位置:成果数据库 > 期刊 > 期刊详情页
Mapping CD20 molecules on the lymphoma cell surface using atomic force microscopy
  • ISSN号:1001-6538
  • 期刊名称:Chinese Science Bulletin
  • 时间:0
  • 页码:-
  • 分类:Q26[生物学—细胞生物学] TH742[机械工程—光学工程;机械工程—仪器科学与技术;机械工程—精密仪器及机械]
  • 作者机构:[1]State Key Laboratory of Robotics, Shenyang Institute of Automation, Chinese Academy of Sciences, Shenyang 110016, China, [2]University of Chinese Academy of Sciences, Beijing 100049, China, [3]Department of Mechanical and Biomedical Engineering, City University ofHong Kong, Hong Kong, China, [4]Department of Lymphoma, Affiliated Hospital of Military Medical Academy of Sciences, Beijing 100071, China
  • 相关基金:This work was supported by the National Natural Science Foundation of China (60904095, 61175103), and the CAS FEA International Partnership Program for Creative Research Teams.
  • 相关项目:纳米操作机器人技术在癌症靶向治疗中的应用研究
中文摘要:

原子力量显微镜学(AFM ) 被用来在淋巴瘤 Raji 房间的表面上定位 CD20 分子。Rituximab (对 CD20 的 monoclonal 抗体) 分子经由聚乙烯乙二醇(木钉) 被连接到 AFM 尖端上连接器。Raji 房间被吸附到与 poly-L-lysine 涂的玻璃幻灯片上。首先,在房间表面的一个本地区域的 CD20 分发用 AFM 电梯扫描模式被设想。第二, 16

英文摘要:

Atomic force microscopy (AFM) was used to locate CD20 molecules on the surface of lymphoma Raji cells. Rituximab (a mono- clonal antibody against CD20) molecules were linked onto the AFM tip via a polyethylene glycol (PEG) linker. Raji cells were adsorbed onto glass slides coated with poly-L-lysine. First, the CD20 distribution in a local area of the cell surface was visualized using the AFM lift scan mode. Second, 16 x 16 force curves were obtained from the same cell area to construct the CD20- rituximab binding force map. Finally, free rituximab was added to block the CD20 molecules on the cell surface and the lift phase image and CD20-rituximab force map were obtained again. The experimental results indicated that when the lift height was great- er than the length of the PEG linker, no recognition sites were observed in the lift phase image. However, as the lift height de- creased to the length of the PEG linker, some recognition sites were observed in the lift phase image and these sites were general- ly consistent with the pixels in the force map. After blocking, both the recognition sites in the lift phase image and the gray pixels in the binding force map decreased markedly. These results can improve our understanding of the distribution of protein mole- cules on the cell surface and facilitate further investigations into cellular functions.

同期刊论文项目
期刊论文 30 会议论文 24 获奖 7 专利 2
期刊论文 73 会议论文 22 获奖 92
同项目期刊论文