Antigen purification
Disclosed herein are methods and exemplary compositions associated with antigen purification, exemplary aspects of which may include harvesting viral and antigenic substances from source organisms; and a purification platform comprising chemical separation and size-difference separation for the removal of contaminants, debris and impurities from the viral and protein (e.g. antigenic, including influenza hemagglutinin antigens) substances, as well as their concentration and collection.
1. A method for purifying at least one antigen harvested from a source organism, comprising:
extracting cellular debris from the at least one antigen by adding an extraction buffer to an extract at a ratio of the extraction buffer and the extract expressed as extraction buffer:extract by wt;
after the extracting step, concentrating the at least one antigen by passing the at least one antigen through a tangential flow filtration apparatus; and
performing separations comprising sub-steps of separating host cell contaminants from the at least one antigen, subjecting the at least one antigen to affinity chromatography to elute the at least one antigen, and after the separating host cell contaminants and affinity chromatograph sub-steps, subjecting the at least one antigen to multi-modal chromatography to separate residual impurities from the at least one antigen.
2. The method of claim 1 , wherein the source organism is a plant.
3. The method of claim 2 , further comprising harvesting the at least one antigen from the plant.
4. The method of clam 1 , further comprising harvesting the at least one antigen from the source organism, wherein the source organism is selected from the group consisting of bacterial, algal, yeast, insect, and mammalian organisms.
5. The method of claim 1 , wherein extracting cellular debris from the at least one antigen comprises passing the at least one antigen through a membranous filtration device comprising a porous membrane.
6. The method of claim 5 , wherein the method further comprises maintaining a feed pressure of less than thirty pounds per square inch across the porous membrane.
7. The method of claim 1 , wherein said ratio is in a range between 1:1 and 2:1.
8. The method of claim 1 , wherein the method further comprises establishing a transmembrane pressure across the filter between about 10-20 psi.
9. The method of claim 1 , wherein separating host cell contaminants from the at least one antigen comprises subjecting the at least one antigen to ion-exchange chromatography.
10. The method of claim 1 , wherein subjecting the at least one antigen to affinity chromatography comprises subjecting the at least one antigen to cobalt immobilized metal affinity chromatography.
11. The method of claim 1 , wherein subjecting the at least one antigen to multi-modal chromatography comprises subjecting the at least one antigen to a ceramic hydroxyapatite chromatography column.