Enzymes and methods for cleaving n-glycans from glycoproteins

US2016287680A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016287680-A1
Application numberUS-201615079949-A
CountryUS
Kind codeA1
Filing dateMar 24, 2016
Priority dateFeb 14, 2012
Publication dateOct 6, 2016
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

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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.

First claim

Opening claim text (preview).

What is claimed is: 1 . A method of increasing the efficiency of protein digestion in an individual, comprising administering a pharmaceutical composition comprising a recombinant polypeptide comprising a sequence at least 90% identical to SEQ ID NO:4, wherein the polypeptide can cleave high mannose, complex, and hybrid N-glycans from a glycoprotein, and wherein the polypeptide lacks a transmembrane domain to the individual, thereby increasing the efficiency of protein digestion in the individual. 2 . The method of claim 2 , wherein the individual is an infant. 3 . A method of inducing satiety in an individual, comprising administering a pharmaceutical composition comprising a recombinant polypeptide comprising a sequence at least 90% identical to SEQ ID NO:4, wherein the polypeptide can cleave high mannose, complex, and hybrid N-glycans from a glycoprotein, and wherein the polypeptide lacks a transmembrane domain to the individual, thereby inducing satiety in the individual. 4 . 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. 5 . The method of claim 4 , wherein the glycoprotein comprises a high mannose N-glycan. 6 . The method of claim 4 , wherein the glycoprotein comprises a complex N-glycan. 7 . The method of claim 4 , wherein the glycoprotein comprises a hybrid N-glycan. 8 . A method of recombinantly producing a polypeptide, wherein said polypeptide comprises 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, the method comprising culturing a cell comprising a recombinant polynucleotide encoding the polypeptide under conditions appropriate for expression of the polypeptide, and contacting the polypeptide with a glycoprotein comprising a high mannose, complex, or hybrid N-glycan, thereby deglycosylating the glycoprotein, thereby recombinantly producing the polypeptide. 9 . The method of claim 8 , wherein the polypeptide lacks a transmembrane domain that spans a cell membrane. 10 . The method of claim 8 , further comprising isolating the polypeptide. 11 . The method of claim 8 , wherein the glycoprotein is selected from the group consisting of: lactoferrin, whey, and immunoglobulin. 12 . 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. 13 . The composition of claim 12 , wherein the glycoprotein is selected from the group consisting of: lactoferrin, whey, and immunoglobulin. 14 . The composition of claim 12 , wherein the N-glycan comprises core fucosylation, terminal fucosylation, or terminal sialylation. 15 . The composition of claim 12 , wherein the polypeptide is a transmembrane protein in a cell membrane protein in a cell. 16 . The composition of claim 12 , wherein the glycoprotein comprises a high mannose N-glycan. 17 . The composition of claim 12 , wherein the glycoprotein comprises a complex N-glycan. 18 . The composition of claim 12 , wherein the glycoprotein comprises a hybrid N-glycan.

Assignees

Inventors

Classifications

  • Drugs for immunological or allergic disorders · CPC title

  • Other enzymes · CPC title

  • Proteins from microorganisms · CPC title

  • Glycopeptides, glycoproteins · CPC title

  • hydrolysing N- glycosyl compounds (3.2.2) · CPC title

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What does patent US2016287680A1 cover?
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 descr…
Who is the assignee on this patent?
Univ California
What technology area does this patent fall under?
Primary CPC classification A61K38/47. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Oct 06 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).