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Feature Articles : Mar 15, 2012 ( )
Harnessing Innovation to Improve Expression Systems
Technical advances in the use of protein-expression systems have enabled scaled production of membrane proteins and other difficult to express proteins. These advances have also helped preserve the structure and function of the expressed proteins.
Shuguang Zhang, Ph.D., associate director of the Center for Biomedical Engineering at MIT, has found that the use of short peptide surfactants in commercial E. coli cell-free systems facilitates the rapid production of membrane proteins.
GPCRs, the most difficult integral membrane proteins to produce, can be produced in milligram quantities when the right surfactant is added to the cell-free system. The soluble GPCRs that Dr. Zhang’s team has produced show a-helical secondary structures, which suggest proper folding; ligand binding studies have confirmed the maintenance of biological function.
“I am convinced that the use of short, simple peptide surfactants is absolutely the key for successful production of membrane proteins in cell-free systems,” he says. “Further, the use of cell-free systems allows for industrial-scale standardization of protein production. We have demonstrated its utility on GPCRs. If we can just reduce the cost 10–20 fold in the next decade, I have no doubt you’ll see an increase in its use for protein production.”
The benefit of using cell-free systems is the ease of use and the ability to add components to promote protein production and stability. These cell-free systems can be maintained for a long time, though they are not amenable to repeat production.
As for the addition of peptide surfactants, it is essential to screen different surfactants to ensure matching with each individual membrane protein for optimal production. The peptide surfactants that have been used are designed with a hydrophilic head (1–2 residues) and a hydrophobic tail (3–6 residues). They are usually 2–3 nm in length, their ionic character and strength can be controlled by selection of the intervening residues.
The surfactants have a tendency to self-assemble to form membrane-like environments that provide stability for the membrane proteins, even though the mechanism remains unclear.
Joining Dr. Zhang as a presenter at the upcoming “PEGS” conference in Boston will be Mark Welch, Ph.D., director of gene design at DNA2.0.
DNA2.0’s custom gene design and synthesis service enables customers to obtain optimal protein expression for their gene of interest, according to Dr. Welch. The company is guided by informatics and experimental studies of the effect of gene usage on heterologous protein expression from different expression and production hosts (bacterial, yeast, and mammalian cells). From this analysis, the company has developed robust algorithms that predict optimal gene sequences that will provide abundant protein yields.
At present, DNA2.0 has turned its attention to the application of these tools for optimal production of pharmaceutical target proteins in mammalian hosts. “We have developed solid algorithms for production of a variety of proteins in bacteria and yeast systems,” Dr. Welch explained. “We are now focused on building that same level of knowledge in mammalian cell systems.”
Working with an academic partner, DNA2.0 is also exploring the optimization of protein expression of difficult to express membrane proteins as well as the effects of gene sequence on expression level and localization in differentiated mammalian tissues.
Dr. Welch will also talk about Infologs™, non-natural gene variants that are designed through informatics to capture maximal structure/function correlations in the biological space of interest. DNA2.0’s research demonstrates how the technique leads to uniform sampling, systemic variance, and unrestricted information-rich results.
Recombinant Mammalian Proteins
Ashok Bandaranayake, Ph.D., associate in the department of biochemistry at the Albert Einstein College of Medicine, will discuss Daedalus, which was developed for rapid production of recombinant mammalian proteins in human cell culture. Dr. Bandaranayake started this work when he was at the Seattle Children’s Hospital Research Institute.
He is currently optimizing Daedalus for a high-throughput protein production effort as part of the Protein Structure Initiative (New York Structural Genomics Consortium). He employs the Lentivirus system, which can be used to efficiently transduce human cells.
This low copy number vector (10–20 copies per genome) also has package-size limitations. With clones greater than 10 kb the viral titer drops significantly, and it has been observed that efforts to increase the copy number often result in a net negative result with increased promoter silence when incorporated into the genome.
Dr. Bandaranayake has overcome the low copy number by using a strong promoter (from spleen focus forming virus). He has overcome promoter silence observation by adding a minimized ubiquitous chromatin opening element. These GC-rich sequences exist as islands of 8 kb, 4 kb, or 2 kb, all of which impact the package-size limitations.
Dr. Bandaranayake has also cloned a 0.7 kb element that is equally effective in keeping expression levels high. To effectively overcome the package-size limitation, Dr. Bandaranayake has demonstrated that cells can be co-infected with vectors containing different subunits of a large protein.
These subunits have been shown to readily self-assemble in the positively transfected cells. The final trick is the cloning of signal peptide encoding sequences upstream of the gene of interest to make sure the produced recombinant protein is secreted into the media.
Protein secretion ensures that the protein is folded correctly and makes for easy purification. Proteins purified from serum-free media come off as a single peak from gel filtration columns. “We use serum-free adapted HEK293 cells for production of the recombinant proteins,” Dr. Bandaranayake notes.
“We have demonstrated the utility of this system using soluble immune receptors, six different human cytokines, and most recently two canine cytokines that are used in transplant studies. This approach is not applicable for membrane proteins as the essential element is the secretion of the protein product. You would have to mutate the membrane-binding domains to make sure the integral membrane protein didn’t get hung up in the membrane. By the time you’ve done that you’ve destroyed the structure/function paradigm.”
Blood Coagulation Factors
Liang Tang, Ph.D., senior scientist of molecular biology and protein expression at Bayer Healthcare, is using the Lentivirus system for large-scale production of functional proteins in a family of blood coagulation factors that tends to express poorly in mammalian cells.
The team is working on producing coagulation factors for research using BHK21 cells, which proved optimal for production of factor VIII; this should eliminate any variation related to post-translational modifications. Lentiviral vectors allow rapid and reliable production of protein candidates in this cell line, which is not routinely used for rapid protein production.
In his presentation, Dr. Tang will discuss resource management—the time and manpower needed to produce candidate therapeutic proteins. “We have improved our approach to protein expression, which has resulted in a Lentivirus-transduced stable pool that can be harvested in weeks instead of months,” he explains.
“The Lentivirus-transduced stable pools can be frozen down and revived in culture when we’ve found a good therapeutic candidate. In this way we have a constant supply of the protein for further analysis. We grow our positive cultures in a 10–20 L Wave bioreactor (GE Healthcare). I am confident that the lessons learned from our effort with coagulation factors can be applied to other proteins and protein families.”
Brian Kloss, Ph.D., senior scientist at the New York Consortium on Membrane Protein Structure (NYCOMPS), will discuss optimization of high-throughput solutions for cloning, expression, and purification of integral membrane proteins in bacteria.
Dr. Kloss prepares protein candidates for functional and structural analysis by others in the consortium. Earlier phases of this work focused on representative proteins from each of approximately 175 families of bacterial membrane proteins.
Proteins are assigned to a family if they show 50–60% amino acid identity. From this group, 28 structures have been solved to date. Contrast that with the human proteome, where there are approximately 700 families of human membrane proteins.
“We have made technical and methodological improvements over the years and employ automation at each step in the process, so that we can now simultaneously prepare and analyze large numbers of samples. This includes the use of the cloning technique called ligation independent cloning and optimization of small-scale protein expression, using 2 mL blocks. The wells in the blocks will support growth of 600 µL to 1 mL cultures, which yields enough to run the protein product out on a gel for an initial screen.”
“I have to say that cell lysis is perhaps the most critical step when dealing with integral membrane proteins. We have helped develop a robotic sonicator arm that can safely and effectively lyse the cells without perturbing the protein within the membrane.” The process occurs in two rounds of sonication for a total of 15–20 minutes per 96-well plate.
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