Imaging and mapping individual target proteins on clinical lymphoma cells by AFM

Mi Li, Lianqing Liu, N. Xi, Yuechao Wang, Wenxue Wang
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引用次数: 1

Abstract

The wide applications of atomic force microscopy (AFM) in the past decade have contributed much to the field of cell biology, providing a lot of novel insights into cellular behaviors at the nanoscale. However, current AFM studies are commonly performed on cell lines cultured in vitro which are quite different from the cells in the human body. Directly investigating the physiological activities on tumor cells from clinical patients is of great significance for helping us to better understand the actual cellular activities taking place in the clinical environment. Under the fluorescence recognition of specific tumor cell surface marker, we have used AFM to investigate the binding affinity and nanoscale distributions of CD20 target protein directly on tumor cells prepared from the bone marrow of lymphoma patients. The results provide a new idea to develop closer links between laboratory study and clinical practice, which may have potential impacts on diverse fields such as drug evaluation and efficacy prediction.
利用原子力显微镜对临床淋巴瘤细胞的单个靶蛋白进行成像和定位
近十年来,原子力显微镜(AFM)的广泛应用为细胞生物学领域做出了巨大贡献,为纳米尺度上的细胞行为提供了许多新的见解。然而,目前的AFM研究通常是在体外培养的细胞系上进行的,这些细胞系与人体细胞有很大的不同。直接研究临床患者肿瘤细胞的生理活动,对于帮助我们更好地了解临床环境中实际发生的细胞活动具有重要意义。在特异性肿瘤细胞表面标记物的荧光识别下,我们利用原子力显微镜研究了CD20靶蛋白直接在淋巴瘤患者骨髓制备的肿瘤细胞上的结合亲和力和纳米级分布。该研究结果为进一步加强实验室研究与临床实践的联系提供了新的思路,并可能对药物评价和疗效预测等多个领域产生潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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