Magnetic, Molecular & Genetic Interfaces

Magnetogenetics

Magnetogenetics is the umbrella term for controlling genetically-defined neurons with externally applied magnetic fields, which pass through bone and tissue essentially unattenuated and require no implanted light source, wire, or electrode. It couples a field to a molecular transducer — most credibly a synthetic magnetic nanoparticle, more controversially an engineered iron-storage protein — that in turn gates a genetically-expressed ion channel, so that only cells carrying the transgene respond.

The field spans three physically distinct mechanisms: magnetothermal (heat dissipated by nanoparticles in an alternating field gating a thermosensitive channel), magnetomechanical (force or torque on particles gating a mechanosensitive channel), and disputed single-protein schemes built on ferritin. Its appeal is that magnetism offers the deepest, least-invasive write channel known; its liability is that the force a laboratory field can exert on a nanoscale magnetic object is extremely small, so proposed mechanisms and their reproducibility must be scrutinised with unusual care.

Treat magnetothermal actuation with synthetic nanoparticles as physically sound and demonstrated in rodents, and single-protein ferritin schemes as unresolved and contested — do not conflate them under one optimistic headline.

Also called
magnetic control of neuronsmagnetically-actuated neuromodulation