Transient receptor potential (TRP) channels exhibit a feature of forming multimeric and heteromeric complexes between intra-and inter-members of TRP family.
The pore and gate regions of voltage-gated cation channels have been often targeted with drugs acting as channel modulators.In contrast, the voltage sensing
Membrane fusion and fission events in intracellular trafficking are controlled by both intraluminal Ca2+ release and phosphoinositide (PIP) signalling.Howev