IP Library Granted Patent US 10,973,888
Granted Patent B2
US 10,973,888 · App. 16/985,742 · Granted Apr 13, 2021

Human alpha-galactosidase variants

Inventors: Nicholas J. Agard (San Francisco, CA); Mathew G. Miller (San Carlos, CA); Xiyun Zhang (Fremont, CA); Gjalt W. Huisman (Redwood City, CA)
Assignee: Codexis, Inc.
A61K38/47A61K9/0019C12N9/2465C12Y302/01022
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Quick Facts
Patent No.
US 10,973,888
App. No.
16/985,742
Granted
Apr 13, 2021
Kind
B2
Abstract

The present invention provides engineered human alpha-galactosidase polypeptides and compositions thereof. The engineered human alpha-galactosidase polypeptides have been optimized to provide improved stability under both acidic (pH<4.5) and basic (pH>7) conditions. The invention also relates to the use of the compositions comprising the engineered human alpha-galactosidase polypeptides for therapeutic purposes.

Claims (13)

1. A recombinant alpha galactosidase A comprising an amino acid sequence comprising at least 95%, sequence identity to SEQ ID NO: 5, wherein said amino acid sequence comprises a mutation at positions 44 and 206, wherein said positions are numbered with reference to SEQ ID NO: 5.

2. The recombinant alpha galactosidase A of claim 1 , wherein said recombinant alpha galactosidase A is a recombinant human alpha galactosidase A.

3. The recombinant alpha galactosidase A of claim 1 , wherein said recombinant alpha galactosidase A exhibits at least one improved property selected from: i) increased thermostability; ii) enhanced catalytic activity; iii) increased tolerance to pH 7.4; iv) increased tolerance to pH 4.3; v) increased tolerance to serum; or vi) reduced immunogenicity; or a combination of any of i), ii), iii), iv), v), or vi), as compared to a reference alpha galactosidase A.

4. The recombinant alpha galactosidase A of claim 3 , wherein said recombinant alpha galactosidase A is more thermostable than the alpha galactosidase A of SEQ ID NO:5.

5. The recombinant alpha galactosidase A of claim 3 , wherein said recombinant alpha galactosidase A is more stable at pH 7.4 than the alpha galactosidase A of SEQ ID NO:5.

6. The recombinant alpha galactosidase A of claim 3 , wherein said recombinant alpha galactosidase A is more stable at pH 4.3 than the alpha galactosidase A of SEQ ID NO:5.

7. The recombinant alpha galactosidase A of claim 3 , wherein said recombinant alpha galactosidase A is more stable to exposure to serum than the alpha galactosidase A of SEQ ID NO:5.

8. The recombinant alpha galactosidase A of claim 3 , wherein said recombinant alpha galactosidase A is less immunogenic than wild-type alpha galactosidase A.

9. The recombinant alpha galactosidase A of claim 1 , wherein the amino acid sequence of said recombinant alpha galactosidase further comprises at least one mutation at a position selected from position 2, 7, 8, 10, 14, 15, 17, 20, 21, 23, 24, 30, 31, 34, 36, 37, 39, 40, 41, 43, 47, 48, 52, 53, 56, 59, 64, 65, 66, 67, 74, 76, 77, 80, 84, 87, 88, 91, 92, 93, 94, 95, 96, 100, 102, 105, 113, 120, 123, 124, 125, 130, 133, 136, 143, 144, 147, 155, 156, 158, 159, 160, 161, 162, 163, 165, 166, 167, 168, 169, 170, 174, 177, 178, 179, 180, 181, 182, 186, 187, 189, 190, 195, 198, 199, 208, 210, 217, 219, 221, 228, 230, 234, 237, 238, 246, 247, 249, 252, 253, 254, 255, 256, 257, 258, 259, 261, 262, 263, 266, 269, 270, 271, 273, 274, 276, 277, 281, 283, 284, 287, 290, 293, 295, 299, 301, 302, 303, 305, 308, 314, 316, 317, 319, 322, 325, 326, 337, 339, 343, 344, 345, 346, 348, 349, 350, 352, 353, 354, 359, 362, 365, 367, 368, 369, 371, 373, 374, 375, 376, 377, 384, 385, 386, 387, 388, 389, 390, 391, 392, 393, 394, 395, 396, 397, and 398, wherein the positions are numbered relative to the amino acid sequence set forth in SEQ ID NO: 5.

10. The recombinant alpha galactosidase A of claim 1 , wherein said recombinant alpha galactosidase A is purified.

11. A composition comprising said recombinant alpha galactosidase A of claim 1 .

12. A pharmaceutical composition for the treatment of Fabry disease, comprising the enzyme composition of claim 11 , further comprising a pharmaceutically acceptable carrier and/or excipient.

13. The pharmaceutical composition of claim 12 , wherein said composition is suitable for parenteral injection or infusion to a human.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Aug 21, 2024
From: INNOVATUS LIFE SCIENCES LENDING FUND I, LP, AS COLLATERAL AGENT
To: CODEXIS, INC.
Reel/Frame 068361/0757 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2024
From: CODEXIS, INC.
To: CROSSWALK THERAPEUTICS, INC.
Reel/Frame 068660/0439 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2024
From: AGARD, NICHOLAS J.; MILLER, MATHEW G.; ZHANG, XIYUN; HUISMAN, GJALT W.
To: CODEXIS, INC.
Reel/Frame 068164/0481 →
SECURITY INTEREST Recorded Feb 15, 2024
From: CODEXIS, INC.
To: INNOVATUS LIFE SCIENCES LENDING FUND I, LP, AS COLLATERAL AGENT
Reel/Frame 066600/0650 →
Continuity (4)
Continuation 15529383
Provisional Application 62095313 · Dec 22, 2014
Provisional Application 62216452 · Sep 10, 2015
Related Publication 20200360489A1 · Nov 19, 2020
Cited By (3)
US 12,257,291 US 12,263,207 US 12,286,655