Lipid phase influences the binding of Bacillus thuringiensis Cyt2Aa2 toxin on model lipid membranes

2019 ◽  
Vol 511 (2) ◽  
pp. 409-415 ◽  
Author(s):  
Sudarat Tharad ◽  
Boonhiang Promdonkoy ◽  
José L. Toca-Herrera
2020 ◽  
Author(s):  
Nanqin Mei ◽  
Morgan Robinson ◽  
James H. Davis ◽  
Zoya Leonenko

ABSTRACTThe structure and biophysical properties of lipid biomembranes are important for normal function of plasma and organelle membranes, which is essential for proper functioning of living cells. In Alzheimer’s disease (AD) the structure of neuronal membranes becomes compromised by the toxic effect of amyloid-β (Aβ) protein which accumulates at neuron synapses, resulting in membrane perforation and dysfunction, oxidative stress and cell death. Melatonin is an important pineal gland hormone that has been shown to be protective against Aβ toxicity in cellular and animal studies, but the molecular mechanism of this protection is not well understood. It has been shown that melatonin can interact with model lipid membranes and alter the membrane biophysical properties, such as membrane molecular order and dynamics. This effect of melatonin has been previously studied in simple model bilayers with one or two lipid components, we consider a more complex ternary lipid mixture as our membrane model. In this study, we used 2H-NMR to investigate the effect of melatonin on lipid phase behaviour of a three-component model lipid membranes composed of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) and cholesterol. We used deuterium labelled palmitoyl-d31 in POPC-d31 and DPPC-d62 separately, to probe the changes in hydrocarbon chain order as a function of temperature and varying concentrations of melatonin. We found that melatonin concentration influences phase separation in these ternary mixtures somewhat differently depending on whether POPC-d31 or DPPC-d62was used. At 5 mol% melatonin we observed phase separation in samples with POPC-d31, but not with DPPC-d62. However, at 10 mol% melatonin phase separation was observed in both samples with either POPC-d31 or DPPC-d62. These results indicate that melatonin can have a strong effect on membrane structure and physical properties, which may provide some clues to understanding how melatonin protects against Aβ.SIGNIFICANCEMelatonin has been shown to be protective against Aβ pathology in animal and cellular studies. Although the mechanism of this protection is not well-understood, melatonin’s membrane-active properties may be important in this regard. In this work solid-state deuterium nuclear magnetic resonance was used to study the effect of melatonin on the POPC/DPPC/cholesterol model membranes. Specifically, we showed that melatonin modifies lipid hydrocarbon chain order to promote phase separation. This knowledge helps to explain the role of melatonin in lipid domain formation and may provide a deeper understanding of the mechanism of melatonin neuroprotection in AD.


2000 ◽  
Vol 55 (9-10) ◽  
pp. 764-769
Author(s):  
Halina Kleszczyńska ◽  
Krzysztof Bielecki ◽  
Janusz Sarapuk ◽  
Anna Dziamska ◽  
Stanislaw Przestalski

Abstract The physiological and hemolytic toxicities of triphenyllead chloride (TPhL) as well as its modyfying influence on model lipid membranes were studied. The experiments allowed the determination of TPhL concentrations causing 50% inhibition of growth of Spirodela oligorrhiza, Lemna minor and Solvinia natans (EC50), 100% hemolysis of pig erythrocytes (C100) and destabilization of planar lipid membranes (CC). Also, fluidity of erythrocyte ghosts was measured by fluorescence technique and osmotic sensitivity of erythrocytes to the presence of TPhL. All parameters studied were found to be dependent on pH, of experimental solutions and the concentration of TPhL. Acidic conditions increased EC50, C100 and CC concentrations of TPhL. Fluorescence and osmotic measurements showed that osmotic stability and fluidity decreased with increasing trimethyllead concentration. A possible mechanism of TPhL toxicity is discussed. It is assumed that TPhL is interacting with the lipid phase of the models used. It is also assumed that there may exist various, ionic and nonionic, forms of TPhL as a result of its speciation under different experimental conditions. These species, due to their differentiated lipophilicity, may exert different effects on the model membranes studied.


2000 ◽  
Vol 346 (1) ◽  
pp. 223-232 ◽  
Author(s):  
Petra MALOVRH ◽  
Ariana BARLIĆ ◽  
Zdravko PODLESEK ◽  
Peter MAĆEK ◽  
Gianfranco MENESTRINA ◽  
...  

Equinatoxin II (EqtII) is a eukaryotic cytolytic toxin that avidly creates pores in natural and model lipid membranes. It contains five tryptophan residues in three different regions of the molecule. In order to study its interaction with the lipid membranes, three tryptophan mutants, EqtII Trp45, EqtII Trp116/117 and EqtII Trp149, were prepared in an Escherichia coli expression system [here, the tryptophan mutants are classified according to the position of the remaining tryptophan residue(s) in each mutated protein]. They all possess a single intrinsic fluorescent centre. All mutants were less haemolytically active than the wild-type, although the mechanism of erythrocyte damage was the same. EqtII Trp116/117 resembles the wild-type in terms of its secondary structure content, as determined from Fourier-transform infrared (FTIR) spectra and its fluorescent properties. Tryptophans at these two positions are buried within the hydrophobic interior of the protein, and are transferred to the lipid phase during the interaction with the lipid membrane. The secondary structure of the other two mutants, EqtII Trp45 and EqtII Trp149, was altered to a certain extent. EqtII Trp149 was the most dissimilar from the wild-type, displaying a higher content of random-coil structure. It also retained the lowest number of nitrogen-bound protons after exchange with 2H2O, which might indicate a reduced compactness of the molecule. Tryptophans in EqtII Trp45 and EqtII Trp149 were more exposed to water, and also remained as such in the membrane-bound form.


2005 ◽  
Vol 70 (5) ◽  
pp. 668-675 ◽  
Author(s):  
Monika Hereć ◽  
Halina Dziubińska ◽  
Kazimierz Trębacz ◽  
Jacek W. Morzycki ◽  
Wiesław I. Gruszecki

PLoS ONE ◽  
2013 ◽  
Vol 8 (10) ◽  
pp. e77115 ◽  
Author(s):  
Martin Loynaz Prieto ◽  
Ömer Oralkan ◽  
Butrus T. Khuri-Yakub ◽  
Merritt C. Maduke

2019 ◽  
Vol 116 (3) ◽  
pp. 369a
Author(s):  
Sharon E. Groover ◽  
Maryssa Beasley ◽  
Justin A. Legleiter

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