They are composed of a pore-forming α-subunit associated with up to four known different β-subunits. The tetrodotoxin

(TTX)-sensitive Na+ channels are classified according to sequence homology as Nav1.1 to Nav1.7 and they are differentially distributed in the central and peripheral nervous MAPK inhibitor system, in skeletal muscle, and in cardiac muscle. VGSC and K+ channels dysfunction (channelopathies) can result in neuromuscular diseases and heart or brain disorders such as arrhythmias and epilepsy [1], [14] and [18]. Mutations in the genes encoding for Nav1.1 and Nav1.2 isoforms have been linked to various forms of epilepsy and febrile seizures [21]. Thus, the key role of VGSCs in many tissues makes them important targets for pharmacological and biophysical studies, especially by dissecting the specific toxin–channel interactions. The investigation on the pharmacology of sodium channel toxins from sea anemones started more than SB431542 price 30 years ago [4] and [26], and further studies on site-directed mutagenesis took place later in the 1990s [11], [15], [16] and [25].

Nevertheless, very few information on electrophysiological and selectivity effects in a broader range of channels was reported [6] and [23]. Sea anemone type 1 toxins are peptides whose binding sites in VGSCs partially overlap with those of α-scorpion toxins. Their actions involve almost completely and selectively to induce a particular delay in ion channel conformational change called inactivation (transition from the open to the shut state) as opposed to the early process of activation (opening of the Na+-selective pore). This inactivated state is distinct from the closed state and there are many different methods to manipulate it from the intracellular side, either by using enzymes [2], drugs, point mutations (for a review see Ulbricht [33]) and specific toxins

from venomous animals. In the present paper, we studied three sea anemone type 1 toxins (CGTX-II, δ-AITX-Bcg1a and δ-AITX-Bcg1b) purified from the venom of the sea anemone Bunodosoma cangicum. Two Atazanavir of those toxins (δ-AITX-Bcg1a and δ-AITX-Bcg1b) differ in only one amino acid (N16D), but their potencies are markedly different. Also, in contrast to CGTX-II, both δ-AITX-Bcg1a and δ-AITX-Bcg1b have substitutions at positions 36–38. These positions were reported, in other sea anemone toxins, to be involved in the toxin–channel interaction, then inducing a robust increase in the slow component of the inactivation [5], [25], [28] and [31], which is the origin of the physiological prolongation of the action potential.