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一种可用于阐明单克隆抗体-药物偶联物作用机制的双标记荧光技术的开发。

Development of a dual label fluorescence technique that can be utilized to elucidate the mechanism of action of monoclonal antibody-drug conjugates.

作者信息

Starling J J, Hinson N A, Marder P, Maciak R S, Laguzza B C, Corvalan J R, Smith W

机构信息

Lilly Research Laboratories, Indianapolis, Indiana 46285.

出版信息

Cancer Res. 1988 Nov 1;48(21):6211-6.

PMID:3048656
Abstract

A method is described that allows the simultaneous visualization and relative assessment of both the antibody and drug components of monoclonal antibody-drug conjugates at the target cell membrane. The antibody is detected by a fluorescein-conjugated anti-mouse immunoglobulin serum while the drug is visualized by rhodamine avidin or phycoerythrin-streptavidin binding to a biotinylated anti-Vinca alkaloid monoclonal antibody. This technique was effective in demonstrating the cell surface localization of a monoclonal antibody-Vinca alkaloid conjugate to human lung adenocarcinoma cells grown in vitro and was also used to demonstrate targeting of the conjugate in vivo to the membranes of these same tumor cells grown as a nude mouse xenograft. This method was also utilized to help elucidate the mechanism of action of monoclonal antibody-drug conjugates.

摘要

本文描述了一种方法,该方法能够同时在靶细胞膜上对单克隆抗体 - 药物偶联物的抗体和药物成分进行可视化及相对评估。通过荧光素偶联的抗小鼠免疫球蛋白血清检测抗体,而药物则通过罗丹明抗生物素蛋白或藻红蛋白 - 链霉抗生物素蛋白与生物素化的抗长春花生物碱单克隆抗体结合来可视化。该技术有效地证明了单克隆抗体 - 长春花生物碱偶联物在体外培养的人肺腺癌细胞上的细胞表面定位,并且还用于证明该偶联物在体内对作为裸鼠异种移植生长的相同肿瘤细胞膜的靶向作用。该方法还被用于帮助阐明单克隆抗体 - 药物偶联物的作用机制。

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