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

机译:具有改进的解决方案和目标特性的工程二硫键单链FV测径仪[[SFV'](2)]-抗地高辛26-10(SFV')(2)和ANTI-C-ERBB-2 741F8(SFV' )(2)通过C末端半胱氨酸肽折叠并结合蛋白质制成

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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. [References: 67]
机译:已使用基于26-10抗地高辛IgG和741F8抗c-erbB-2 IgG单克隆抗体的sFv模型工程改造了具有C端半胱氨酰肽(sFv')的单链Fv融合蛋白,作为741F8的一部分在sFv的构建过程中,对PCR扩增的741F8 VH基因进行了修改,以纠正可能的引物诱导的错误,用抗c-erbB-FR1的FR1取代741F8 VH的N端β链序列。 2 520C9 VH极大地提高了sFv折叠率,在尿素-谷胱甘肽氧化还原缓冲液中折叠产生具有保护的C末端巯基的活性sFv',大概是二硫键与谷胱甘肽的二硫键结合(sFv')(2)还原性消除封闭基团后,通过二硫键交换或氧化制备同型二聚体,26-10(sFv')(2)和741F8(sFv')(2)均以稳定的二聚体存在,在溶液中表现良好,而741F8 sFv和sFv'表现出相当大的自我联想。 741F8 sFv与c-erbB-2癌基因蛋白的细胞外结构域(ECD)结合,而c-erbB-2癌基因蛋白通常在乳腺癌和其他腺癌中过表达。制备重组ECD以促进对741F8结合位点特性的分析。克隆的ECD基因经过修饰以编码C端Ser-Gly-His(6)肽,然后使用还表达二氢叶酸还原酶以促进甲氨蝶呤扩增的载体转染到中国仓鼠卵巢细胞中,优化的细胞系表达ECD-His( 6)在细胞生物反应器中含量高;通过固定金属亲和色谱分离后,最终ECD产量高达47 mg / l。动物肿瘤模型对741F8物种的物理化学研究进行了补充,并表明与其他单价741F8相比,靶向741F8(sFv')(2)的肿瘤定位增加了种类。 [参考:67]

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