Affinity probe capillary electrophoresis of insulin using a fluorescence‐labeled recombinant Fab as an affinity probe

Affinity probe CE (APCE) separates and detects a target molecule as a complex using a fluorescence‐labeled affinity probe (AP) by CE. The electrophoretic separation of the complex ensures accurate identification of a specific signal among nonspecific ones, which often compromises the credibility of immunoassays. APCE of insulin using a recombinant Fab (rFab) as an AP was demonstrated as a model system in this report. Anti‐insulin rFab was expressed in Escherichia coli and labeled at a cysteine residue in the hinge region with a thiol‐reactive rhodamine dye. Electrophoretically pure labeled rFab was recovered from a focused band in slab‐gel IEF and used as an AP. A mixture of standard insulin and the AP with carrier ampholyte was introduced into a neutral‐polymer coated fused silica capillary (50 μm id, 120 mm long). IEF was carried out at 500 V/cm, and the capillary was scanned for laser‐induced fluorescence under focusing conditions. The insulin‐AP complex focused at pH 6.6 within 6 min along with the free AP at pH 7.6. The complex peak decayed according to the first‐order reaction kinetics with a half life of 3.8 min. A linear calibration line was obtained for standard insulin at a concentration range of 20 pM to 5 nM using the AP at 50 nM. These results demonstrate that rFab is useful for the preparation of an AP for APCE.