Automated buffer preparation using quaternary valve in fast performance liquid chromatography for protein purification from a cell membrane

J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Jan 1:1136:121849. doi: 10.1016/j.jchromb.2019.121849. Epub 2019 Nov 12.

Abstract

There is a great need for high-throughput protein purification to produce protein molecules for research and therapeutics. Although there have been significant advancements made in automated multi-step chromatography and preparative in-process design-of-experiment (DOE) capabilities in commercial fast performance liquid chromatography (FPLC) instruments, almost all commercial FPLCs rely on a binary buffer mixing system, which hinders automated buffer preparation. Nevertheless, current-generation FPLCs are equipped with a quaternary mixer designed for limited in-line buffer preparation and preparative pH scouting DOE experiments. We decided to leverage the quaternary mixing capability by extending and re-programming AkTA Avant's quaternary valve into an automated in-process buffer preparation system to simplify automated purification requiring complex washing steps. We accomplished this by using two extra inlet valves, a sample valve, and versatile valve to split inputs of the quaternary valve into software-selectable stock solutions of pH buffers, salts, eluents, and additives. We also devised a new flow scheme to perform automated two-step chromatography using only one versatile valve. This was accomplished by using only stock parts and software to facilitate reproduction. To demonstrate the versatility and capability of the system, we purified a transmembrane protein that requires a detergent to stay soluble and needs an in-column, high-salt washing step to achieve high purity.

Keywords: AkTA; Automated buffer preparation; Automated chromatography; High-throughput purification; Multi-dimensional chromatography.

MeSH terms

  • Automation, Laboratory / instrumentation*
  • Buffers
  • Cell Membrane / chemistry*
  • Chromatography, Liquid / instrumentation*
  • Chromatography, Liquid / methods
  • Equipment Design
  • Humans
  • Membrane Proteins / isolation & purification*

Substances

  • Buffers
  • Membrane Proteins