A multiplexed microfluidic toolbox for the rapid optimization of affinity-driven partition in aqueous two phase systems

• Published in: Journal of Chromatography A 2017-09, Vol.1515, p.252-259
• Main Authors: Bras, Eduardo J.S., Soares, Ruben R.G., Azevedo, Ana M., Fernandes, Pedro, Arévalo-Rodríguez, Miguel, Chu, Virginia, Conde, João P., Aires-Barros, M. Raquel
• Format: Article
• Language: English
• Subjects: Affinity tags; Antibodies; Aqueous two-phase systems; LYTAG; Microfluidics; Rapid screening
• ISSN: 0021-9673
• DOI: 10.1016/j.chroma.2017.07.094

•A microfluidic chip for simultaneously screening eight independent ATPS is presented.•Eight conditions were tested under using less than 20μL of each solution.•A second chip for testing back extraction steps was also developed.•PEG-phosphate ATPS conditions were tested to optimize the affinity partition of GFP-LYTAG.•Extraction of IgG using LYTAG-Z affinity tags is optimized and demonstrated. Antibodies and other protein products such as interferons and cytokines are biopharmaceuticals of critical importance which, in order to be safely administered, have to be thoroughly purified in a cost effective and efficient manner. The use of aqueous two-phase extraction (ATPE) is a viable option for this purification, but these systems are difficult to model and optimization procedures require lengthy and expensive screening processes. Here, a methodology for the rapid screening of antibody extraction conditions using a microfluidic channel-based toolbox is presented. A first microfluidic structure allows a simple negative-pressure driven rapid screening of up to 8 extraction conditions simultaneously, using less than 20μL of each phase-forming solution per experiment, while a second microfluidic structure allows the integration of multi-step extraction protocols based on the results obtained with the first device. In this paper, this microfluidic toolbox was used to demonstrate the potential of LYTAG fusion proteins used as affinity tags to optimize the partitioning of antibodies in ATPE processes, where a maximum partition coefficient (K) of 9.2 in a PEG 3350/phosphate system was obtained for the antibody extraction in the presence of the LYTAG-Z dual ligand. This represents an increase of approx. 3.7 fold when compared with the same conditions without the affinity molecule (K=2.5). Overall, this miniaturized and versatile approach allowed the rapid optimization of molecule partition followed by a proof-of-concept demonstration of an integrated back extraction procedure, both of which are critical procedures towards obtaining high purity biopharmaceuticals using ATPE.