Detecting CD20-Rituximab specific interactions on lymphoma cells using atomic force microscopy

• Published in: Science China. Life sciences Vol. 53; no. 10; pp. 1189 - 1195
• Main Authors: Li, Mi, Liu, LianQing, Xi, Ning, Wang, YueChao, Dong, ZaiLi, Li, GuangYong, Xiao, XiuBin, Zhang, WeiJing
• Format: Journal Article
• Language: English
• Published: Beijing Science China Press 01.10.2010; Springer Nature B.V
• Subjects: Antibodies, Monoclonal, Murine-Derived - metabolism; Antigen-Antibody Complex - metabolism; Antigens, CD20 - metabolism; Antineoplastic Agents - metabolism; Binding Sites; Biomedical and Life Sciences; Cell Line, Tumor; Cell Membrane - immunology; Cell Membrane - metabolism; Humans; Life Sciences; Lymphoma, B-Cell - immunology; Lymphoma, B-Cell - metabolism; Microscopy, Atomic Force; Microscopy, Fluorescence; Research Papers; Rituximab; CD20 antigen; Rituximab; single-molecule force spectroscopy; atomic force microscopy
• ISSN: 1674-7305; 1869-1889
• DOI: 10.1007/s11427-010-4070-9

Elucidating the underlying mechanisms of cell physiology is currently an important research topic in life sciences. Atomic force microscopy methods can be used to investigate these molecular mechanisms. In this study, single-molecule force spectroscopy was used to explore the specific recognition between the CD20 antigen and anti-CD20 antibody Rituximab on B lymphoma cells under near-physiological conditions. The CD20-Rituximab specific binding force was measured through tip functionalization. Distribution of CD20 on the B lymphoma cells was visualized three-dimensionally. In addition, the relationship between the intramolecular force and the molecular extension of the CD20-Rituximab complex was analyzed under an external force. These results facilitate further investigation of the mechanism of Rituximab’s anti-cancer effect.