204 research outputs found
MINSTED fluorescence localization and nanoscopy
We introduce MINSTED, a fluorophore localization and super-resolution microscopy concept based on stimulated emission depletion (STED) that provides spatial precision and resolution down to the molecular scale. In MINSTED, the intensity minimum of the STED doughnut, and hence the point of minimal STED, serves as a movable reference coordinate for fluorophore localization. As the STED rate, the background and the required number of fluorescence detections are low compared with most other STED microscopy and localization methods, MINSTED entails substantially less fluorophore bleaching. In our implementation, 200–1,000 detections per fluorophore provide a localization precision of 1–3 nm in standard deviation, which in conjunction with independent single fluorophore switching translates to a ~100-fold improvement in far-field microscopy resolution over the diffraction limit. The performance of MINSTED nanoscopy is demonstrated by imaging the distribution of Mic60 proteins in the mitochondrial inner membrane of human cells
Instability driven fragmentation of nanoscale fractal islands
Formation and evolution of fragmentation instabilities in fractal islands,
obtained by deposition of silver clusters on graphite, are studied. The
fragmentation dynamics and subsequent relaxation to the equilibrium shapes are
controlled by the deposition conditions and cluster composition. Sharing common
features with other materials' breakup phenomena, the fragmentation instability
is governed by the length-to-width ratio of the fractal arms.Comment: 5 pages, 3 figures, Physical Review Letters in pres
Mapping protein interactions in the active TOM-TIM23 supercomplex
Nuclear-encoded mitochondrial proteins destined for the matrix have to be transported across two membranes. The TOM and TIM23 complexes facilitate the transport of precursor proteins with N-terminal targeting signals into the matrix. During transport, precursors are recognized by the TIM23 complex in the inner membrane for handover from the TOM complex. However, we have little knowledge on the organization of the TOM-TIM23 transition zone and on how precursor transfer between the translocases occurs. Here, we have designed a precursor protein that is stalled during matrix transport in a TOM-TIM23-spanning manner and enables purification of the translocation intermediate. Combining chemical cross-linking with mass spectrometric analyses and structural modeling allows us to map the molecular environment of the intermembrane space interface of TOM and TIM23 as well as the import motor interactions with amino acid resolution. Our analyses provide a framework for understanding presequence handover and translocation during matrix protein transport
Electromigration-Induced Flow of Islands and Voids on the Cu(001) Surface
Electromigration-induced flow of islands and voids on the Cu(001) surface is
studied at the atomic scale. The basic drift mechanisms are identified using a
complete set of energy barriers for adatom hopping on the Cu(001) surface,
combined with kinetic Monte Carlo simulations. The energy barriers are
calculated by the embedded atom method, and parameterized using a simple model.
The dependence of the flow on the temperature, the size of the clusters, and
the strength of the applied field is obtained. For both islands and voids it is
found that edge diffusion is the dominant mass-transport mechanism. The rate
limiting steps are identified. For both islands and voids they involve
detachment of atoms from corners into the adjacent edge. The energy barriers
for these moves are found to be in good agreement with the activation energy
for island/void drift obtained from Arrhenius analysis of the simulation
results. The relevance of the results to other FCC(001) metal surfaces and
their experimental implications are discussed.Comment: 9 pages, 13 ps figure
Electromigration of Single-Layer Clusters
Single-layer atom or vacancy clusters in the presence of electromigration are
studied theoretically assuming an isotropic medium. A variety of distinctive
behaviors distinguish the response in the three standard limiting cases of
periphery diffusion (PD), terrace diffusion (TD), and evaporation-condensation
(EC). A general model provides power laws describing the size dependence of the
drift velocity in these limits, consistent with established results in the case
of PD. The validity of the widely used quasistatic limit is calculated. Atom
and vacancy clusters drift in opposite directions in the PD limit but in the
same direction otherwise. In absence of PD, linear stability analysis reveals a
new type of morphological instability, not leading to island break-down. For
strong electromigration, Monte Carlo simulations show that clusters then
destabilize into slits, in contrast to splitting in the PD limit.
Electromigration affects the diffusion coefficient of the cluster and
morphological fluctuations, the latter diverging at the instability threshold.
An instrinsic attachment-detachment bias displays the same scaling signature as
PD in the drift velocity.Comment: 11 pages, 4 figure
Synthesis of Aqueous CdTe/CdS/ZnS Core/shell/shell Quantum Dots by a Chemical Aerosol Flow Method
This work described a continuous method to synthesize CdTe/CdS/ZnS core/shell/shell quantum dots. In an integrated system by flawlessly combining the chemical aerosol flow system working at high temperature (200–300°C) to generate CdTe/CdS intermediate products and an additional heat-up setup at relatively low temperature to overcoat the ZnS shells, the CdTe/CdS/ZnS multishell structures were realized. The as-synthesized CdTe/CdS/ZnS core/shell/shell quantum dots are characterized by photoluminescence spectra, X-ray diffraction (XRD), energy-dispersive X-ray spectra (EDS), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM). Fluorescence and XRD results confirm that the obtained quantum dots have a core/shell/shell structure. It shows the highest quantum yield above 45% when compared to the rhodamine 6G. The core/shell/shell QDs were more stable via the oxidation experiment by H2O2
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