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用于癌症检测与治疗的工程化抗体Fv片段:二硫键稳定的Fv片段

Engineering antibody Fv fragments for cancer detection and therapy: disulfide-stabilized Fv fragments.

作者信息

Reiter Y, Brinkmann U, Lee B, Pastan I

机构信息

Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-4255, USA.

出版信息

Nat Biotechnol. 1996 Oct;14(10):1239-45. doi: 10.1038/nbt1096-1239.

Abstract

Disulfide-stabilized Fv fragments of antibodies (dsFv) are molecules in which the VH-VL heterodimer is stabilized by an interchain disulfide bond engineered between structurally conserved framework positions distant from complementarity-determining regions (CDRs). This method of stabilization is applicable for the stabilization of many antibody Fvs and has also been applied to a T-cell receptor Fv. A summary of the design strategy, and the construction and production of various dsFvs and dsFv-fusion proteins is presented. Included in the discussion are the biochemical features of dsFvs in comparison with scFvs, the effect of disulfide stabilization on Fv binding and activity, and various applications of dsFvs and dsFv-immunotoxins for tumor imaging and the treatment of solid tumors in animal models.

摘要

抗体的二硫键稳定化Fv片段(dsFv)是这样一种分子,其中VH-VL异二聚体通过在远离互补决定区(CDR)的结构保守框架位置之间设计的链间二硫键得以稳定。这种稳定化方法适用于许多抗体Fv的稳定化,并且也已应用于T细胞受体Fv。本文介绍了设计策略以及各种dsFv和dsFv融合蛋白的构建与生产。讨论内容包括dsFv与单链Fv(scFv)相比的生化特性、二硫键稳定化对Fv结合和活性的影响,以及dsFv和dsFv免疫毒素在动物模型中用于肿瘤成像和实体瘤治疗的各种应用。

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