A purified polyclonal antibody (IgG) is separated and fully characterized using the Viscotek SEC-MALS 20, allowing calculation of molecular weight and radius of gyration (Rg).
Therapeutic recombinant antibodies represent a growing proportion of biopharmaceuticals and are primarily classed as Immunoglobulin G (IgG). However, proteins have a tendency to aggregate over time and one challenge for biologic drugs is that the presence of aggregates will stimulate an immune response. Size-exclusion chromatography (SEC) is a powerful tool that is commonly used to look at the aggregation of proteins. While most SEC systems use a single concentration detector such as ultraviolet (UV), the addition of light scattering allows the molecular weight of the protein to be measured independent of its retention volume. The new SEC-MALS 20 detector, which uses multi-angle light scattering (MALS), is ideal for this application. In addition, the MALS detector makes it possible to measure the radius of gyration (Rg) of molecules that scatter light anisotropically.
The SEC-MALS results are presented in Table I. The monomer (15.80 mL) and dimer (14.00 mL) peaks are clearly identified by the measured molecular weights and low polydispersity (Mw/Mn). No size (Rg) can be measured for these peaks as they are below the isotropic scattering threshold of 10–15 nm. Studying Figure 1, it is just possible to see that the SEC-MALS 20 show the same response for the monomer peaks at all angles. The aggregate peak (13.23 mL) is clearly different. The molecular weight is higher and more polydisperse, which shows that there is a variable composition of molecules within the aggregate peak. Because it is large, the light scattering response varies with angle and can be used to measure the Rg.
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