Measuring the molecular force of Burkitt's lymphoma patient cells using AFM

Mi Li, Lianqing Liu, N. Xi, Yuechao Wang, Z. Dong, Guangyong Li, Xiubin Xiao, Weijing Zhang
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Abstract

The treatment of Non-Hodgkin's lymphoma (NHL) was revolutionized by the approval of rituximab in 1997. Rituximab is a CD20-directed monoclonal antibody (mAb). Despite the great success of rituximab in the treatment of B-cell NHL, the urgent need is to enhance the efficacy due to the markedly variable patient responses. Hence elucidating the molecular mechanisms of rituximab's anti-cancer effect is of great significance. In the past decade the atomic force microscopy (AFM) has proven to be a powerful tool for characterizing the morphological properties and measuring the physiological interaction forces of single cells and single molecules under native conditions. In this work, the AFM single-molecule force spectroscopy(SMFS) was applied to quantitatively measure the CD20-rituximab binding force on Burkitt's lymphoma patient bone marrow cells. The experimental results will facilitate further investigation of the molecular mechanisms of rituximab's anticancer effect.
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利用原子力显微镜测量伯基特淋巴瘤患者细胞的分子力
1997年利妥昔单抗(rituximab)获批后,非霍奇金淋巴瘤(NHL)的治疗发生了革命性的变化。利妥昔单抗是一种cd20定向单克隆抗体(mAb)。尽管利妥昔单抗在治疗b细胞NHL方面取得了巨大成功,但由于患者反应的显著差异,迫切需要提高疗效。因此阐明利妥昔单抗抗癌作用的分子机制具有重要意义。在过去的十年中,原子力显微镜(AFM)已被证明是表征单细胞和单分子在自然条件下的形态特性和测量生理相互作用力的有力工具。本研究采用AFM单分子力谱法(SMFS)定量测定cd20 -利妥昔单抗对伯基特淋巴瘤患者骨髓细胞的结合力。实验结果将有助于进一步研究利妥昔单抗抗癌作用的分子机制。
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