US2012058136A1PendingUtilityA1
NON-SPLICING VARIANTS OF gp350/220
Est. expiryApr 18, 2014(expired)· nominal 20-yr term from priority
A61K 39/245A61P 31/12C07K 14/005A61K 38/00C12N 7/00A61K 39/12A61P 31/22A61K 2039/55566A61P 37/04A61K 2039/5555C12N 2710/16222C12N 2710/16234
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Claims
Abstract
Compositions comprising gp350 variant DNA and amino acid sequences are provided, as are vectors and host cells containing such sequences. Also provided is a process for producing homogeneous gp350 protein recombinantly and in the absence of production of gp220 protein, pharmaceutical compositions containing such protein and prophylactic treatments making use of such proteins.
Claims
exact text as granted — not AI-modified1 . An isolated DNA sequence that codes on expression for an homogeneous gp350 protein.
2 . A DNA sequence of claim 1 further characterized by having a nucleotide sequence in which at least one native nucleotide encoding serine at position 501 of FIG. 1 is replaced with a non-native nucleotide and in which at least one native nucleotide encoding glycine at position 698 is replaced with a non-native nucleotide.
3 . A DNA sequence of claim 1 wherein said homogeneous gp350 protein is further characterized by encoding an amino acid sequence having a deletion of at least 8 amino acids in the transmembrane region.
4 . A DNA sequence of claim 3 wherein said homogeneous gp350 protein is further characterized by encoding an amino acid sequence selected from the group consisting of
(a) amino acid 19 through amino acid 862 of FIG. 1 .
(b) amino acid 1 through amino acid 862 of FIG. 1 .
(c) amino acid 19 through amino acid 862 and amino acid 882 through amino acid 907 of FIG. 1 .
(d) amino acid 1 through amino acid 862 and amino acid 882 through amino acid 907 of FIG. 1 .
5 . A vector comprising a DNA sequence of claim 1 .
6 . A host cell transformed with a DNA sequence of claim 1 in operative association with an expression control sequence capable of directing replicated and expression of said DNA sequence.
7 . A process for producing a homogenous gp350 protein comprising culturing a host cell of claim 6 in a suitable culture medium and isolating said homogeneous gp350 protein from said cell.
8 . A homogeneous gp350 protein, made according to the process of claim 7 .
9 . A homogeneous gp350 protein, wherein one or more of the native nucleotides encoding the donor splice site and acceptor splice site are replaced with substitute nucleotide(s) different from said native nucleotide(s) which preserve the amino acid sequence of said donor and acceptor sites.
10 . A pharmaceutical composition comprising the homogeneous gp350 protein of claim 8 in admixture with a pharmaceutically acceptable carrier.
11 . A method of prophylactic treatment of a EBV-related disease or condition comprising administering to a patient a pharmaceutical composition of claim 10 in an amount sufficient to stimulate an immune response in said patient.
12 . A pharmaceutical composition comprising the homogeneous gp350 protein of claim 9 in admixture with a pharmaceutically acceptable carrier.
13 . A method of prophylactic treatment of a EBV-related disease or condition comprising administering to a patient a pharmaceutical composition of claim 12 in an amount sufficient to stimulate an immune response in said patient.Join the waitlist — get patent alerts
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