Press Releases

Entry from: 19.02.2018
Category: News, Press Releases

A Matter of Dynamics

Most ion channels are very selective about the ions, which may or may not pass through them. They may be conductive for potassium ions and non-conductive for sodium ions or vice versa. However, a number of ion channels allows for the efficient passage of both kinds of ions. How do these channel proteins accomplish this? A team of scientists around Dr. Han Sun and the research group of Professor Adam Lange at the Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP) found the answer to this question. Their study revealed structural and dynamic differences between selective and non-selective ion channels. The scientists described their findings and conclusions in the journal Nature Communications. In non-selective channels, the selectivity filter exhibits sizeable dynamics, which are not present in selective channels. The selectivity filter of non-selective ion channels can exist in two different forms. Dependent on the state of the selectivity filter, one or the other ion type may pass.

Snapshot taken during the computer simulation of the NaK channel - This channel (shown in yellow and orange) enables the flow of ions (e.g. potassium ions [red spheres]) across the cell membrane. (The membrane lipids are depicted in gray.) Visualisation: Barth van Rossum, FMP.

Ion channels play prominent roles in organisms. For example, ion channels are in action when the organism registers stimuli and passes the information on to the brain in the form of electric signals. During this signal transmission, charged atoms (ions) must enter and leave the involved cells. Ions cannot permeate lipophilic cell membranes. Instead, they pass through protein channels in the cell membranes.

In many cases, the ion channels allow the passage of only one specific ion type, i.e. they may be conductive for potassium but not for sodium ions or vice versa. The selectivity filter that is the narrowest part of the channel is responsible for this ion discrimination. However, the NaK channel allows for the passage of both sodium and potassium ions. It was in the focus of the present study by FMP scientists around Dr. Han Sun and Professor Adam Lange together with colleagues in Göttingen (Germany) and Hefei (China).

Non-selective ion channels are very important in medicine.

Until now, it has remained controversial why NaK channels allow for the passage of both sodium and potassium ions. Professor Adam Lange explains: "While X-ray crystallographic images showed us the three-dimensional structure of the channel, it was difficult to explain why this channel is conductive to two different ion types with similarly high efficiency. This was particularly hard to understand because the sequence and the 3-D structure of the selectivity filter are similar to the ones in potassium selective channels."

Scientist Dr. Han Sun added that the investigated system is a model system for several other non-selective ion channels in the human body. As she pointed out, physiologically and medically relevant in this context are the cyclic nucleotide-gated and hyperpolarization-activated cyclic nucleotide–gated channels (CNG and HCN channels):  "We know that CNG channels are important for vision and smell. Dysfunctional HCN channels are implicated in various neurological diseases such as epilepsy or autism."

Specific Ions Prefer Specific Channel Structures

On their path to discovering how the non-selective NaK channel works, the scientists used a combination of nuclear magnetic resonance (NMR) spectroscopy and computer-assisted molecular dynamics simulations. The results revealed that the selectivity filter of the NaK channel dynamically changes between two structures. Each structure is conductive for one of the two ion types.
Dr. Han Sun reports: "Surprisingly, the computer simulations showed that potassium ions passing through the NaK channel prefer the structure of a potassium selective channel, while the mechanism of the sodium ion passage is similar to the passage of sodium ions through a sodium selective ion channel.” Until now, researchers believed that the structure of the selectivity filter is the same for sodium and potassium ion transport through the NaK channel.

To gather further evidence for the crucial role of the dynamic structure of the NaK selectivity filter, the scientists experimented with a mutated NaK channel (NaK2K double point mutation). This mutated NaK channel is conductive only for potassium ions. Professor Adam Lange gives an account of the results: "Our NMR investigations clearly revealed that the selectivity filter of this channel forms only a single structure."

Among other sources of financial support, the FMP scientists received funding from the DFG (Deutsche Forschungsgemeinschaft / German Research Foundation) as part of the funding for Research Group 2518 'Functional Dynamics of Ion Channels and Transporters'. The Norddeutscher Verbund für Hoch- und Höchstleistungsrechnen (HLRN; Northern German Association for Supercomputing) in Berlin allowed the FMP scientists to use their computing power. Conducting the molecular dynamics simulations would have been impossible without this assistance.

Chaowei Shi, Yao He, Kitty Hendriks, Bert L. de Groot, Xiaoying Cai, Changlin Tian, Adam Lange, Han Sun. A single NaK channel conformation is not enough for non-selective ion conduction, Nature Communications 19. Februar 2018, DOI 10.1038/s41467-018-03179-y


Dr. Han Sun
Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP)
Tel.: 0049 30 94062902

Prof. Dr. Adam Lange
Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP)
Tel.: 0049 30 94793-190

Public Relations
Silke Oßwald
Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP)
Tel.: +49-30-94793-104
E-Mail: osswald(at)

The Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP) is part of the Forschungsverbund Berlin e.V. (FVB), who legally represents eight non-university research institutes - members of the Leibniz Association - in Berlin. The institutions pursue common interests within the framework of a single legal entity while maintaining their scientific autonomy. More than 1,900 employees work within the research association. The eight institutes were founded in 1992 and emerged from former institutes of the GDR Academy of Sciences.

Leibniz-Forschungsinstitut für Molekulare Pharmakologie im Forschungsverbund Berlin e.V. (FMP)
Campus Berlin-Buch
Robert-Roessle-Str. 10
13125 Berlin, Germany
+4930 94793 - 100 
+4930 94793 - 109 (Fax)