Tuberculosis is one of the top ten causes of death worldwide, and due to the appearance of drug-resistant strains, the development of new antituberculotic agents is a pressing challenge. Employing an in silico docking method, two coumaran (2,3-dihydrobenzofuran) derivatives—TB501 and TB515—were determined, with promising in vitro antimycobacterial activity. To enhance their effectiveness and reduce their cytotoxicity, we used liposomal drug carrier systems. Two types of small unilamellar vesicles (SUV) were prepared: multicomponent pH-sensitive stealth liposome (SUVmixed) and monocomponent conventional liposome. The long-term stability of our vesicles was obtained by the examination of particle size distribution with dynamic light scattering. Encapsulation efficiency (EE) of the two drugs was determined from absorption spectra before and after size exclusion chromatography. Cellular uptake and cytotoxicity were determined on human MonoMac-6 cells by flow cytometry. The antitubercular effect was characterized by the enumeration of colony-forming units on Mycobacterium tuberculosis H37Rv infected MonoMac-6 cultures. We found that SUVmixed + TB515 has the best long-term stability. TB515 has much higher EE in both types of SUVs. Cellular uptake for native TB501 is extremely low, but if it is encapsulated in SUVmixed it appreciably increases; in the case of TB515, quasi total uptake is accessible. It is concluded that SUVmixed + TB501 seems to be the most efficacious antitubercular formulation given the presented experiments; to find the most promising antituberculotic formulation for therapy further in vivo investigations are needed.
The photodynamic effect requires the simultaneous presence of light, photosensitizer (PS) and molecular oxygen. In this process, the photoinduced damage of cells is caused by reactive oxygen species (ROS). Besides DNA, the other target of ROS is the membranes, separating internal compartments in living cells. Hence, the ability of ROS formation of porphyrins as PSs, in liposomes as simple models of cellular membranes is of outstanding interest. Earlier we compared the binding parameters and locations of mesoporphyrin IX dihydrochloride (MPCl) and mesoporphyrin IX dimethyl ester (MPE), in small unilamellar vesicles (SUV) made from various saturated phosphatidylcholines. In this study, we used the same kinds of samples for comparing the ROS forming ability. Triiodide production from potassium iodide because of light-induced ROS in the presence of molybdate catalyst was applied, and the amount of product was quantitatively followed by optical spectrometry. Furthermore, we demonstrated and carefully studied SUVs disruption as direct evidence of membrane destruction by the methods of dynamic light scattering (DLS) and fluorescence correlation spectroscopy (FCS), applying unsaturated phosphatidylcholines as membrane components. Although the ROS forming ability is more pronounced in the case of MPCl, we found that the measured disruption was more effective in the samples containing MPE.
OMPs to form outer membrane (OM) islands. Super-resolution imaging, i.e. stochastic optical reconstruction microscopy (STORM) and structured illumination microscopy (SIM), has been used to reveal the size and surface distribution of colicin-receptor complexes in these OM islands. Using confocal fluorescence recovery after photo-bleaching (FRAP) microscopy, we have for the first time detected in vivo assembly of the translocon complex observed as tethering of the inner membrane protein TolA by the N-terminus of ColE9 in a BtuB and TolB dependent manner. These in vivo studies have demonstrated that delivery of the intrinsically unstructured N-terminus of ColE9 to the periplasm is sufficient to assemble a periplasm-spanning translocon complex and that this occurs while the colicin molecule remains receptor-bound at the extracellular surface. Work is underway to elucidate the role of trans-periplasmic energy transduction in the formation and maintenance of this translocon complex.
membrane-spanning bipolar macrocycles that may allow the organisms to maintain the large pH gradient they require to survive. We investigated the relationship between the chemical structure of a number of lipids and the proton permeability of the membranes they form by using an optimized proton permeation assay performed on liposomes containing a fluorescent indicator dye. This work focuses on the effects of tethering on proton permeability and examines lipids with membrane-spanning chains of varied length and chemical structure (e.g. number and identity of rings). We discuss the results in the context of similar chemical groups and structures found in the cell membranes of extremophiles.
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