The conjugation of three amine reactive fluorescent probes, each containing the fluorophore fluorescein but different reactive moieties, was compared using the protein myoglobin and the amino acid L-lysine as reagents. The three different reactive moieties were an isothiocyanate group (FITC), a succinimidyl ester group (CFSE), and a dichlorotriazine group (DTAF). The relative performance was based on the degree of conjugation to myoglobin, the rate of reaction, freedom from hydrolysis, and the stability of a conjugate with lysine. Performance was evaluated by separating the conjugation reaction reagents and products on-line, using capillary zone electrophoresis, and assessing relative amounts by absorbance detection. Each of the reactive probes demonstrated the ability to achieve a similar degree of conjugation, which depended mostly on allowed conjugated reaction time, and a rate of conjugation that rendered hydrolysis of the reactive moiety insignificant. For the relative rate of conjugation between probes and stability of the resulting conjugate, CFSE demonstrated superior performance, followed by DTAF and then FITC, for both the protein myoglobin and the amino acid L-lysine. The FITC conjugation reaction was much easier to control, however, which may be significant for applications that require a precise degree of conjugation. With regard to conjugate-bond stability, the FITC conjugate demonstrated inferior performance when subjected to incubation at 37 degrees C.

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The biotechnology industry has undergone rapid growth in recent years largely due to the development and success of protein-based therapeutics for a wide range of disorders. Similar to traditional pharmaceuticals, characterization of a therapeutic protein for its physicochemical properties, process monitoring and lot release is crucial. Electrophoresis in the slab-gel format has and continues to be a mainstay of the protein laboratory; and more recently, CE has begun to make significant inroads for protein analysis in industrial settings. This review focuses on the electrophoresis of proteins with an emphasis on protein-based therapeutics in the capillary, slab-gel and to a lesser extent, the microchip format. Reported applications of electrophoresis at several stages of the biopharmaceutical industry covering the period of 2000-2005 will be discussed.

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Solution-phase immunoassays based on capillary electrophoresis (CE) separations have been shown to be rapid and simple to perform. The potential for sample matrix interference and incompatibility with multiplexing conditions for antibody detection when dealing with real samples, however, has prompted the development of an assay that utilizes an immunosubtraction methodology. A model assay for the detection of specific antibodies that relies on solid-phase extraction, CE and laser-induced fluorescence (LIF) detection is described. The method, called immunocapture-immunosubtraction (ICIS), incorporates an antibody capture/purification protocol using magnetic particles. The detection of specific antibodies is achieved by CE-LIF analysis of a probe solution following incubation with the captured antibodies. As an example of the ICIS assay's capabilities, the relative quantification of anti-fluorescein in serum is presented.

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