Measurement of replication structures at the nanometer scale using super-resolution light microscopy.

DNA replication, similar to other cellular processes, occurs within dynamic macromolecular structures. Any comprehensive understanding ultimately requires quantitative data to establish and test models of genome duplication. We used two different super-resolution light microscopy techniques to directly measure and compare the size and numbers of replication foci in mammalian cells.

Mechanisms of polarization switching in single-transverse-mode vertical-cavity surface-emitting lasers: thermal shift and nonlinear semiconductor dynamics.

We analyze polarization switching in vertical-cavity surface-emitting lasers, taking into account a proper semiconductor frequency-dependent complex susceptibility and spin-flip processes. Thermal effects are included as a varying detuning, and gain differences arise from birefringence splitting. We find that, for large birefringence, gain differences between the two linearly polarized modes are preponderant, and switching occurs owing to thermal shift.

Targeting and tracing antigens in live cells with fluorescent nanobodies.

We fused the epitope-recognizing fragment of heavy-chain antibodies from Camelidae sp. with fluorescent proteins to generate fluorescent, antigen-binding nanobodies (chromobodies) that can be expressed in living cells. We demonstrate that chromobodies can recognize and trace antigens in different subcellular compartments throughout S phase and mitosis.