IP Library Granted Patent US 10,071,142
Granted Patent B2
US 10,071,142 · App. 15/079,949 · Granted Sep 11, 2018

Enzymes and methods for cleaving N-glycans from glycoproteins

Inventors: Daniel Garrido (Santiago, CL); J. Bruce German (Davis, CA); Carlito B. Lebrilla (Davis, CA); David A. Mills (Oakland, CA)
Assignee: The Regents of the University of California
A61K38/47A23C9/1216A23L2/52A23L33/195A61K31/715A61K35/741A61K38/40C07K14/79C12N9/2402C12N9/2497C12P19/04C12P21/005A61K38/00C12Y302/01096Y02P20/52
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Quick Facts
Patent No.
US 10,071,142
App. No.
15/079,949
Granted
Sep 11, 2018
Kind
B2
Abstract

Provided herein are deglycosylating enzymes that remove a broad range of N-glycans from N-glycosylated proteins. Further provided are methods of recombinantly producing and expressing the deglycosylating enzymes. The presently described deglycosylating enzymes can be used to produce free glycans for characterization, and for prebiotic and immunostimulatory uses. In addition, the presently described deglycosylating enzymes can be used to produce deglycosylated proteins for characterization, to improve digestion, and to reduce immunogenicity.

Claims (14)

1. A method of deglycosylating a glycoprotein comprising a high mannose, complex, or hybrid N-glycan, the method comprising

contacting the glycoprotein with a polypeptide comprising a sequence at least 90% identical to SEQ ID NO:4, wherein the polypeptide lacks a transmembrane domain, thereby deglycosylating the glycoprotein and generating deglycosylated protein and free glycans.

2. The method of claim 1 , wherein the glycoprotein comprises a high mannose N-glycan.

3. The method of claim 1 , wherein the glycoprotein comprises a complex N-glycan.

4. The method of claim 1 , wherein the glycoprotein comprises a hybrid N-glycan.

5. A composition comprising:

(i) a recombinant polypeptide comprising a sequence at least 90% identical to SEQ ID NO:4 wherein said polypeptide can cleave high mannose, complex, and hybrid N-glycans from a glycoprotein and wherein the polypeptide lacks a transmembrane domain; and

(ii) a glycoprotein, wherein the glycoprotein comprises a high mannose, complex, or hybrid N-glycan.

6. The composition of claim 5 , wherein the glycoprotein is selected from the group consisting of: lactoferrin, whey, and immunoglobulin.

7. The composition of claim 5 , wherein the N-glycan comprises core fucosylation, terminal fucosylation, or terminal sialylation.

8. The composition of claim 5 , wherein the polypeptide is a transmembrane protein in a cell membrane protein in a cell.

9. The composition of claim 5 , wherein the glycoprotein comprises a high mannose N-glycan.

10. The composition of claim 5 , wherein the glycoprotein comprises a complex N-glycan.

11. The composition of claim 5 , wherein the glycoprotein comprises a hybrid N-glycan.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 31, 2016
From: GARRIDO, DANIEL; GERMAN, J. BRUCE; LEBRILLA, CARLITO B.; MILLS, DAVID A
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 038749/0681 →
Continuity (3)
Continuation 14378190
Provisional Application 61598593 · Feb 14, 2012
Related Publication 20160287680A1 · Oct 6, 2016