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EP0136694A2 Expired / Lapsed EP ⏱️ 0.0 years remaining

Production of monomeric human gamma-interferon

Assignee: Takeda Pharmaceutical Co Ltd
•
Filing: 1984-10-02
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Granted: —
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Expires: 2004-10-02
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Abstract

Abstract Monomeric human -y-interferon is efficiently produced by subjecting crude human γ-interferon to gel filtration under the coexistence of a reducing sulfur compound and a protein-denaturing agent.

Inventors

  • 👤 Kiyoshi Nara
  • 👤 Susumu Honda

Bibliographic Details

Application Number —
Jurisdiction EP
Data Source google_patents
Last Synchronized 2026-10-24 22:59
CPC Classifications
C; C12; C12N; C12N15/00; C07; C07K; C07K1/00; C07K1/107; C07K1/113; C07K1/1133; A; A61; A61P; A61P43/00; C07K14/00; C07K14/435; C07K14/52; C07K14/555; C07K14/57; C12N15/09; C12N15/63; C12N15/70; C12N15/71; Y; Y10; Y10S; Y10S435/00; Y10S435/811; Y10S930/00; Y10S930/01; Y10S930/14; Y10S930/142

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 28 words
A method for producing monomeric human y-interferon, which comprises subjecting crude human y-interferon to gel filtration under the coexistence of a reducing sulfur compound and a protein-denaturing agent.
Claim 2
Independent Claim 28 words
A method for producing monomeric human y-interferon, which comprises subjecting crude human y-interferon to gel filtration under the coexistence of a reducing sulfur compound and a protein-denaturing agent.
Claim 3
Dependent Claim 16 words
A method according to Claim 1, wherein the reducing sulfur compound is an organic sulfur compound.
Claim 4
Dependent Claim 39 words
A method according to Claim 2, wherein the organic sulfur compound is a member selected from a group consisting of cysteine, N-acetylcysteine, N-acetylhomocysteine, glutathione (reduced form), thioethanolamine, monothioglycerol, dithiothreitol, thioalkane having 1-7 carbon atoms and formaldehyde sodium sulfoxilate dihydrate.
Claim 5
Dependent Claim 15 words
A method according to Claim 3, wherein the organic sulfur compound is glutathione (reduced form).
Claim 6
Dependent Claim 24 words
A method according to Claim 1, wherein the protein-denaturing agent is a member selected from a group consisting of guanidine salt, urea and thiocyanate.
Claim 7
Dependent Claim 13 words
A method according to Claim 5, wherein the protein-denaturing agent is guanidine salt.
Claim 8
Dependent Claim 15 words
A method according to Claim 1, wherein the human y-interferon is a recombinant human y-interferon.
Claim 9
Dependent Claim 25 words
A method according to Claim 1, wherein the crude human y-interferon is an eluate of an antibody column loaded by an extract containing human y-interferon.
Claim 10
Dependent Claim 22 words
A method according to Claim 1, wherein the gel is a member selected from a group consisting of dextran, polyacrylamide and agarose.
Claim 11
Dependent Claim 12 words
A method according to Claim 9, wherein the gel is a dextran.
Claim 12
Dependent Claim 48 words
A method according to Claim 1, wherein the gel filtration is conducted by loading crude human y-interferon dissolved in a buffer solution containing a reducing sulfur compound and a protein-denaturing agent on a column packed with granular gel and then eluting the y-interferon by the same buffer solution.
Claim 13
Dependent Claim 33 words
A method according to Claim 11, wherein the buffer solution contains the reducing sulfur compound and the protein-denaturing agent in a concentration of 1 to 100 mM and 0.1 to 7 M, respectively.
Claim 14
Dependent Claim 16 words
A method according to Claim 11, wherein the buffer solution is of pH 5.0 to 8.0.
Claim 15
Dependent Claim 19 words
A method according to Claim 11, wherein the elution is conducted at a space velocity of 0.1 to 10.
Claim 16
Dependent Claim 42 words
A method according to Claim 1, wherein the resulting monomeric human y-interferon solution is further subjected to gel filtration using a gel suited for removing low molecular weight compounds to obtain monomeric human y-interferon free from reducing sulfur compound and protein-denaturing agent.

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