Nanopatterning by molecular self-assembly on surfaces.

The ability to pattern surfaces down to the nanoscale is of increasing importance in nanoscience research. The use of supramolecular chemistry to drive the formation of self-assembled networks allows for a bottom-up approach to achieve nanopatterned surfaces. This short review highlights some of the recent breakthroughs in achieving long-range order in such molecular based systems, complemented with examples from our own work. The tuning of molecular architectures can exert control on the emergent properties and function of molecules at interfaces. In particular the formation of porous honeycomb networks allows the rational design of highly ordered patterned surface domains and the investigation of molecular dynamics, chirality and templating effects on surfaces.

Presynaptic induction and expression of timing-dependent long-term depression demonstrated by compartment-specific photorelease of a use-dependent NMDA receptor antagonist.

NMDA receptors are important for synaptic plasticity, including long-term potentiation (LTP) and long-term depression (LTD). To help investigate the precise location of the NMDA receptors that are required for different types of synaptic plasticity, we synthesized a caged form of the use-dependent NMDA receptor antagonist MK801, which we loaded into individual neurons in vitro, followed by compartment-specific uncaging. We used this method to investigate timing-dependent plasticity at layer 4-layer 2/3 synapses of mouse barrel cortex. Somatodendritic photorelease of MK801 in the postsynaptic neuron produced a use-dependent block of synaptic NMDA receptor-mediated currents and prevented the induction of LTP. Compartment-specific photorelease of MK801 in the presynaptic neuron showed that axonal, but not somatodendritic, presynaptic NMDA receptors are required for induction of LTD. The rate of use-dependent block of postsynaptic NMDA receptor current was slower following induction of LTD, consistent with a presynaptic locus of expression. Thus, this new caged compound has demonstrated the axonal location of NMDA receptors required for induction and the presynaptic locus of expression of LTD at layer 4-layer 2/3 synapses.