Title: The β Subunit of the High Conductance Calcium-activated Potassium Channel
Abstract: Coexpression of α and β subunits of the high conductance Ca<sup>2+</sup>-activated K<sup>+</sup>(maxi-K) channel leads to a 50-fold increase in the affinity for<sup>125</sup>I-charybdotoxin (<sup>125</sup>I-ChTX) as compared with when the α subunit is expressed alone (Hanner, M., Schmalhofer, W. A., Munujos, P., Knaus, H.-G., Kaczorowski, G. J., and Garcia, M. L. (1997) <i>Proc. Natl. Acad. Sci. U. S. A.</i>94, 2853–2858). To identify those residues in the β subunit that are responsible for this change in binding affinity, Ala scanning mutagenesis was carried out along the extracellular loop of β, and the resulting effects on <sup>125</sup>I-ChTX binding were determined after coexpression with the α subunit. Mutagenesis of each of the four Cys residues present in the loop causes a large reduction in toxin binding affinity, suggesting that these residues could be forming disulfide bridges. The existence of two disulfide bridges in the extracellular loop of β was demonstrated after comparison of reactivities of native β and single-Cys-mutated subunits to<i>N</i>-biotin-maleimide. Negatively charged residues in the loop of β, when mutated individually or in combinations, had no effect on toxin binding with the exception of Glu<sup>94</sup>, whose alteration modifies kinetics of ligand association and dissociation. Further mutagenesis studies targeting individual residues between Cys<sup>76</sup> and Cys<sup>103</sup> indicate that four positions, Leu<sup>90</sup>, Tyr<sup>91</sup>, Thr<sup>93</sup>, and Glu<sup>94</sup> are critical in conferring high affinity<sup>125</sup>I-ChTX binding to the α·β subunit complex. Mutations at these positions cause large effects on the kinetics of ligand association and dissociation, but they do not alter the physical interaction of β with the α subunit. All these data, taken together, suggest that the large extracellular loop of the maxi-K channel β subunit has a restricted conformation. Moreover, they are consistent with the view that four residues appear to be important for inducing an appropriate conformation within the α subunit that allows high affinity ChTX binding.