Subunit structure of islet-activating protein, pertussis toxin, in conformity with the A-B model

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Abstract
The subunit structure of islet-activating protein (IAP), pertussis toxin, was analyzed to study a possibility that this protein is one of the A-B toxins. Heating IAP with 1% sodium dodecyl sulfate caused its dissociation into 5 dissimilar subunits named S-1 (MW 28,000), S-2 (23,000), S-3 (22,000), S-4 (11,700) and S-5 (9300), as revealed by polyacrylamide gel electrophoresis; their molar ratio in the native IAP was 1:1:1:2:1. The MW of IAP estimated by equilibrium ultracentrifugation was 117,000 which was not at variance with the value obtained by summing up MW of the constituent subunits. The preparative separation of theses IAP subunits was next undertaken; exposure of IAP to 5 M ice-cold urea for 4 days followed by column chromatography with CM-Sepharose caused sharp separation of S-1 and S-5, leaving the other subunits as 2 dimers. These dimers were then dissociated into their constituent subunits, i.e., S-2 and S-4 for 1 dimer and S-3 and S-4 for the other, after 16-h exposure to 8 M urea; these subunits were obtained individually upon further chromatography on a DEAE-Sepharose column. Subunits other than S-1 were adsorbed as a pentamer by a column using haptoglobin as an affinity adsorbent. The same pentamer was obtained by adding S-5 to the mixture of 2 dimers. Neither this pentamer nor other oligomers (or protomers) exhibited biological activity in vivo. Recombination of S-1 with the pentamer at the 1:1 molar ratio yielded a hexamer which was identical with the native IAP in electrophoretic mobility and biological activity to enhance glucose-induced insulin secretion when injected into rats. In the broken-cell preparation, S-1 was biologically as effective as the native IAP; both catalyzed ADP-ribosylation of a protein in membrane preparations from rat C6 glioma cells. IAP is an oligomeric protein consisting of an A (active) promoter (the biggest subunit) and a B (binding) oligomer which is produced by connecting 2 dimers by the smallest subunit in a noncovalent manner. Rationale for this terminology is discussed based on the A-B model.

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