Max Davidson

TL;DR: Novel micromanipulation methods for producing fluid-state lipid bilayer networks of nanotubes and surface-immobilized vesicles with controlled geometry, topology, membrane composition, and interior contents are described.

TL;DR: Model studies demonstrate the application of proteomics-based analyses for bacterial species- and strain-level detection and identification and for characterization of environmentally relevant, metabolically diverse bacteria.

TL;DR: This cell-liposome fusion represents an approach to the manipulation of the cytoplasmic contents and surface properties of single cells and introduces a membrane protein reconstituted in liposomes into the cell plasma membrane.

TL;DR: This study has demonstrated that multiple methods are required to successfully analyse the membranome of a desired cell type and provides a mechanism for rapidly discovering and evaluating antibody tractable targets, which can significantly accelerate the therapeutic discovery process.

TL;DR: Nanotube-vesicle networks with reconstituted membrane protein from cells and with interior activity defined by an injection of microparticles or molecular probes are described and shown how injecting small unilamellar protein-containing vesicles can differentiate the contents of individual containers in a network.