Abstract

Atomic force microscopy (AFM) was used to locate CD20 molecules on the surface of lymphoma Raji cells. Rituximab (a monoclonal 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 × 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 greater than the length of the PEG linker, no recognition sites were observed in the lift phase image. However, as the lift height decreased to the length of the PEG linker, some recognition sites were observed in the lift phase image and these sites were generally 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 molecules on the cell surface and facilitate further investigations into cellular functions.

Highlights

  • Atomic force microscopy (AFM) was used to locate CD20 molecules on the surface of lymphoma Raji cells

  • The disturbance of the cellular topography is eliminated, and the lift scan trace is only influenced by the specific antibody–antigen binding between CD20 on the cell surface and rituximab on the tip

  • When rituximab binds to CD20, the amplitude of the cantilever changes and leads to changes in the phase information of the lift scan phase image, and CD20 on the cell surface can be visualized in the lift scan image

Read more

Summary

Introduction

Atomic force microscopy (AFM) was used to locate CD20 molecules on the surface of lymphoma Raji cells. By tethering antibodies or ligands onto the AFM tip, specific molecules (receptors or antigens) on the cell surface can be located by using either binding force mapping [10] or dynamic force recognition mapping [11]. We combined the AFM lift scan method and the binding force mapping method to locate CD20 molecules on the surface of lymphoma Raji cells.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call