IP Library Granted Patent US 10,961,287
Granted Patent B2
US 10,961,287 · App. 15/887,313 · Granted Mar 30, 2021

Extended recombinant polypeptides and compositions comprising same

Inventors: Volker Schellenberger (Palo Alto, CA); Joshua Silverman (Los Altos Hills, CA); Chia-wei Wang (Santa Clara, CA); Benjamin Spink (San Carlos, CA); Willem P. Stemmer (Los Gatos, CA); Nathan Geething (Natick, MA); Wayne To (Fremont, CA); Jeffrey L. Cleland (San Carlos, CA)
Assignee: Amunix Pharmaceuticals, Inc
C07K14/47C07K14/001C07K14/545C07K14/605C07K14/61C07K14/745C12N9/644C12N9/6437C07K2319/31C07K2319/35
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Quick Facts
Patent No.
US 10,961,287
App. No.
15/887,313
Granted
Mar 30, 2021
Kind
B2
Abstract

The present invention relates to compositions comprising biologically active proteins linked to extended recombinant polypeptide (XTEN), isolated nucleic acids encoding the compositions and vectors and host cells containing the same, and methods of using such compositions in treatment of glucose-related diseases, metabolic diseases, coagulation disorders, and growth hormone-related disorders and conditions.

Claims (24)

1. An extended recombinant polypeptide (XTEN), wherein the XTEN comprises a motif selected from the group consisting of SEQ ID NO: 186, SEQ ID NO: 187, SEQ ID NO: 188, and SEQ ID NO: 189, wherein when linked to a biologically active protein, said biologically active protein is not a coagulation factor.

2. The XTEN of claim 1 , wherein the sum of glycine (G), alanine (A), serine (S), threonine (T), glutamate (E), and proline (P) residues constitutes more than about 80% of the total amino acid sequence of the XTEN.

3. The XTEN of claim 2 , wherein the total amino acid sequence of the XTEN is substantially non-repetitive such that (i) the XTEN sequence contains no three contiguous amino acids that are identical unless the amino acids are serine residues, or (ii) at least 80% of the XTEN sequence comprises non-overlapping sequence motifs, each of the sequence motifs comprising 12 amino acid residues, wherein any two contiguous amino acid residues do not occur more than twice in each of the sequence motifs.

4. The XTEN of claim 3 , wherein

(a) the sum of asparagine and glutamine residues is less than 10% of the total amino acid sequence of the XTEN;

(b) the sum of methionine and tryptophan residues is less than 2% of the total amino acid sequence of the XTEN; and

(c) no one type of amino acid constitutes more than 30% of the XTEN sequence.

5. The XTEN of claim 1 , wherein the XTEN comprises an amino acid sequence that is at least 90% identical to SEQ ID NO: 204, 206, 210, 213, or 217.

6. The XTEN of claim 1 , wherein the XTEN comprises an amino acid sequence that is at least 95% identical to SEQ ID NO: 204, 206, 210, 213, or 217.

7. The XTEN of claim 1 , wherein the XTEN comprises an amino acid sequence that is identical to SEQ ID NO: 204, 206, 210, 213, or 217.

8. An isolated fusion protein comprising the XTEN of claim 1 linked to the biologically active protein that is not a coagulation factor.

9. The isolated fusion protein of claim 8 , further comprising a second XTEN sequence.

10. The isolated fusion protein of claim 8 , further comprising a spacer sequence between the biologically active protein and the XTEN, wherein the spacer sequence is between 1 and 50 amino acid residues in length.

11. The isolated fusion protein of claim 10 , wherein the spacer further comprises a cleavage sequence.

12. The isolated fusion protein of claim 11 , wherein the cleavage sequence is susceptible to cleavage by a protease selected from FXIa, FXIIa, kallikrein, FVIIa, FIXa, FXa, thrombin, elastase-2, granzyme B, MMP-12, MMP-13, MMP-17 or MMP-20, TEV, enterokinase, rhinovirus 3C protease, and sortase A.

13. A pharmaceutical composition comprising the fusion protein of claim 8 and a pharmaceutically acceptable carrier.

14. A nucleic acid comprising a polynucleotide sequence selected from

(a) a polynucleotide encoding the isolated fusion protein of claim 8 ; or

(b) the complement of the polynucleotide of (a).

15. An expression vector comprising the polynucleotide sequence of claim 14 .

16. The expression vector of claim 15 , further comprising a recombinant regulatory sequence operably linked to the polynucleotide sequence.

17. A host cell, comprising the expression vector of claim 16 .

18. The host cell of claim 17 , wherein the host cell is E. coli.

19. The host cell of claim 17 , wherein the host cell is a Chinese hamster ovary (CHO) cell.

Assignments (5)
CONFIRMATORY LICENSE Recorded Oct 12, 2022
From: AMUNIX PHARMACEUTICALS INC
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 061646/0358 →
CHANGE OF NAME Recorded Feb 4, 2021
From: AMUNIX OPERATING INC.
To: AMUNIX PHARMACEUTICALS, INC.
Reel/Frame 055223/0978 →
CHANGE OF NAME Recorded Apr 18, 2019
From: AMUNIX OPERATING INC.
To: AMUNIX PHARMACEUTICALS, INC.
Reel/Frame 048943/0733 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 21, 2018
From: SCHELLENBERGER, VOLKER; SILVERMAN, JOSHUA; WANG, CHIA-WEI; SPINK, BENJAMIN; STEMMER, WILLEM P.; GEETHING, NATHAN; TO, WAYNE; CLELAND, JEFFREY L.
To: AMUNIX, INC.
Reel/Frame 045302/0241 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 21, 2018
From: AMUNIX, INC.
To: AMUNIX OPERATING INC.
Reel/Frame 045302/0392 →
Continuity (14)
Continuation 15154223 · May 13, 2016
Continuation 14168973 · Jan 30, 2014
Continuation 12699761 · Feb 3, 2010
Provisional Application 61281109 · Nov 12, 2009
Provisional Application 61280955 · Nov 10, 2009
Provisional Application 61280956 · Nov 10, 2009
Provisional Application 61245490 · Sep 24, 2009
Provisional Application 61243707 · Sep 18, 2009
Provisional Application 61236836 · Aug 25, 2009
Provisional Application 61236493 · Aug 24, 2009
Provisional Application 61268193 · Jun 8, 2009
Provisional Application 61185112 · Jun 8, 2009
Provisional Application 61149669 · Feb 3, 2009
Related Publication 20180244736A1 · Aug 30, 2018