U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Process for controlling intracellular glycosylation of proteins

Patent 5047335 Issued on September 10, 1991. Estimated Expiration Date: Icon_subject December 21, 2008. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Gene amplification in eukaryotic cells
Patent #: 4656134
Issued on: 04/07/1987
Inventor: Ringold

cDNA clones coding for polypeptides exhibiting multi-lineage cellular growth factor activity
Patent #: 4695542
Issued on: 09/22/1987
Inventor: Yokota ,   et al.

Vectors and methods for transformation of eucaryotic cells
Patent #: 4740461
Issued on: 04/26/1988
Inventor: Kaufman

Process for producing human epidermal growth factor and analogs thereof
Patent #: 4743679
Issued on: 05/10/1988
Inventor: Cohen ,   et al.

CDNA clones coding for polypeptides exhibiting IGE binding factor activity
Patent #: 4758511
Issued on: 07/19/1988
Inventor: Martens ,   et al.

High yield production of active Factor IX
Patent #: 4770999
Issued on: 09/13/1988
Inventor: Kaufman ,   et al.

Vectors and compounds for expression of human protein C Patent #: 4775624
Issued on: 10/04/1988
Inventor: Bang ,   et al.

Inventors

Assignee

Application

No. 288618 filed on 12/21/1988

US Classes:

435/69.1, Recombinant DNA technique included in method of making a protein or polypeptide435/320.1, VECTOR, PER SE (E.G., PLASMID, HYBRID PLASMID, COSMID, VIRAL VECTOR, BACTERIOPHAGE VECTOR, ETC.) BACTERIOPHAGE VECTOR, ETC.)435/466, The polynucleotide is a shuttle vector or a transiently replicating hybrid vector536/23.2, Encodes an enzyme536/24.1Non-coding sequences which control transcription or translation processes (e.g., promoters, operators, enhancers, ribosome binding sites, etc.)

Examiners

Primary: Schwartz, Richard A.
Assistant: Nolan, S. L.

Attorney, Agent or Firm

International Classes

C12N 015/00
C12N 015/56
C12N 015/79

Abstract

A process for controlling the glycosylation of protein in a cell wherein the cell is genetically engineered to produce one or more enzymes which provide internal control of the cell's glycosylation mechanism. A Chinese hamster ovary (CHO) cell line is genetically engineered to produce a sialyltransferase. This supplemental sialyltransferase modifies the CHO glycosylation machinery to produce glycoproteins having carbohydrate structures which more closely resemble naturally occurring human glycoproteins.

Other References

  • Narimatsu et al, 1986, Proc. Natl. Acad. Sci. U.S.A., vol. 83, pp. 4720-4724
  • Kadam et al, 1985, Journal of Bacteriology, vol. 161, pp. 277-284
  • J. Weinstein, et al., Primary Structure of ଲ-Galactoside 댒,6-Sialyltransferase, Journal of Biological Chemistry, pp. 17735-17743, Dec. 25, 1987
  • J. Weinstein, et al., Sialylation of Glycoprotein Oligosaccharides N-Linked to Asparagine, Journal of Biological Chemistry, Nov. 25, 1982, pp. 13845-13853
  • M. Takeuchi et al., Comparative Study of the Asparagine-Linked Sugar Chains of Human Erythropoietins Purified From Urine and the Culture Medium of Recombinant Chinese Hamster Ovary Cells, Jour. of Bio. Chem., Mar. 15, 1988, pp. 3657-366
PatentsPlus Images
Enhanced PDF formats
loading...
PatentsPlus: add to cart
PatentsPlus: add to cartSearch-enhanced full patent PDF image
$9.95more info
 
Sign InRegister
Username  
Password   
forgot password?