ENGINEERING DISULFIDE-LINKED SINGLE-CHAIN FV DIMERS [(SFV')(2)] WITH IMPROVED SOLUTION AND TARGETING PROPERTIES - ANTIDIGOXIN-26-10 (SFV')(2) AND ANTI-C-ERBB-2 741F8 (SFV')(2) MADE BY PROTEIN-FOLDING AND BONDED THROUGH C-TERMINAL CYSTEINYL PEPTIDES

被引:45
作者
MCCARTNEY, JE
TAI, MS
HUDZIAK, RM
ADAMS, GP
WEINER, LM
JIN, D
STAFFORD, WF
LIU, S
BOOKMAN, MA
LAMINET, AA
FAND, I
HOUSTON, LL
OPPERMANN, H
HUSTON, JS
机构
[1] CREAT BIOMOLECULES INC, HOPKINTON, MA 01748 USA
[2] FOX CHASE CANC CTR, DEPT MED ONCOL, PHILADELPHIA, PA 19111 USA
[3] BOSTON BIOMED RES INST, BOSTON, MA 02114 USA
[4] CETUS ONCOL CORP, EMERYVILLE, CA 94608 USA
[5] CTR MOLEC MED & IMMUNOL, GARDEN STATE CANC CTR, NEWARK, NJ 07103 USA
来源
PROTEIN ENGINEERING | 1995年 / 8卷 / 03期
关键词
C-ERB-2 EXTRACELLULAR DOMAIN; DIGOXIN; IMMUNO-TARGETING; (SFV')(2) DIMERS; SINGLE-CHAIN FV;
D O I
10.1093/protein/8.3.301
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Single-chain Fv fusions with C-terminal cysteinyl peptides (sFv') have been engineered using model sFv proteins based upon the 26-10 anti-digoxin IgG and 741F8 anti-c-erbB-2 IgG monoclonal antibodies, As part of the 741F8 sFv construction process, the PCR-amplified 741F8 V-H gene was modified in an effort to correct possible primer-induced errors, Genetic replacement of the N-terminal beta-strand sequence of 741F8 V-H With that from the FR1 of anti-c-erbB-2 520C9 V-H resulted in a dramatic improvement of sFv folding yields, Folding in urea-glutathione redox buffers produced active sFv' with a protected C-terminal sulfhydryl, presumably as the mixed disulfide with glutathione, Disulfide-bonded (sFv')(2) homodimers were made by disulfide interchange or oxidation after reductive elimination of the blocking group, Both 26-10 (sFv')(2) and 741F8 (sFv')(2) existed as stable dimers that were well behaved in solution, whereas 741F8 sFv and sFv' exhibited considerable self-association. The 741F8 sFv binds to the extracellular domain (ECD) of the c-erbB-2 oncogene protein, which is often overexpressed in breast cancer and other adenocarcinomas. The recombinant ECD was prepared to facilitate the analysis of 741F8 binding site properties; the cloned ECD gene, modified to encode a C-terminal Ser-Gly-His(6) peptide, was transfected into Chinese hamster ovary cells using a vector that also expressed dihydrofolate reductase to facilitate methotrexate amplification, Optimized cell lines expressed ECD-His(6) at high levels in a cell bioreactor; after isolation by immobilized metal affinity chromatography, final ECD yields were as high as 47 mg/l, An animal tumor model complemented physicochemical studies of 741F8 species and indicated increased tumor localization of the targeted 741F8 (sFv')(2) over other monovalent 741F8 species.
引用
收藏
页码:301 / 314
页数:14
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