Multimerization and Aggregation of Native-State Insulin: Effect of Zinc
2012
Xu, Yisheng | Yan, Yunfeng | Seeman, Daniel | Sun, Lianhong | Dubin, Paul L.
The aggregation of insulin is complicated by the coexistence of various multimers, especially in the presence of Zn²⁺. Most investigations of insulin multimerization tend to overlook aggregation kinetics, while studies of insulin aggregation generally pay little attention to multimerization. A clear understanding of the starting multimer state of insulin is necessary for the elucidation of its aggregation mechanism. In this work, the native-state aggregation of insulin as either the Zn–insulin hexamer or the Zn-free dimer was studied by turbidimetry and dynamic light scattering, at low ionic strength and pH near pI. The two states were achieved by varying the Zn²⁺ content of insulin at low concentrations, in accordance with size-exclusion chromatography results and literature findings (Tantipolphan, R.; Romeijn, S.; Engelsman, J. d.; Torosantucci, R.; Rasmussen, T.; Jiskoot, W.J. Pharm. Biomed. 2010, 52, 195). The much greater aggregation rate and limiting turbidity (τ∞) for the Zn–insulin hexamer relative to the Zn-free dimer was explained by their different aggregation mechanisms. Sequential first-order kinetic regimes and the concentration dependence of τ∞ for the Zn–insulin hexamer indicate a nucleation and growth mechanism, as proposed by Wang and Kurganov (Wang, K.; Kurganov, B. I.Biophys. Chem. 2003, 106, 97). The pure second-order process for the Zn-free dimer suggests isodesmic aggregation, consistent with the literature. The aggregation behavior at an intermediate Zn²⁺ concentration appears to be the sum of the two processes.
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