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Top neuroscientist Arthur Konnerth leaves Germany for full-time role in China

The Brain Prize winner, known for pioneering brain imaging techniques, joins the rapidly expanding Shenzhen Bay Laboratory

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Arthur Konnerth is a leading figure in neuroscience whose work has helped transform the understanding of how the brain processes information. Photo: Handout
Shi Huang
Arthur Konnerth, a recipient of the prestigious Brain Prize, has joined the Shenzhen Bay Laboratory (SZBL) on a full-time basis, the institute announced on January 29.
Konnerth is a leading figure in neuroscience whose work has helped transform the understanding of how the brain processes information. His research focuses on the fundamental mechanisms of learning and memory, employing a combination of electrophysiological, imaging and cellular techniques.

Konnerth pioneered the in vitro brain slice patch-clamp recording method – a technique that has become a cornerstone of modern neuroscience – and made fundamental discoveries in synaptic transmission and plasticity.

The technique uses a glass microelectrode to form a seal against the surface of a brain cell, preventing electricity from leaking away and allowing scientists to measure the electrical currents moving through a single “gate” in the cell’s membrane.

In 1989, Konnerth – working with Bert Sakmann, Frances Edwards and Tomoyuki Takahashi – helped transform the technique from concept to a standard method. They extended its use from isolated cells to neurons still connected within slices of brain tissue. This breakthrough laid the foundation for modern slice electrophysiology.

In 2003, he and his team introduced an imaging method that, for the first time, enabled scientists to watch entire networks of brain cells in action, seeing every individual cell at once. This technique is now widely used to study how the brain controls behaviour.

In 2010, the team pushed the technology even further, observing how a living mouse processes visual information at the level of individual synapses. They achieved this by combining a powerful laser-imaging technique called two-photon microscopy with their original electrical recording method. This allowed them to measure activity in a cell’s individual dendrites – the branch-like cables that receive incoming signals.

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