Ion channels allow ions to pass through cell membranes by forming aqueous permeation pathways (pores). In contrast to most known ion channels, which have single pores, a chloride channel belonging to the ClC family (Torpedo ClC-0) has functional features that suggest that it has a unique ‘double-barrelled’ architecture in which each of two subunits forms an independent pore. This model is based on single-channel recordings of ClC-0 that has two equally spaced and independently gated conductance states^,,. Other ClC isoforms do not behave in this way,, raising doubts about the applicability of the model to all ClC channels. Here we determine the pore stoichiometry of another ClC isoform, human ClC-1, by chemically modifying cysteines that have been substituted for other amino acids located within the ClC ion-selectivity filter. The ClC-1 channel can be rendered completely susceptible to block by methanethiosulphonate reagents when only one of the two subunits contains substituted cysteines. Thiol side chains placed at corresponding positions in both subunits can form intersubunit disulphide bridges and coordinate Cd²⁺, indicating that the pore-forming regions from each subunit line the same conduction pathway. We conclude that human ClC-1 has a single functional pore.