Editing Affinity chromatography (section)

==Batch and column setups==
[[File:Affinity chromatoraphy english.svg|thumb|Principle of affinity column chromatography]]
[[Image:batch.jpg|170px|right|thumb|Batch chromatography]]
Binding to the solid phase may be achieved by column chromatography whereby the solid medium is packed onto a column, the initial mixture run through the column to allow settling, a wash buffer run through the column and the elution buffer subsequently applied to the column and collected. These steps are usually done at ambient pressure. Alternatively, binding may be achieved using a batch treatment, for example, by adding the initial mixture to the solid phase in a vessel, mixing, separating the solid phase, removing the liquid phase, washing, re-centrifuging, adding the elution buffer, re-centrifuging and removing the elute.

Sometimes a hybrid method is employed such that the binding is done by the batch method, but the solid phase with the target molecule bound is packed onto a column and washing and elution are done on the column.

The ligands used in affinity chromatography are obtained from both organic and inorganic sources. Examples of biological sources are serum proteins, lectins and antibodies. Inorganic sources are moronic acid, metal chelates and triazine dyes.<ref>{{Cite book|title=Liquid Chromatography: Applications|series=Handbooks in Separation Science|editor1=Fanali, Salvatore|editor2=Haddad, Paul R.|editor3=Poole, Colin F.|editor4=Schoenmakers, Peter|editor5=Lloyd, David|publisher=Elsevier|year=2013|isbn=9780124158061|location=Saint Louis|page=3}}</ref>

A third method, expanded bed absorption, which combines the advantages of the two methods mentioned above, has also been developed. The solid phase particles are placed in a column where liquid phase is pumped in from the bottom and exits at the top. The gravity of the particles ensure that the solid phase does not exit the column with the liquid phase.

Affinity columns can be [[Elution|eluted]] by changing salt concentrations, pH, pI, charge and ionic strength directly or through a gradient to resolve the particles of interest.

More recently, setups employing more than one column in series have been developed. The advantage compared to single column setups is that the resin material can be fully loaded since non-binding product is directly passed on to a consecutive column with fresh column material. These chromatographic processes are known as [[periodic counter-current chromatography]] (PCC). The resin costs per amount of produced product can thus be drastically reduced. Since one column can always be eluted and regenerated while the other column is loaded, already two columns are sufficient to make full use of the advantages.<ref>{{cite journal |last1=Baur |first1=Daniel |last2=Angarita |first2=Monica |last3=Müller-Späth |first3=Thomas |last4=Steinebach |first4=Fabian |last5=Morbidelli|first5=Massimo |year=2016 |title=Comparison of batch and continuous multi-column protein A capture processes by optimal design |journal=Biotechnology Journal |volume=11 |issue=7 |pages=920–931 |doi=10.1002/biot.201500481 |pmid=26992151 |hdl=11311/1013726 |s2cid=205492204 |hdl-access=free }}</ref> Additional columns can give additional flexibility for elution and regeneration times, at the cost of additional equipment and resin costs.