New influenza viruses jump from animals to humans with alarming frequency, as evidenced by the H5N1 bird flu virus or, more recently, with the swine flu virus. Although humans usually do not have any preexisting immunity to such pathogens, they are not completely unprotected against the invaders. The human body can rapidly mobilize a defense strategy which prevents the influenza viruses from proliferating unchecked in the body.
An essential element of this protection is a protein, known as Mx (short for myxovirus resistance), produced by the body which recognizes many viruses and prevents them from replicating inside infected cells. Under normal conditions this protective protein is not present in the cell at all, but after infection it can be produced in large quantities. The order to produce this protein Mx is made by the signaling protein interferon, which is excreted by infected cells and alarms the organism of the virus infection.
Mx is a molecular machine which does not develop its full power until the individual molecules have joined to form a ring-structured macromolecular network. A central element of the formation of these ring structures is the special part of Mx known as the stalk.
Scientists have attempted to describe the structure of this stalk for years. The virologists Otto Haller, Alexander von der Malsburg, and Georg Kochs in Freiburg and the structural biologists Oliver Daumke, Song Gao, Susann Paeschke, and Joachim Behlke from MDC in Berlin-Buch have now unraveled the secret of the stalk structure of Mx at the atomic level. This structure explains the composition of Mx and allows scientists to conduct tests to make predictions concerning the mode of action of the antiviral molecule.
In combination with findings from earlier biochemical studies, the results of this study make it clear that the stalk structure of Mx functions as a kind of clamp which restrains and deactivates important components of the influenza virus in the infected cell. The fact that new forms of flu can lead to epidemics or even pandemics in spite of this defense mechanism is due to the power and aggressiveness of these pathogens.
The researchers are confident that their new findings about the protective Mx protein will form the basis for the development of new antiviral drugs for combating dangerous influenza viruses. Moreover, they are also certain that this new knowledge about the function of Mx will increase their understanding of other members of this family of proteins.
*Structural basis of oligomerisaton in the stalk region of dynamin-like MxA
Song Gao1,2, Alexander von der Malsburg3, Susann Paeschke1, Joachim Behlke1, Otto Haller3, Georg Kochs3, Oliver Daumke1
1Max Delbrück Center for Molecular Medicine, Crystallography, Robert-Rössle-Strasse 10, 13125 Berlin, Germany
2Institute for Chemistry and Biochemistry, Free University Berlin, Takustrasse 3, 14195 Berlin, Germany
3Department of Virology, Institute of Medical Microbiology and Hygiene, University of Freiburg, Hermann-Herderstrasse 11, 79104 Freiburg, Germany
Dr. Oliver Daumke
Max Delbrück Center for
Molecular Medicine (MDC) Berlin-Buch
Phone: +49-30-94 06-34 25
Fax: +4930-94 06-38 14
Prof. Dr. Otto Haller
Freiburg University Medical Center
Institute of Medical Microbiology
and Hygiene; Department of Virology
Phone: +49 761 203 65 34
Fax: +49 761 203 66 26