发明名称 Modified peptide and the use thereof, DNA, expression vector, host cell, pharmaceutical composition, and a method of preparing the pharmacologically active compound
摘要 <p>The present invention relates to a modified peptide of the general formula (X1)a-F1-(X2)b, and multimers thereof, wherein F1 is an Fc domain; X1 and X2 are each independently selected from -(L1)c-P1, -(L1)c-P1-(L2)d-P2, -(L1)c-P1-(L2)d-P2-(L3)e-P3, and -(L1)c-P1-(L2)d-P2-(L3)e-P3-(L4)f-P4 wherein P1, P2, P3 and P4 are each independently randomised sequences of pharmacologically active peptides; L1, L2, L3 and L4 are linkers; and a, b, c, d, e and f are 0 or 1, provided that at least one of a and b is 1, and wherein "peptide" refers to molecules of 2 to 40 amino acids and wherein neither X1 nor X2 is a native protein. The invention further relates to use of that product, a DNA encoding thereof, an expression vector containing the DNA, and a host cell containing the vector. The invention further relates to pharmaceutical composition containing that product. The pharmacologically active compounds are prepared by a process comprising: a) selecting a peptide that modulates the activity of a protein of interest; and b) preparing a compound comprising at least one Fc domain covalently linked to at least one amino acid of the selected peptide.</p>
申请公布号 SK287037(B6) 申请公布日期 2009.10.07
申请号 SK20010000525 申请日期 1999.10.25
申请人 AMGEN INC. 发明人 FEIGE ULRICH;LIU CHUAN-FA;CHEETHAM JANET;BOONE THOMAS CHARLES
分类号 G01N33/50;A61K38/00;A61P3/04;A61P19/02;A61P29/00;A61P31/04;A61P31/12;A61P31/18;A61P35/00;A61P35/02;A61P37/02;A61P43/00;C07K;C07K14/47;C07K14/505;C07K14/52;C07K14/525;C07K14/545;C07K16/18;C07K19/00;C12N;C12N1/21;C12N9/64;C12N15/09;C12N15/62;C12N15/70;C12P21/02;C12R1/19;G01N33/15;G01N33/566 主分类号 G01N33/50
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