Journal article
      
      
      
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      Monolayer properties of 1,3-diamidophospholipids
      
      
        
      
      
      
      
        
          
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Fedotenko, lllya A.
  Department of Organic Chemistry, University of Geneva, Switzerland
          
 
          
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Stefaniu, Cristina
Max Planck Institute of Colloids and Interfaces, Research Campus, Potsdam-Golm, Germany
          
 
          
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Brezesinski, Gerald
Max Planck Institute of Colloids and Interfaces, Research Campus, Potsdam-Golm, Germany
          
 
          
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Zumbuehl, Andreas
  Department of Chemistry, University of Fribourg, Switzerland
          
 
          
        
        
       
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
        
        Published in:
        
          
            
            - Langmuir. - 2013, vol. 29, no. 30, p. 9428–9435
 
            
          
         
       
      
      
      
       
      
      
      
        
        English
        
        
        
          While nature provides an endless variety of phospholipids presenting hydrolyzable ester linkages for the 1,2-positioned hydrocarbon tails, we designed and synthesized 1,3-diamidophospholipids which contain stable fatty acid amides. These new phospholipids form faceted unilamellar vesicles with mechanosensitive properties. Aiming to understand the mechanism responsible for this behavior at a molecular level, we investigated the 1,3-diamidophospholipid family in monolayers, a simplified model membrane system. Langmuir isotherms combined with in situ grazing incidence X-ray diffraction (GIXD), specular X-ray reflectivity (XR), and infrared reflection–absorption spectroscopy (IRRAS) allowed the characterization of the monolayers from a structural and thermodynamical point of view. The existence of strong headgroup interactions due to the formation of a hydrogen-bonding network was clearly revealed by IRRAS and by the high rigidity of the monolayers. GIXD showed that only the longer chain compounds of the series (Pad-PC-Pad (1,3-dipalmitamidopropan-2-phosphocholine) and Sad-PC-Sad (1,3-distearamidopropan-2-phosphocholine) were able to form ordered monolayers. The chains are strongly tilted in a rigid lattice formed due to these hydrogen-bonding interactions between the headgroups. The thermodynamical analysis leads to a critical temperature of the monolayer which is clearly different from the main phase transition temperature in bulk, indicating that there must be a different structural arrangement of the 1,3-diamidophospholipids in monolayers and in bilayers.
        
        
       
      
      
      
        
        
        
        
        
        
        
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        - Faculté des sciences et de médecine
 
        
        
        
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        - Département de Chimie
 
        
        
        
        
        
        
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                  Chemistry
                
              
            
          
        
 
        
        
        
          
        
        
        
          
        
        
        
        
        
        
        
        
        
        
        
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          https://folia.unifr.ch/unifr/documents/303235
        
 
      
     
   
  
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