via a lysine, a glutamic acid, an aspartic acid, a cysteine, the polypeptide carboxy-terminus, the polypeptide amino-terminus, or a combination thereof.

8 . The contrast agent of claim 1 , wherein at least two metal ion chelating sites are comprised of amino acids of the modified parvalbumin scaffold polypeptide, and wherein each of the metal ion chelating sites has a paramagnetic ion independently bound thereto.

9 . The contrast agent of claim 1 , wherein at least one metal ion chelating site is at least substantially embedded within the modified parvalbumin scaffold polypeptide.

10 . The contrast agent of claim 1 , further comprising a targeting agent attached to the polypeptide.

11 . The contrast agent of claim 10 , wherein the targeting agent targets to Her-2, EGFR, GRPR, integrin, or collagen.

12 . The contrast agent of claim 10 , wherein the targeting agent targets to VEGFR.

13 . A method of imaging a sample comprising:

contacting a sample with a composition comprising the contrast agent of claim 1 ;

introducing the sample contacted with the composition to an imaging system;

detecting a signal generated by or from the contrast agent of the introduced sample; and

generating an image of the sample from the signal.

14 . The method of claim 13 , wherein the modified parvalbumin scaffold polypeptide comprises an amino acid sequence selected from the group consisting of SEQ ID Nos: 28-38.

15 . The method of claim 13 , wherein the imaging system is a PET system.

Assignments (1)

Continuity (5)

References Cited (87)