Bruce Bean

Bruce Palmer Bean, PhD

Robert Winthrop Professor of Neurobiology

Neuronal Excitability and Ion Channel Pharmacology

Neurons communicate with each other using electrical impulses. Information is encoded as patterns of “action potentials”, millisecond-long reversals of the voltage across the cell membrane. Different neurons in the brain fire action potentials with a variety of distinct patterns. The Bean lab seeks to understand these different patterns of firing in terms of the underlying molecular devices – tiny pores in the membrane known as ion channels.

In mammalian brains, each neuron possesses several dozen different types of ion channels. Most of these are closed when the neuron is at rest (electrically silent). It is the coordinated, transient opening, or “gating” of particular types of ion channels that underlies electrical signaling. To understand how different combinations of ion channels work together to generate the distinct patterns of action potential firing in different neurons, we make electrical recordings of these cells using patch clamp, voltage clamp and other electrophysiological approaches.

Our goal is to use knowledge of the particular ion channels in different kinds of neurons to find new drugs that can selectively inhibit or enhance electrical activity of specific type of neurons by targeting specific ion channels. In collaboration with Dr. Clifford Woolf’s laboratory, we are currently focused on finding new drugs to treat pain, itch, and cough. We are also seeking to identify new drugs to disrupt epileptic activity.

Publications View
Inhibition of neuronal voltage-gated sodium channels by brilliant blue G.
Authors: Authors: Jo S, Bean BP.
Mol Pharmacol
View full abstract on Pubmed
Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors.
Authors: Authors: Bosmans F, Puopolo M, Martin-Eauclaire MF, Bean BP, Swartz KJ.
J Gen Physiol
View full abstract on Pubmed
A functionally characterized test set of human induced pluripotent stem cells.
Authors: Authors: Boulting GL, Kiskinis E, Croft GF, Amoroso MW, Oakley DH, Wainger BJ, Williams DJ, Kahler DJ, Yamaki M, Davidow L, Rodolfa CT, Dimos JT, Mikkilineni S, MacDermott AB, Woolf CJ, Henderson CE, Wichterle H, Eggan K.
Nat Biotechnol
View full abstract on Pubmed
Reference Maps of human ES and iPS cell variation enable high-throughput characterization of pluripotent cell lines.
Authors: Authors: Bock C, Kiskinis E, Verstappen G, Gu H, Boulting G, Smith ZD, Ziller M, Croft GF, Amoroso MW, Oakley DH, Gnirke A, Eggan K, Meissner A.
Cell
View full abstract on Pubmed
Incomplete inactivation and rapid recovery of voltage-dependent sodium channels during high-frequency firing in cerebellar Purkinje neurons.
Authors: Authors: Carter BC, Bean BP.
J Neurophysiol
View full abstract on Pubmed
Selectively targeting pain in the trigeminal system.
Authors: Authors: Kim HY, Kim K, Li HY, Chung G, Park CK, Kim JS, Jung SJ, Lee MK, Ahn DK, Hwang SJ, Kang Y, Binshtok AM, Bean BP, Woolf CJ, Oh SB.
Pain
View full abstract on Pubmed
Isolation of somatic Na+ currents by selective inactivation of axonal channels with a voltage prepulse.
Authors: Authors: Milescu LS, Bean BP, Smith JC.
J Neurosci
View full abstract on Pubmed
Pacemaking in dopaminergic ventral tegmental area neurons: depolarizing drive from background and voltage-dependent sodium conductances.
Authors: Authors: Khaliq ZM, Bean BP.
J Neurosci
View full abstract on Pubmed
Sodium channels gone wild: resurgent current from neuronal and muscle channelopathies.
Authors: Authors: Cannon SC, Bean BP.
J Clin Invest
View full abstract on Pubmed
Sodium entry during action potentials of mammalian neurons: incomplete inactivation and reduced metabolic efficiency in fast-spiking neurons.
Authors: Authors: Carter BC, Bean BP.
Neuron
View full abstract on Pubmed