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针对Etk激酶的人源单域中和细胞内抗体:一种抑制细胞转化的新方法。

Human single-domain neutralizing intrabodies directed against Etk kinase: a novel approach to impair cellular transformation.

作者信息

Paz Keren, Brennan Laura A, Iacolina Michelle, Doody Jacqueline, Hadari Yaron R, Zhu Zhenping

机构信息

Department of Antibody Technology and Protein Sciences, ImClone Systems, 180 Varick Street, New York, New York 10014, USA.

出版信息

Mol Cancer Ther. 2005 Nov;4(11):1801-9. doi: 10.1158/1535-7163.MCT-05-0174.

Abstract

Etk, the 70-kDa member of the Tec family of nonreceptor protein tyrosine kinases, is expressed in a variety of hematopoietic, epithelial, and endothelial cells and was shown to be involved in several cellular processes, including proliferation, differentiation, and motility. In this study, we describe a novel approach using a human single-domain antibody phage display library for the generation of intrabodies directed against Etk. These single-domain antibodies bind specifically to recombinant Etk and efficiently block its kinase activity. When expressed in transformed cells, these antibodies associated tightly with Etk, leading to significant blockade of Etk enzymatic activity and inhibition of clonogenic cell growth in soft agar. Our results indicate that Etk may play a role in Src-induced cellular transformation and thus may represent a good target for cancer intervention. Furthermore, our single-domain antibody-based intrabody system proves to be an excellent tool for future intracellular targeting of other signaling molecules.

摘要

Etk是Tec家族非受体蛋白酪氨酸激酶中的70 kDa成员,在多种造血细胞、上皮细胞和内皮细胞中表达,并被证明参与多种细胞过程,包括增殖、分化和迁移。在本研究中,我们描述了一种使用人单域抗体噬菌体展示文库生成针对Etk的胞内抗体的新方法。这些单域抗体特异性结合重组Etk并有效阻断其激酶活性。当在转化细胞中表达时,这些抗体与Etk紧密结合,导致Etk酶活性显著阻断,并抑制软琼脂中的克隆细胞生长。我们的结果表明,Etk可能在Src诱导的细胞转化中起作用,因此可能是癌症干预的良好靶点。此外,我们基于单域抗体的胞内抗体系统被证明是未来对其他信号分子进行细胞内靶向的优秀工具。

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