Crystal Structure of the Mammalian GIRK2 K+ Channel and Gating Regulation by G Proteins, PIP2, and Sodium

SummaryG protein-gated K+ channels (Kir3.1–Kir3.4) control electrical excitability in many different cells. Among their functions relevant to human physiology and disease, they regulate the heart rate and govern a wide range of neuronal activities. Here, we present the first crystal structures of a G protein-gated K+ channel. By comparing the wild-type structure to that of a constitutively active mutant, we identify a global conformational change through which G proteins could open a G loop gate in the cytoplasmic domain. The structures of both channels in the absence and presence of PIP2 suggest that G proteins open only the G loop gate in the absence of PIP2, but in the presence of PIP2 the G loop gate and a second inner helix gate become coupled, so that both gates open. We also identify a strategically located Na+ ion-binding site, which would allow intracellular Na+ to modulate GIRK channel activity. These data provide a structural basis for understanding multiligand regulation of GIRK channel gating.

Graphical AbstractFigure optionsDownload full-size imageDownload high-quality image (308 K)Download as PowerPoint slideHighlights► Structures of GIRK2 in the absence and presence of PIP2 and Na+ were solved ► A constitutively active mutant suggests a mechanism for G protein regulation ► Without PIP2, G proteins appear to open only the cytoplasmic domain gate ► Together, PIP2 and G proteins appear to couple the opening of both channel gates