NsXeR protein: A new optogenetic tool to control muscle and neuronal cells

Sep 30 2017

Scientists have examined a protein that will find application in optogenetics and could be used to control muscle and neuronal cells. The paper on the light-sensitive NsXeR protein of the xenorhodopsin class was published in Science Advances by the international team of researchers from MIPT, Research center Jülich, and Institut de Biologie Structurale.

Why it matters

Optogenetics is a new technique that uses light to control neurons or muscle cells in living tissue. It has found wide application in nervous system studies. Optogenetic manipulations are so precise that they make it possible to control individual neurons by switching certain information transfer pathways on or off. Similar methods are also used to partially reverse eyesight or hearing loss as well as to control muscle contractions.

The main tools of optogenetics are light-sensitive proteins that are intentionally inserted into particular cells. After the insertion, the protein gets into the cell surface and moves ions across the membrane upon exposure to light. Thus, in a modified neuron cell, a correctly chosen light impulse may activate a neural signal or, on the contrary, suppress all the signals, depending on which protein is used. By activating signals from individual neurons, it is possible to imitate the functioning of certain brain regions — a technique that modulates the behavior of the organism under study. If such proteins are inserted in muscle cells, an external signal can tense or relax them.

The authors of the paper, which was published in Science Advances, described a new optogenetic tool — a protein called NsXeR, which belongs to the class of xenorhodopsins. When exposed to light, it can activate individual neurons, making them send set signals to the nervous system. Apart from applications in nervous system research, xenorhodopsins may also take over muscle cell control. To activate these cells, it is preferable that calcium ion transport be blocked, because alterations in the ion concentration can affect them. When using proteins that transport various positive ions (such as calcium) nonselectively, undesirable side effects are likely to appear.

The discovered protein helps to bypass uncontrolled calcium translocation: It is selective and pumps nothing but the protons into the cell. Because of this selectivity, it has a considerable advantage over its chief competitor channelrhodopsin, which is being extensively used in research but does not discriminate between positively charged ions. What is more, xenorhodopsin acts as a reliable pump, transporting protons into the cell regardless of their concentration, whereas channelrhodopsin only allows ions to move from an area of higher concentration to an area of lower concentration. In both cases a positive charge inflow into an excitable cell reduces the voltage difference between its inner and outer membrane surfaces. Such membrane depolarization generates a nerve or muscle impulse. The ability to induce such an impulse by pumping nothing but protons will reduce possible side effects during research.

“So far we have all the necessary data on how the protein functions. This will become the basis of our further research aimed at optimizing and adjusting the protein parameters to the needs of optogenetics,” says Vitaly Shevchenko, the lead author of the paper and a staff member at the MIPT Laboratory for Advanced Studies of Membrane Proteins.

This research was supported ERA.Net RUS PLUS and the Ministry of Education and Science of the Russian Federation (project ID 323, RFMEFI58715X0011).