IP Library Granted Patent US 9,340,813
Granted Patent B2
US 9,340,813 · App. 14/038,328 · Granted May 17, 2016

Methods of intracellular conversion of single-chain proteins into their di-chain form

Inventors: Sanjiv Ghanshani (Irvine, CA); Linh Q. Le (Tustin, CA); Yi Liu (Irvine, CA); Lance E. Steward (Irvine, CA)
Assignee: Allergan, Inc.
C12P21/00C07K14/33C12N9/506C12N15/70C07K2319/50C12N2799/026
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Quick Facts
Patent No.
US 9,340,813
App. No.
14/038,328
Granted
May 17, 2016
Kind
B2
Abstract

The present specification discloses expression constructs comprising single-chain proteins comprising a di-chain loop region comprising an exogenous protease cleavage site and a protease that can cleave the exogenous protease cleavage site located within the di-chain loop, cell compositions comprising such expression construct, and intracellular methods of converting the single-chain protein into its di-chain form.

Claims (8)

1. An intracellular method of converting a single-chain protein into its di-chain form, the method comprising the steps of:

(a) growing a cell comprising a dual expression construct at a first temperature for a certain period of time in order to achieve maximal cell density, the dual expression construct comprising:

(i) an open reading frame encoding the single-chain protein comprising a di-chain loop region comprising an exogenous protease cleavage site; and

(ii) an open reading frame encoding a protease; wherein the protease can cleave the exogenous protease cleavage site located within the di-chain loop;

(b) growing the cell at a second temperature for a certain period of time in order to achieve maximal induction of protein expression from the open reading frame encoding the single-chain protein,

wherein growth at step (b) induces expression of the single-chain protein and the protease from the dual expression construct; and

wherein the produced protease cleaves the single-chain protein at the exogenous protease cleavage site located within the di-chain loop region, thereby converting the single-chain protein into its di-chain form.

2. The method according to claim 1 , wherein the exogenous protease cleavage site is an enterokinase protease cleavage site, a human rhinovirus 3C protease cleavage site, a human enterovirus 3C protease cleavage site, a Tobacco Vein Mottling Virus (TVMV) protease cleavage site, a subtilisin protease cleavage site, or a Caspase 3 protease cleavage site.

Continuity (3)
Continuation 13575222
Provisional Application 61286963 · Jan 25, 2010
Related Publication 20140030759A1 · Jan 30, 2014