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RUB researchers decode the interplay between enkephalins and pain receptors

Metal complex arrests elusive messenger

Ruhr-University Bochum


IMAGE: The enkephalin receptor (gray) threads through the cell membrane. The structure of the free enkephalin in the complex with the rhodium atom (orange) is highlighted in green. view more

Credit: Florian Wieberneit (Biomolecular NMR)

"Pain begone!" In order to send out this signal, the human body produces tiny messenger molecules that dock to certain receptors. Using traditional biochemical methods, this interaction between the messengers, so-called enkephalins, and opioid receptors is very difficult to study. An interdisciplinary team of biochemists and inorganic chemists at the Ruhr-Universität Bochum (RUB) has now succeeded in identifying the structure of an enkephalin in solution and to track its interaction with the opioid receptor in detail. The analysis provides a new, precise starting point for the development of drugs meant to combat specific types of pain. This discovery is featured in the cover story of the Dalton Transactions journal.

Rhodium facilitates analysis of enkephalins in solution

Enkephalin is a peptide; it is made up of amino acids. Because it is very flexible in solution, researchers find it difficult to "grasp" the tiny molecule for the purpose of structural analysis. RUB chemists have deployed a trick: they have introduced a complex into the enkephalin that contains the precious metal rhodium and does not occur in nature. Subsequently, they have analysed the structure of the metal-peptide complex by means of nuclear magnetic resonance (NMR). With bound rhodium, it was possible to study the enkephalin much more extensively than ever before. Using computer simulation, the researchers then calculated how to optimally integrate the specific structure of the enkephalin, as identified by means of NMR spectroscopy, into the established three-dimensional structure of the receptor.

40 years after the discovery

Enkephalins were the first neuropeptides to be discovered and researched, but that did not happen until the 1970s. Related opioid receptors, members of the category of so-called G protein-coupled receptors, have eluded structural analysis for many decades, however. It was not until last year that some of their structures were decoded; moreover, the 2012 Nobel Prize in Chemistry being awarded for studies of G protein-coupled receptors has given this particular research field a new boost. "All of a sudden - some 40 years after enkephalins were discovered - we begin to understand on a nuclear level how these messengers bind to their receptors," says Prof Dr Nils Metzler-Nolte, head of the RUB research team Medicinal Inorganic Chemistry. "Our research shows that, by deploying metal complexes that do not occur in nature, we help solving questions in the field of medicine that have long remained unanswered," adds Prof Dr Raphael Stoll from the research team Biomolecular Spectroscopy.


Financial backing and groundwork

The research at hand is supported by the German Research Foundation (Deutsche Forschungsgemeinschaft; FOR 630 and SFB 642). It has its roots in the collaboration between the teams of Nils-Metzler Nolte and Raphael Stoll and Prof Dr Richard H. Fish of the Lawrence Berkeley National Laboratory in California. In the previous year, the team demonstrated for the first time how metal complexes can be deployed in structural analysis.

Bibliographic record

F. Wieberneit, A. Korste, B. Albada, N. Metzler-Nolte, R. Stoll (2013): Structural and biological implications of the binding of Leu-enkephalin and its metal derivatives to opioid receptors, Dalton Transactions, DOI: 10.1039/C3DT50635E

Further information

Prof Dr Nils Metzler-Nolte
Inorganic Chemistry I, Faculty of Chemistry and Biochemistry at the Ruhr-Universität
44780 Bochum, Germany, phone +49/234/32-24153

Prof Dr Raphael Stoll
Biomolecular Spectroscopy, Faculty of Chemistry and Biochemistry at the Ruhr-Universität
44780 Bochum, Germany, phone +49/234/32-25466

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Previous press information re.: metal-peptide complexes

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Editor: Dr Julia Weiler

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