Measurement of sialic acid content on recombinant membrane proteins
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KeywordsSialic Acid Potassium Channel Clonal Isolate Stable Pool EDTA Free Protease Inhibitor Cocktail
Membrane proteins such as cell adhesion molecules, receptors, transporters and ion channel proteins all have essential roles in cell-growth, migration, and flow of information, cell-cell and cell-protein communication. Membrane proteins are targets of biopharmaceutical companies because they have diverse effects on the progression of many diseases . Ion channels are membrane proteins that play critical roles in a number of cell functions including communication and neuromuscular activity. Treatment of channelopathy diseases such as cancer, cardiac arrhythmia, ataxia, paralysis, epilepsy, memory and learning loss, requires a broad understanding of ion channel function. Sialic acid is a critical charged glycan that affects the action potential of potassium channels which leads to changes in the neuronal system of organisms. In order to understand the effect of the sialylation on channel function, the presence of the sialic acid on the protein of interest should be studied. In this study, a novel method for the quantification of sialic acid is described for a potassium channel membrane protein.
Materials and methods
HEK293 cells were grown in DMEM media (Invitrogen, Carlsbad, CA) supplemented with 10% Fetal Bovine Serum (Invitrogen), 1% nonessential amino acids (Invitrogen) and 1% L-Glutamine (Invitrogen).
LipofectamineTM 2000 Reagent (Invitrogen) was used to transfect potassium channel into HEK293 cells. Stable pools were formed after 15 days of antibiotic selection and 8 different clones were selected from the pools.
Western blot analysis
Cells were lysed in RIPA buffer containing complete-mini EDTA free protease inhibitor cocktail (Roche Diagnostics, Mannheim, Germany). The protein concentrations of each sample were determined by using a BCA™ protein assay kit (Pierce, Rockford, IL). Equal total protein amounts were loaded onto 8% gels and separated by electrophoresis. The separated proteins were transferred from the gel to membrane. For detection of the channel protein, membrane was incubated in 1% milk in PBST solution containing primary antibody with a dilution of 1:1000 overnight at 4°C. A secondary anti-rabbit IgG HRP conjugate antibody (Amersham, Louisville, CO) was used at a dilution of 1:5000 in 1% milk/PBST overnight at 4°C.
The potassium channel protein was purified by using G-beads coupled antibody.
The purified protein was run on the gel and protein band was cut from the gel. The cut band was acid hydrolyzed to release the sialic acid. The released sialic acid was derivatized with fluorescent 4,5-Methylenedioxy-1,2-phenylenediamine dihydrochloride (DMB) reagent and injected to HPLC .
Membrane proteins are to be very difficult to produce and purify for structural or glycan analysis because of their low expression levels. In this study, HEK 293 cells were used to express a potassium channel protein and clonal isolates were picked from stable pools to evaluate the quality and quantity of the glycosylated protein. A highly expressing clone with glycosylation was then selected for the purification and sialic acid analysis. The results showed that the sialic acid occupancy efficiency of the channel of interest was around 80% when expressed in HEK293 cells.
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