Switching an Antibiotic On and Off with Light

Switching an Antibiotic On and Off with Light

By on Mar 22, 2014 in Biology, for featured, News | 0 comments

This image shows the painting of the Mona Lisa and also the image of the Mona Lisa in a petridish.

First, an inactivated photo-switchable antibiotic was added to a bacterial lawn. Then, a mask was applied and the lawn was exposed to light for the specific activation of the antibiotic. Credit Babii et al., Angewandte Chemie.

Fundamental research at KIT paves the way to the specific therapy of bacterial infections.

Scientists of the KIT and the University of Kiev have produced an antibiotic, whose biological activity can be controlled with light. Thanks to the robust diarylethene photoswitch, the antimicrobial effect of the peptide mimetic can be applied in a spatially and temporally specific manner. This might open up new options for the treatment of local infections, as side effects are reduced. The researchers present their photoactivable antibiotic with the new photomodule in a “Very Important Paper” of the journal Angewandte Chemie.

Photoswitchable molecules modify their structure and properties when exposed to light of an adequate wavelength. Among the photoswitches known are diarylethenes. By reversible photoisomerization, i.e. a reversible light-induced internal relocation of the molecule, the open form is turned into a closed form. Such photoswitch-able molecules are applied in molecular electronics and many other areas. Particularly interesting opportunities result from the insertion of photoswitches into biomolecules to control their activity by light. Interest focuses on so-called peptide mimetics, compounds whose major structural elements emulate a peptide, i.e. a small protein.

For the first time now, a group of researchers headed by Professor Anne S. Ulrich, Director of the Institute for Biological Interfaces 2 (IBG2) and holder of the Chair for Biochemistry at the Institute of Organic Chemistry (IOC) of KIT, has produced a photoswitchable peptide mimetic based on a diarylethene scaffold that can be photoisomerized reversibly. The scientists modified this building block into an amino acid analog and incorporated it directly into the backbone of the annular peptide antibiotic Gramicidin S. Biological activity of the resulting peptide mimetic can be controlled spatially and temporally with the help of UV and visible light. To demonstrate this, the scientists treated a bacterial film with the inactivated antibiotic and exposed it to light via a mask. As a result, the photoswitchable diarylethene was converted from a closed into an open form. Due to the structural modification induced, the entire substance molecule had a much higher antimicrobial effect. “In the future, such photoactivable antibiotics might be used as smart therapeutic agents against local bacterial infections,” Professor Anne S. Ulrich explains. “Usual side effects can also be minimized by switching.” Based on this strategy, new peptide-based agents against cancer might be feasible, as the newly developed photoactivable building block can also be applied in other peptide sequences.

About this biology article

Contact: Monika Landgraf – KIT
Source: KIT press release
Image Source: The image is credited to Babii et al./Angewandte Chemie and is adapted from the KIT press release
Original Research: Abstract for “Controlling Biological Activity with Light: Diarylethene-Containing Cyclic Peptidomimetics” by Oleg Babii, Sergii Afonin, Marina Berditsch, Sabine Reißer, Pavel K. Mykhailiuk, Vladimir S. Kubyshkin, Thomas Steinbrecher, Anne S. Ulrich, and Igor V. Komarov in Angewandte Chemie. Published online February 19 2014 doi:10.1002/ange.201310019

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