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Purification of hepatitis B surface antigen by affinity chromatography
Vox Sanguinis
|January 1, 1978
Summary
This study presents a simple and rapid method for purifying Hepatitis B surface antigen (HBsAg) from plasma. The technique achieves high purity and recovery, making it suitable for large-scale production.
Area of Science:
- Biochemistry
- Virology
- Biotechnology
Background:
- Hepatitis B virus (HBV) infection is a significant global health concern.
- Hepatitis B surface antigen (HBsAg) is a key component of HBV and a target for diagnostics and vaccines.
Purpose of the Study:
- To develop an efficient and scalable purification method for Hepatitis B surface antigen (HBsAg).
- To characterize the purified HBsAg particles.
Main Methods:
- Purification of HBsAg from human plasma using affinity chromatography with matrix-bound sulphated carbohydrates (heparin or dextran sulphate).
- Further purification of HBsAg via precipitation with polyethylene glycol (PEG) 6000.
- Characterization of purified HBsAg using electron microscopy.
Main Results:
- A highly purified HBsAg preparation was obtained.
- The purification process yielded approximately 70% recovery of the total antigen.
- Electron microscopy confirmed the presence of predominantly 22 nm spherical particles, with minimal filamentous forms.
Conclusions:
- The described method provides a simple, rapid, and effective means for purifying HBsAg.
- This purification technique is well-suited for large-scale applications in vaccine or diagnostic development.