Michael Ming-tak Loy

Oxygen‐Assisted Charge Transfer Between ZnO Quantum Dots and Graphene

Efficient charge transfer between ZnO quantum dots (QDs) and graphene is demonstrated by decorating ZnO QDs on top of graphene, with the assistance of oxygen molecules from the air. The electrical response of the device to UV light is greatly enhanced, and a photoconductive gain of up to 10(7) can be obtained.

A Mitochondrion-Specific Photoactivatable Fluorescence Turn-On AIE-Based Bioprobe for Localization Super-Resolution Microscope

A novel mitochondrion-specific photo-activatable fluorescence turn-on bioprobe, named as o-TPE-ON+, is designed and readily prepared, operating through a new photoactivatable mechanism of photocyclodehydrogenation. This bioprobe exhibits unique photoactivation behavior in cells, and is applied to super-resolution imaging of mitochondrion and its dynamic investigation in both fixed and live cells under physiological conditions without any external additives.

Photon Pairs With Coherence Time Exceeding 1 μs

The generation of nonclassical photon pairs with a long coherence time is key for applications that range from fundamental to quantum communication and metrology. Spontaneous four-wave mixing with electromagnetically induced transparency has been demonstrated as one of the most efficient methods; however, narrowing the bandwidth and producing photon pairs with a temporal length beyond 1xa0μs remains a technical challenge due to noise considerations and the need for cold atoms with a high optical depth (OD). In this work, we demonstrate the generation of narrowband photon pairs with a controllable coherence time up to 1.72xa0μs in a laser-cooled atomic ensemble with an OD as high as 130. At such a high OD, we find that the pump laser field spatial profile has a significant effect on the time–frequency entangled two-photon waveform. We also confirm the quantum particle nature of heralded narrowband single photons generated from this source.

Subnatural-linewidth Biphotons from a Doppler-broadened Hot Atomic Vapour Cell

Entangled photon pairs, termed as biphotons, have been the benchmark tool for experimental quantum optics. The quantum-network protocols based on photon–atom interfaces have stimulated a great demand for single photons with bandwidth comparable to or narrower than the atomic natural linewidth. In the past decade, laser-cooled atoms have often been used for producing such biphotons, but the apparatus is too large and complicated for engineering. Here we report the generation of subnatural-linewidth (<6u2009MHz) biphotons from a Doppler-broadened (530u2009MHz) hot atomic vapour cell. We use on-resonance spontaneous four-wave mixing in a hot paraffin-coated 87Rb vapour cell at 63u2009°C to produce biphotons with controllable bandwidth (1.9–3.2u2009MHz) and coherence time (47–94u2009ns). Our backward phase-matching scheme with spatially separated optical pumping is the key to suppress uncorrelated photons from resonance fluorescence. The result may lead towards miniature narrowband biphoton sources.

Measuring the biphoton temporal wave function with polarization-dependent and time-resolved two-photon interference.

We describe and demonstrate a quantum state tomography for measuring the complex temporal waveform of narrowband biphotons. Through six sets of two-photon interference measurements projected in different polarization subspaces, we can construct the time-frequency entangled twophoton joint amplitude and phase functions in continuous-variable time domain. For the first time, we apply this technique to experimentally determine the temporal quantum states of narrowband biphotons generated from spontaneous four-wave mixing in cold atoms, and fully confirm the theoretical predictions.

A Distinct Pathway for Polar Exocytosis in Plant Cell Wall Formation.

A distinct Golgi-derived polar exocytosis pathway occurs in Nicotiana tabacum for pectin methylesterase 1 and contributes to cell wall and cell plate formation during cytokinesis. Post-Golgi protein sorting and trafficking to the plasma membrane (PM) is generally believed to occur via the trans-Golgi network (TGN). In this study using Nicotiana tabacum pectin methylesterase (NtPPME1) as a marker, we have identified a TGN-independent polar exocytosis pathway that mediates cell wall formation during cell expansion and cytokinesis. Confocal immunofluorescence and immunogold electron microscopy studies demonstrated that Golgi-derived secretory vesicles (GDSVs) labeled by NtPPME1-GFP are distinct from those organelles belonging to the conventional post-Golgi exocytosis pathway. In addition, pharmaceutical treatments, superresolution imaging, and dynamic studies suggest that NtPPME1 follows a polar exocytic process from Golgi-GDSV-PM/cell plate (CP), which is distinct from the conventional Golgi-TGN-PM/CP secretion pathway. Further studies show that ROP1 regulates this specific polar exocytic pathway. Taken together, we have demonstrated an alternative TGN-independent Golgi-to-PM polar exocytic route, which mediates secretion of NtPPME1 for cell wall formation during cell expansion and cytokinesis and is ROP1-dependent.

Shaping the Biphoton Temporal Waveform with Spatial Light Modulation

We demonstrate a technique for shaping the temporal wave function of biphotons generated from spatially modulated spontaneous four-wave mixing in cold atoms. We show that the spatial profile of the pump field can be mapped onto the biphoton temporal wave function in the group delay regime. The spatial profile of the pump laser beam is shaped by using a spatial light modulator. This spatial-to-temporal mapping enables the generation of narrow-band biphotons with controllable temporal waveforms.

A user-friendly two-color super-resolution localization microscope.

We report a robust two-color method for super-resolution localization microscopy. Two-dye combination of Alexa647 and Alexa750 in an imaging buffer containing COT and using TCEP as switching regent provides matched and balanced switching characteristics for both dyes, allowing simultaneous capture of both on a single camera. Active sample locking stabilizes sample with 1nm accuracy during imaging. With over 4,000 photons emitted from both dyes, two-color superresolution images with high-quality were obtained in a wide range of samples including cell cultures, tissue sections and yeast cells.

Multicolor 4D Fluorescence Microscopy using Ultrathin Bessel Light Sheets

We demonstrate a simple and efficient method for producing ultrathin Bessel (‘non-diffracting’) light sheets of any color using a line-shaped beam and an annulus filter. With this robust and cost-effective technology, we obtained two-color, 3D images of biological samples with lateral/axial resolution of 250u2009nm/400u2009nm, and high-speed, 4D volume imaging of 20u2009μm sized live sample at 1u2009Hz temporal resolution.

ATM protein is located on presynaptic vesicles and its deficit leads to failures in synaptic plasticity

Ataxia telangiectasia is a multisystemic disorder that includes a devastating neurodegeneration phenotype. The ATM (ataxia-telangiectasia mutated) protein is well-known for its role in the DNA damage response, yet ATM is also found in association with cytoplasmic vesicular structures: endosomes and lysosomes, as well as neuronal synaptic vesicles. In keeping with this latter association, electrical stimulation of the Schaffer collateral pathway in hippocampal slices from ATM-deficient mice does not elicit normal long-term potentiation (LTP). The current study was undertaken to assess the nature of this deficit. Theta burst-induced LTP was reduced in Atm(-/-) animals, with the reduction most pronounced at burst stimuli that included 6 or greater trains. To assess whether the deficit was associated with a pre- or postsynaptic failure, we analyzed paired-pulse facilitation and found that it too was significantly reduced in Atm(-/-) mice. This indicates a deficit in presynaptic function. As further evidence that these synaptic effects of ATM deficiency were presynaptic, we used stochastic optical reconstruction microscopy. Three-dimensional reconstruction revealed that ATM is significantly more closely associated with Piccolo (a presynaptic marker) than with Homer1 (a postsynaptic marker). These results underline how, in addition to its nuclear functions, ATM plays an important functional role in the neuronal synapse where it participates in the regulation of presynaptic vesicle physiology.