AI Article Synopsis

  • Researchers created mixed monolayers using distearoylphosphatidylcholine (DSPC) and PEG-grafted phospholipids to model bio-non-fouling surfaces and investigate their properties.
  • They employed epifluorescence microscopy to visualize the distribution of PEG molecules within the DSPC matrix, analyzing fluorescence from a tagged fluorescein.
  • The study found that DSPE-PEG2000 mixed nonideally with DSPC, transitioning from phase separation to homogeneity under increased surface pressure and PEG content, influenced by interactions and chain tilt mismatches.

Article Abstract

Mixed monolayers of distearoylphosphatidylcholine (DSPC) and a poly(ethylene glycol)-(PEG)-grafted distearoylphosphatidylethanolamine with a PEG molecular weight of 2000, DSPE-PEG2000, spread on phosphate-buffered saline (PBS) were used as models of bio-non-fouling membrane-mimetic surfaces in order to visualize the lateral distribution of PEG2000-phospholipid in the host phospholipid matrix. Epifluorescence microscopy (EFM) was used to locate DSPE-PEG2000 molecules in the DSPC matrix by detecting the fluorescence from a fluorescein fluorophore attached to the distal end of the PEG2000 chain. Comparative analysis of surface pressure-area isotherms and EFM images revealed that DSPE-PEG2000 mixes nonideally with DSPC in monolayers on a PBS subphase. A transition from a phase-separated monolayer to a homogeneous mixture was observed with increasing surface pressure and PEG content. The effect of nonideal mixing behavior of DSPE-PEG2000 on its lateral distribution in the DSPC matrix was interpreted in terms of excluded volume interactions between the PEG2000 chains and a mismatch in the tilt of aliphatic chains on DSPC and DSPE-PEG2000 molecules.

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Source
http://dx.doi.org/10.1021/la802205yDOI Listing

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