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Hydrophobic Interaction Chromatography for Biopharmaceutical Analysis

Hydrophobic interaction chromatography (HIC) is a milder form of reversed phase liquid chromatography (RPLC).  Separation of analytes is based on hydrophobic interactions with the stationary phase; therefore, the elution order in HIC enables proteins to be ranked on the basis of their relative hydrophobicity.  HIC employs non-denaturing conditions, does not require the use of organic solvents or high temperatures, and separations are carried out at physiological pH allowing the preservation of protein structure.  Historically HIC has been used for the determination of the relative hydrophobicity of proteins and was applied on a preparative scale for protein purification; it is now applied at all stages of the purification process including, high-yield capture, polishing monoclonal antibodies (mAbs), characterization of mAbs and antibody-drug-conjugates, removal of truncated species from full-length forms, separation of active and inactive forms, and clearing viruses.

HIC analysis is carried out using a reversed salt gradient, starting with a high salt concentration and moving to low salt concentration to facilitate protein elution.  When starting at high salt concentration proteins are retained on the stationary phase because the hydrophobic interaction between the solute and stationary phase is increased due to salt in the buffer reducing the solvation of the proteins; as solvation decreases hydrophobic regions become exposed and are adsorbed to the stationary phase.  The more hydrophobic the molecule the less salt is needed to promote binding. 

The mobile phase is typically an aqueous solution of a non-denaturing salt such as ammonium sulfate (1-2 M) or sodium chloride (3 M) and a buffer to control pH (usually phosphate, 6 ≤ pH ≤ 7).  High concentrations of salt, especially ammonium sulfate, may precipitate proteins; therefore, solubility should be checked under the initial gradient (binding) conditions.  The strength of the interaction between the protein and stationary phase decreases with increasing pH as a result of increased charge on the protein due to the ionization of acidic groups.  This effect can vary depending on the protein, thus, pH can impact the level of protein binding and selectivity.  Changes in pH do not have a significant effect over moderate ranges.

Stationary phases generally consist of silica bonded with ligands of relatively limited hydrophobicity (butyl, phenyl, ether, amide, propyl).  Straight chain alkyl ligands exhibit hydrophobic character, whereas aryl ligands provide mixed-mode behavior where both aromatic and hydrophobic interactions are possible.  The choice of ligand type will be determined empirically.  Normally stationary phases are non-porous; however, there are also some porous polymethacrylate-based particles available.  HIC columns can be operated at pressures in the range 100-400 bar, and are typically packed with 5, 3, or 2.5 µm particles.

HIC can be applied to the analysis of mAb heterogeneity resulting from post-translational modifications (Table 1).  HIC has found particular applicability to the analysis of antibody drug conjugates (ADCs).  ADCs contain a lipophilic cytotoxic drug attached to a mAb; the mAb affords the selectivity while the drug provides the efficiency of treatment.  Separation occurs since most cytotoxins are hydrophobic.  The hydrophobicity of the ADC depends on the number of conjugated drugs; therefore, ADCs with different drug-to-antibody ratios (DAR) can be separated in HIC.  In terms of elution order, mAbs which contain no drug will be eluted first with those with the highest number of drugs attached eluted last.  The relative distribution of the ADC species can be determined on the basis of peak area percentages.  The weighted DAR can then be determined based in the percentage peak area information and the drug load numbers.  Due to the high salt concentrations used HIC is generally incompatible with MS detection (although successful studies have implemented HIC-MS analysis of intact proteins using ammonium tartrate as a MS-compatible salt in place of the more traditional ammonium sulfate).  Multidimensional chromatography utilizing an RPLC desalting step prior to MS analysis allows online characterization of ADCs as the ADCs dissociate into their respective sub units under the denaturing RPLC conditions. 

Modification HIC Peak
Aspartate isomerization Pre-peak
Asparagine deamidation Post-peak + pre-peak
Oxidation Pre-peak
PyroGlu from Glu (─H2O) Post-peak
PyroGlu from Gln (─NH3) Post-peak
Succinimide Post-peaks
Sugar Pre-peak
C-terminal lysine Pre-peak
Aggregation Post-peak
Fragmentation Variable

Table 1: Common PTMs, with expected retention times relative to the principal intact protein peak.

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Dr. Dawn Watson
 

This article was written by Dr. Dawn Watson.

Dawn received her PhD in synthetic inorganic chemistry from the University of Strathclyde, Glasgow. The focus of her PhD thesis was the synthesis and application of soft scorpionate ligands. As well as synthetic skills, this work relied on the use of a wide variety of analytical techniques, such as, NMR, mass spectrometry (MS), Raman spectroscopy, infrared spectroscopy (IR), UV-visible spectroscopy, electrochemistry, and thermogravimetric analysis.

Following her PhD she spent two years as a postdoctoral research fellow at Princeton University studying the reaction kinetics of small molecule oxidation by catalysts based on Cytochrome P450. In order to monitor these reactions stopped-flow kinetics, NMR, HPLC, GC-MS, and LC-MS techniques were utilized.

Prior to joining the Crawford Scientific and CHROMacademy technical team she worked for Gilson providing sales and support for the entire product range including, HPLC (both analytical and preparative), solid phase extraction, automated liquid handling, mass spec, pipettes, and laboratory consumables.

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