US2010260706A1PendingUtilityA1

Compositions and methods for improving production of recombinant polypeptides

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Assignee: BOGIN ORENPriority: Aug 15, 2007Filed: Dec 23, 2009Published: Oct 14, 2010
Est. expiryAug 15, 2027(~1.1 yrs left)· nominal 20-yr term from priority
A61P 5/00A61P 7/00A61P 9/10A61P 5/24A61P 9/00A61P 37/08A61P 35/02A61P 7/02A61P 7/06A61P 9/12A61P 43/00A61P 3/10A61P 31/12A61P 25/14A61P 3/04A61P 31/00A61P 27/06A61P 35/00A61P 25/28A61P 31/18A61P 31/04A61P 29/00A61P 25/04A61P 15/00C07K 14/00C07K 14/61C07K 2317/22C07K 14/535C07K 2317/622C07K 16/2863C07K 2319/33C07K 2317/626A61K 38/00C07K 16/32C07K 2317/569C07K 16/30A61P 1/16C07K 2319/00C07K 14/56A61P 13/12A61P 19/02A61P 17/02A61P 19/10C07K 16/40A61P 21/04A61P 11/00A61P 1/02A61P 1/04A61P 17/06C07K 2317/55A61P 15/10A61P 11/06
65
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Claims

Abstract

The present invention relates to biologically active polypeptides linked to one or more accessory polypeptides. The present invention also provides recombinant polypeptides including vectors encoding the subject proteinaceous entities, as well as host cells comprising the vectors. The subject compositions have a variety of utilities including a range of pharmaceutical applications.

Claims

exact text as granted — not AI-modified
1 - 148 . (canceled) 
     
     
         149 . A biologically active protein comprising at least two domains wherein (a) a first domain of said at least two domains comprises an amino acid sequence having and/or mediating said biological activity; and (b) a second domain of said at least two domains comprises an amino acid sequence consisting preferably of at least about 100 amino acid residues forming random coil conformation whereby said random coil conformation mediates an increased in vivo and/or in vitro stability of said biologically active protein. 
     
     
         150 . The biologically active protein according to  claim 149 , wherein said second domain forming random coil conformation consists of alanine, serine and proline residues. 
     
     
         151 . The biologically active protein according to  claim 149  or  150 , wherein said second domain forming random coil conformation comprises a plurality of amino acid repeats, wherein said repeat consist of Ala, Ser, and Pro residues and wherein no more than 6 consecutive amino acid residues are identical. 
     
     
         152 . The biologically active protein according to any one of  claims 149  to  151 , wherein said proline residues constitute more than 4% and less than 40% of the amino acids of said second domain forming random coil conformation. 
     
     
         153 . The biologically active protein according to any one of  claims 149  to  152 , wherein said second domain of said at least two domains comprises an amino acid sequence consisting of about 100 to 3000 amino acid residues forming random coil conformation. 
     
     
         154 . The biologically active protein according to any one of  claims 149  to  153 , wherein said polypeptide with biological activity is selected from the group consisting of binding molecules, antibody fragments, cytokines, growth factors, hormones or enzymes. 
     
     
         155 . The biologically active protein according to  claim 154  wherein said binding molecule is selected from the group consisting of antibodies, Fab fragments, F(ab′)2 fragments, CDR derived peptidomimetics, single chain variable fragments (scFv), domain antibodies and lipocalins. 
     
     
         156 . The biologically active protein according to any one of  claims 149  to  154 , wherein said polypeptide with biological activity is selected from the group consisting of granulocyte colony stimulating factor, human growth hormone, alphainterferon, betainterferon, gammainterferon, tumor necrosis factor, erythropoietin, coagulation factor VIII, gp120/gp160, soluble tumor necrosis factor I and II receptor, interleukin 2 and neutrophil gelatinase associated lipocalin. 
     
     
         157 . The biologically active protein according to any one of  claims 149  to  156 , wherein said increased in vivo stability of said biologically active protein is a prolonged plasma half life of said biologically active protein comprising said random coil forming second domain when compared to said biologically active protein lacking said random coil forming second domain. 
     
     
         158 . A composition comprising the biologically active protein according to any one of  claims 149  to  157 . 
     
     
         159 . The composition according to  claim 158 , which is a pharmaceutical composition, optionally further comprising a pharmaceutical acceptable carrier. 
     
     
         160 . A nucleic acid molecule encoding the biologically active protein of any one of  claims 149  to  157 . 
     
     
         161 . A vector comprising the nucleic acid of  claim 159 . 
     
     
         162 . A cell comprising the nucleic acid according to  claim 160  or the vector according to  claim 161 . 
     
     
         163 . A method for the preparing a biologically active protein comprising culturing the cell according to  claim 162  and isolating said biologically active protein from the culture. 
     
     
         164 . A method of treating a disease condition selected from the group consisting of hormone deficiency related disorders, autoimmune disease, cancer, anaemia, neovascular diseases, infectious/inflammatory diseases, thrombosis, myocardial infarction, diabetes, reperfusion injury, and a kidney disease, comprising administering to a subject in need thereof a composition according to  claim 159 .

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