制备HIV单克隆抗体偶联的pulchellin,用共聚焦显微镜研究其在HIV感染细胞中的细胞内转运途径

Mohammad Sadraeian, F. M. Tsutae, H. H. Moreira, A. P. Araujo, F. G. Guimarães, S. Pincus
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摘要

Pulchellin是一种2型核糖体失活蛋白,从一些生长在巴西的种子中分离出来。它是一种抑制癌细胞和hiv感染细胞中蛋白质合成的有效药物。Pulchellin可与HIV单克隆抗体偶联,特异性靶向HIV感染细胞。为了分析Pulchellin对蛋白质合成的抑制作用,应将免疫偶联物的细胞内定位与Pulchellin进行比较。在这种情况下,细胞内这种蛋白质的运输可以通过共聚焦显微镜来确定。在我们的研究中,我们利用Pulchellin构建HIV单克隆抗体偶联的Pulchellin A链,以靶向HIV感染的淋巴细胞。然后用高级Alexa Fluor 488染料标记缀合物。作为后续步骤,我们有兴趣通过共聚焦显微镜研究这种新型偶联在hiv感染细胞中的细胞内运输途径。此外,可能的定量方法荧光标记免疫偶联物在共聚焦显微镜将进行研究。
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Preparation of HIV monoclonal antibody-conjugated pulchellin in order to study its intracellular trafficking pathway in HIV-infected cells by confocal microscopy
Pulchellin is a type 2 of ribosome-inactivating proteins isolated from some seeds significantly growing in Brazil. It is a potent agent to inhibit the protein synthesis in cancer cells and also HIV-infected cells. Pulchellin can be conjugated to HIV monoclonal antibodies to specifically target the HIV-infected cells. To analyze the protein synthesis inhibition by Pulchellin, the intracellular localization of the immunoconjugate should be compared to Pulchellin. In this case, the intracellular trafficking of this protein in cells can be determined by confocal microscopy. In our study, we utilized Pulchellin to construct HIV monoclonal antibody-conjugated Pulchellin A chain in order to target HIV-infected lymphocyte cells. Afterward the conjugation was labeled with the superior Alexa Fluor 488 dye. As a subsequent step, we are interested in studying the intracellular trafficking pathway of this novel conjugation in HIV-infected cells by confocal microscopy. Moreover, possible quantitative methods for fluorescent labeling of the immunoconjugate during confocal microscopy will be investigated.
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