Tangential flow filtration (TFF) is widely used in biopharmaceutical processing for protein purification – a common application for TFF is ultrafiltration for concentration/diafiltration of proteins. In this type of application, the product protein is retained (concentrated) within the feed side of the ultrafiltration membrane, while the buffer components and other small impurities (smaller than the membrane pore size) freely pass through the membrane into the permeate side. Several scholarly articles are available in literature which discuss the ultrafiltration application as well as its optimization strategies. Another category of application where TFF finds significant use is in the clarification of cell culture bioreactor and microbial fermenter feed solutions using microfiltration membranes. In some of these microfiltration TFF applications (e.g., mammalian cell culture clarification), the product (protein) freely passes through the microfiltration membrane and is recovered on the permeate side, while the contaminating impurities (cells, cell debris, colloids) are retained on the feed side of the membrane. In certain other microfiltration TFF applications (allantoic fluid clarification in egg-based flu process), the product (flu virus) may get concentrated on the feed side of the microfiltration membrane (similar to an ultrafiltration step), while the contaminating impurities (ovalbumin, etc.) may get removed into the permeate side…
Tag: <span>protein purification</span>
Since its beginnings in the 1970s, recombinant DNA technology has become integral in the production of pharmaceutically important proteins such as blood factors, hormones, growth factors, interferons, interleukins, and vaccines. Recombinant technology was developed in Escherichia coli, and because of its long history of use and ease of manipulation, the bacteria remains a common expression system. However, E. coli is limited in the types of proteins it can express, and production can be hampered by the formation of intracellular inclusion body aggregates which complicate the processes of protein recovery and purification. The non-pathogenic Corynebacterium glutamicum can accumulate amino acids extracellularly and has historically been used for the commercial production of amino acids glutamate and lysine. More recently, C. glutamicum has been developed as an expression system with the ability to secrete properly folded, functionally active proteins into the fermentation broth. Production in C. glutamicum has the same advantages of scalability and ease of culturing as in E. coli, but with more simplified recovery and purification processes…
Sea lice are the most problematic marine pathogens the salmon industry has to deal with, significantly affecting Europe and America. The worst offenders are genera: Pseudocaligus, Caligus, and Lepeophtheirus. Over €305 million in losses are estimated. Recent results have suggested that subolesin/akirin/myosin32 are good candidate antigens for the control of arthropod infestations such as sea lice. The aim of this study was to design and optimize the purification step of MY32/Ls protein to obtain the active pharmaceutical ingredient against sea lice. Non-chromatographic purification strategies were employed, based on published works, to establish rupture, washing, solubilization, and refolding conditions…
Cation exchange chromatography is typically utilized in bind-and-elute mode for monoclonal antibody purification. However, during purification process development for a novel monoclonal antibody (MAb) intended for clinical use, it was determined that bind-and-elute conditions were not sufficient for removing significant levels of antibody aggregate. Based on preliminary purification data, an alternative purification method, operation of the cation exchange process in flow-through mode, was investigated.