AI Article Synopsis

  • The study investigates how human serum albumin (HSA) and DPPC mixed monolayers behave when spread on water at 25°C, using advanced techniques to analyze their characteristics.
  • The presence of two phase transitions in the mixed monolayers was identified through isotherm data and compressional modulus curves, indicating complex interactions between HSA and DPPC.
  • Measurements show that at certain surface pressures, HSA is partially excluded from the interface, resulting in a predominance of DPPC domains, though some HSA remains in a specific packing arrangement, as observed in microscopy images.

Article Abstract

The aim of this study is to deepen the understanding of the behavior of human serum albumin (HSA) and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) mixed monolayers. For this purpose, different amounts of DPPC were spread at 25°C on the water surface containing a monolayer of HSA. Surface film balance and Brewster angle microscopy techniques have been used to analyze the structural and energetic characteristics (structure, topography, thickness, miscibility and interactions) of these mixtures. HSA/DPPC mixed monolayers exhibit two phase transitions evidenced by two discontinuities in the corresponding π-A isotherms and by two minimum values in the compressional modulus (C(s)(-1))-surface pressure (π) curves. The plot of the molecular areas occupied by the mixed monolayers as function of the mass fraction of DPPC shows the absence of deviations from linearity, a typical behavior for ideal or inmiscible system. This result was confirmed from the values calculated for the free energy of excess (ΔG(exc)), which are practically zero whatever the composition of the mixtures and the surface pressures at which ΔG(exc) values were calculated. In addition, relative thickness values of HSA/DPPC mixed monolayers showed the existence of an exclusion surface pressure (π(exc)), below which the monolayer is composed of a mixture of both components, while above π(exc) the HSA molecules are squeezed out the interface, but not totally. In fact, although in this region DPPC domains predominate at the interface, the existence of protein molecules in a packing "loops" configuration can be observed in BAM images. Moreover, relative thickness measurements confirm this hypothesis.

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Source
http://dx.doi.org/10.1016/j.colsurfb.2011.11.022DOI Listing

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