Development of a novel alpha7-nicotinic acetylcholine receptor-selective cell-penetrating peptide for intracellular cargo transport.

Drug delivery into the brain remains a critical barrier for the treatment of neurological diseases. While the brain is shielded from many toxins and viruses by the blood-brain barrier (BBB), therapeutics are being created that exploit natural bypass mechanisms by forming complexes with cell-penetrating peptides (CPPs) derived from viruses. Neurological diseases often impact specific proteins in the brain; however, current CPPs lack the ability to selectively target precise cellular macromolecules. As a result, they are distributed broadly throughout the brain and cause off-target side effects. Neurotropic CPPs derived from the rabies virus glycoprotein (RVG) can access the brain by binding to plasma membrane targets, including, but not exclusively, nicotinic acetylcholine receptors (nAChRs). To overcome this barrier of minimal target selectivity, we designed several chimeric peptides composed of regions from the RVG and α-bungarotoxin, an α7 subtype-selective protein. Using human nAChRs expressed in