Researchers at the Faculty Mathematics and Natural Sciences of the the University of Groningen and of the University Medical Center Groningen have exposed a new shortcut by which membrane proteins are guided to the inner nuclear membrane. Unlike in the method known hitherto, the protein’s ‘address code’ is found to be attached to a long string that wriggles, as it were, through the membrane pore. This discovery is to be published online in the journal Science Express on 9 June at 9 p.m.
The Groningen researchers studied how particular membrane proteins find their way to the right place in a cell. The cell nucleus and the nuclear pore complexes are present in all plant, animal and human cells, and their function is vital to life: if they malfunction, the cell dies. Fundamental research of this kind is an investment in the future and in this particular case will probably have applications in medicine.
Being in the right place at the right time is very important to a protein: timing and location are crucial if it is to do its job. This is not a new realization, and in the case of many proteins we already know how and when they reach the correct location. Often there is a signal encoded on the surface of the protein: particular transport proteins recognize this ‘address code’ and can then take the protein to the right place in the cell.
The location that the researchers were interested in is the membrane on the inside of the cell nucleus, the nucleus that also contains the DNA. To get there, proteins need to be guided in via transport channels, the nuclear pores. What the Groningen researchers have unearthed now is an address code completely different from the address codes for transport via the nuclear pores known hitherto. The newly discovered address code is suspended from a long so-called ‘linker’. Cooperation between the first three authors, Anne Meinema, Justyna Laba and Astri Hapsari, was the key to success. The code is specific to certain proteins in the membrane around a cell nucleus.
The long, flexible linker is able to extend and fold up easily and thus to take the address code a long way from the membranes. The linker wriggles its way through the nuclear pore complex so that the address code, to which the transport proteins are attached, can pass through the channel efficiently. Thus a new shortcut through the nuclear pore complex has been discovered.
Shown here are two nuclear pore complexes (purple and blue) in the membrane around the nucleus and the route that a membrane protein (yellow) takes to reach the inside of the nucleus. It can be seen how how transport proteins (red and purple) recognize the address code at the end of the long linker. The linker wriggles its way through the nuclear pore complex so that the transport proteins can pass through the channel.
• Contact: Dr Liesbeth Veenhoff, tel. 050-363 4187; l.m.veenhoff rug.nl
• Article: Long Unfolded Linkers Facilitate Membrane Protein Import Through the Nuclear Pore Complex in Science, 9 June 2011• Authors: Anne C. Meinema, Justyna K. Laba, Rizqiya A. Hapsari, Renee Otten, Frans A. A. Mulder, Annemarie Kralt, Geert van den Bogaart, C. Patrick Lusk, Bert Poolman, Liesbeth M. Veenhoff• Departments involved: Biochemistry and Biophysical Chemistry, University of Groningen; Neuroscience, University Medical Center Groningen; Cell Biology, Yale School of Medicine, USA
The Dutch Research Council (NWO) has awarded 32 experienced researchers a Vici grant worth € 1.5 million each. Three of the awardees are conducting research at the University of Groningen (UG), and two at the University Medical Center Groningen (UMCG)...
This afternoon, the University of Groningen started using a piezo testing ground at the Stationspark (station park) in Zuidhorn.