US2023212252A1PendingUtilityA1
RAGE Fusion Proteins with Improved Stability and Ligand Binding Affinity and Uses Thereof
Est. expirySep 14, 2038(~12.2 yrs left)· nominal 20-yr term from priority
C07K 14/70503C07K 2319/30A61P 3/10A61K 38/00C07K 2319/02
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Claims
Abstract
The present invention provides soluble RAGE-Fc fusion proteins with increased stability and extended half-life capable of binding endogenous RAGE ligands with high apparent affinity. The present invention also provides methods of making and using stable, soluble RAGE-Fc fusion proteins. These soluble RAGE-Fc fusion proteins are useful as therapeutics based on their ability to bind endogenous RAGE ligands.
Claims
exact text as granted — not AI-modified1 . An isolated polynucleotide encoding a polypeptide comprising:
(a) a first domain having an amino acid sequence at least 97% identical to the sequence of SEQ ID NO:74; and (b) a second domain comprising a fragment of a Fc region of an immunoglobulin,
wherein the carboxy terminus of said first domain is coupled to the amino terminus of said second domain by a peptide linkage, and
wherein the polypeptide comprising the first domain and the second domain has an amino acid sequence selected from: SEQ ID NO: 12, SEQ ID NO:15, SEQ ID NO: 16, and SEQ ID NO: 53.
2 . The isolated polynucleotide of claim 1 , wherein said polypeptide is resistant to cleavage by a disintegrin and metalloproteinase 10 (ADAM10).
3 . The isolated polynucleotide of claim 1 , wherein said polypeptide is at least 15% more resistant to cleavage by at least one of ADAM10, matrix metalloproteinase 9 (MMP9), and trypsin as compared to a polypeptide having the sequence of SEQ ID NO: 5.
4 . The isolated polynucleotide of claim 1 , wherein said polypeptide is at least 15% more resistant to degradation in human serum as compared to a polypeptide comprising the sequence of SEQ ID NO: 5, wherein the percent resistance equals the difference between the fraction of peptide that remains full length following incubation in human serum for a defined time period compared to a control peptide treated for the same time and under the same conditions.
5 . The isolated polynucleotide of claim 1 , wherein said polypeptide has increased thermal stability of at least 5° C. as compared to a polypeptide having the sequence of SEQ ID
6 . The isolated polynucleotide of claim 1 , wherein said polypeptide specifically binds an advanced glycation endproduct (AGE).
7 . The isolated polynucleotide of claim 1 , wherein said polypeptide specifically binds HMGB1 (Amphoterin).
8 . The isolated polynucleotide of claim 1 , wherein said polypeptide specifically binds at least one of the group consisting of: S100A1, S100A2, S100A4 (metastasin), S100A5, S100A6, S100A7 (psoriasin), S100A8/9, S100A11, S100A12, S100B, S100P, lipopolysaccharide (LPS), oxidized low-density lipoprotein (oxLDL), CD11b (MAC1), phosphatidyl serine, C3a, S100P, S100G, S100Z, carbonylated proteins, malondialdehyde (MDA), laminin, type I Collagen, type IV Collagen, CAPZA1, CAPZA2, DDOST, LGALS3, MAPK1, MAPK3, PRKCSH, S100A4, S100A5, S100A6, S100A8, S100A9, S100P, and SAA1.
9 . The isolated polynucleotide of claim 1 , wherein said polypeptide specifically binds amyloid-beta.
10 . The isolated polynucleotide of claim 1 , wherein said first domain comprises at least one asparagine residue linked to a glycan.
11 . The isolated polynucleotide of claim 1 , wherein said first domain has the sequence set forth in SEQ ID NO: 74.
12 . The isolated polynucleotide of claim 1 , wherein said Fc fragment comprises CH2 and CH3 domains of a human IgG.
13 . The isolated polynucleotide of claim 1 , wherein the isolated polynucleotide comprises a nucleotide sequence selected from SEQ ID NO: 39, SEQ ID NO: 41, SEQ ID NO: 43, and SEQ ID NO: 56.
14 . An isolated polynucleotide encoding a fusion protein, the isolated polynucleotide comprising:
a nucleotide sequence selected from SEQ ID NO: 39, SEQ ID NO: 41, SEQ ID NO: 43, and SEQ ID NO: 56.
15 . A vector comprising the isolated polynucleotide of claim 14 .
16 . A host cell comprising the isolated polynucleotide of claim 14 .
17 . The host cell comprising the vector of claim 15 .
18 . The host cell of claim 16 , wherein the host cell is a mammalian cell.Join the waitlist — get patent alerts
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