This video demonstrates a technique for purifying monoclonal antibodies from the culture supernatant obtained from an antibody-producing cell culture. The process involves using a matrix of crosslinked agarose beads with conjugated Protein A, which immobilizes the antibodies in the supernatant on the beads, allowing for effective separation from contaminants. By applying an elution buffer with low pH, the protein A-antibody interaction is loosened, facilitating the collection of antibody-containing fractions.
Protocol
1. Antibody Purification by Affinity Chromatography Using an Automated Fast Protein Liquid Chromatography (FPLC) System NOTE: The following procedure can generally be applied to most automated systems. Purification can be performed at room temperature or at 4 °C (if FPLC system is kept in a cool room). A series of scouting tests can be performed to identify the optimal purification conditions including appropriate column matrix, binding buffer, elution buff…
Disclosures
The authors have nothing to disclose.
Materials
Phosphate Buffered Saline (PBS) Tablets, pH 7.4, 100 ml
09-2051-100
Astral Scientific
HiTrap Protein A High Performance, 1 x 5 ml column
GE17-0403-01
Sigma-Aldrich
AKTApurifier 100
28406266
GE Healthcare
Automated FPLC system, which can include a P-960 sample pump and Frac-920 fraction collector.
Glycine-HCl
G2879
Sigma-Aldrich
Citric Acid, monohydrate
BIOC2123
Astral Scientific
Sodium Citrate, trisodium salt dihydrate
BIOCB0035
Astral Scientific
1 M Tris-HCl solution pH 9.0
BIOSD8146
Astral Scientific
Amicon Ultra Centrifugal Filters (30 MWCO)
UFC803008/UFC903008
Merck Millipore
Used to buffer exchange and concentrate purified protein.
Pierce Bicinchoninic Acid (BCA) Assay Kit
23227
Thermo Fisher Scientific
BLItz System
45-5000
fortéBIO
Instrument used for bio-layer interferometry (BLI) measurements.