Common pathways for growth and for plasticity. Curr Opin Neurobiol 22, 405-411, doi:10.1016/j.conb.2012.02.008 (2012)
Phospholipases C and sphingomyelinases: Lipids as substrates and modulators of enzyme activity. Prog Lipid Res 51, 238–266 (2012).
Lipid bilayers in the gel phase become saturated by Triton X-100 at lower surfactant concentrations than those in the fluid phase. Biophys. J. 102 1–7 (2012).
Mechanistic insights into the retaining glucosyl-3-phosphoglycerate synthase from mycobacteria. J Biol. Chem. 287, 24649-24661 (2012).
Binding of b-Amyloid (1–42) peptide to negatively charged phospholipid membranes in the liquid-ordered state: modeling and experimental studies. Biophys. J. 103, 453–463 (2012).
The effect of amyloidogenic peptides on bacterial aging correlates with their intrinsic aggregation propensity. J. Mol. Biol. 421, 270-281 (2012).
Pores of the toxin FraC assemble into 2D hexagonal clusters in both crystal structures and model membranes. J. Struct. Biol. 180, 312-317 (2012).
Deletion of a single helix from the transmembrane domain causes large changes in membrane insertion properties and secondary structure of the bacterial conjugation protein TrwB Biochim Biophys Acta. 1818, 3158-3166 (2012).
Siglec-1 is a novel dendritic cell receptor that mediates HIV-1 trans-infection through recognition of viral membrane gangliosides. PLoS Biol. 10(12):e1001448. doi: 10.1371/journal.pbio.1001448 (2012).
Insights into sphingolipid miscibility: separate observation of sphingomyelin and ceramide N-acyl chain melting. Biophys J. 103, 2465-2474 (2012).