Residue specific partitioning of KL4 into phospholipid bilayers.

KL4, which has demonstrated success in the treatment of respiratory distress, is a synthetic helical, amphipathic peptide mimetic of lung surfactant protein B. The unusual periodicity of charged residues within KL4 and its relatively high hydrophobicity distinguish it from canonical amphipathic helical peptides. Here we utilized site specific spin labeling of both lipids and the peptide coupled with EPR spectroscopy to discern the effects of KL4 on lipid dynamics, the residue specific dynamics of hydrophobic regions within KL4, and the partitioning depths of specific KL4 residues into the DPPC/POPG and POPC/POPG lipid bilayers under physiologically relevant conditions. KL4 induces alterations in acyl chain dynamics in a lipid-dependent manner, with the peptide partitioning more deeply into DPPC-rich bilayers. Combined with an earlier NMR study of changes in lipid dynamics on addition of KL4 (V.C. Antharam et al., 2009), we are able to distinguish how KL4 affects both collective bilayer motions and intramolecular acyl chain dynamics in a lipid-dependent manner. EPR power saturation results for spin labeled lipids demonstrate that KL4 also alters the accessibility profiles of paramagnetic colliders in a lipid-dependent manner. Measurements of dynamics and depth parameters for individual spin-labeled residues within KL4 are consistent with a model where the peptide partitions deeply into the lipid bilayers but lies parallel to the bilayer interface in both lipid environments; the depth of partitioning is dependent on the degree of lipid acyl chain saturation within the bilayer.

Template synthesis of gold nanotubes in an anodic alumina membrane.

Nanotube-containing membranes prepared by the template method show promise for use as highly selective filters for membrane-based chemical and biological separations. Most of the work to date has been done on gold nanotubes prepared by electroless deposition of Au within the pores of polymeric filtration membranes. These polymeric filters have very low porosities (< 1%), and, as a result, the flux through Au nanotube membranes based on these templates is very low. In contrast, the other popular template membranes-anodic aluminas-have high porosities-30% to 50%. In spite of this potential advantage of anodic alumina templates, there have been no reports of electrolessly plated Au nanotubes within the pores of these templates. This is because the electroless plating method used to deposit Au nanotubes in polymeric templates does not work in aluminas. We have developed a modified electroless plating strategy that can be used to deposit high-quality Au nanotubes within the pores of the alumina templates. We describe this new plating method here.