Fluorescent probes are powerful tools for the investigations of reactive oxygen species (ROS) in living organisms by visualization and imaging. However, the multiparallel assays of several ROS with multiple probes are often limited by the available number of spectrally nonoverlapping chromophores together with large invasive effects and discrepant biological locations. Meanwhile, the spontaneous ROS profilings in various living organs/tissues are also limited by the penetration capability of probes across different biological barriers and the stability in reactive in vivo environments. Here, we report a single fluorescent probe to achieve the effective discrimination and profiling of hydroxyl radicals (•OH) and hypochlorous acid (HClO) in living organisms. The probe is constructed by chemically grafting an additional five-membered heterocyclic ring and a lateral triethylene glycol chain to a fluorescein mother, which does not only turn off the fluorescence of fluorescein, but also create the dual reactive sites to ROS and the penetration capability in passing through various biological barriers. The reactions of probe with •OH and HClO simultaneously result in cyan and green emissions, respectively, providing the real-time discrimination and quantitative analysis of the two ROS in cellular mitochondria. Surprisingly, the accumulation of probes in the intestine and liver of a normal-state zebrafish and the transfer pathway from intestine-to-blood-to-organ/tissue-to-kidney-to-excretion clearly present the profiling of spontaneous •OH and HClO in these metabolic organs. In particular, the stress generation of •OH at the fresh wound of zebrafish is successfully visualized for the first time, in spite of its extremely short lifetime.

The dynamics of DNAa nd RNAs tructures in live cells are important for understanding cell behaviors,s uch as transcription activity,p rotein expression, cell apoptosis,a nd hereditary disease,b ut are challenging to monitor in live organisms in real time.The difficulty is largely due to the lack of photostable imaging probes that can distinguish between DNAand RNA, and more importantly,are capable of crossing multiple membrane barriers ranging from the cell/organelle to the tissue/organ level. We report the discovery of ac ationic carbon quantum dot (cQD) probe that emits spectrally distinguishable fluorescence upon binding with doublestranded DNAa nd single-stranded RNAi nl ive cells,t hereby enabling real-time monitoring of DNAand RNAl ocalization and motion. Asurprising finding is that the probe can penetrate through various types of biological barriers in vitro and in vivo.Combined with standardand super-resolution microscopy, photostable cQDs allowtime-lapse imaging of chromatin and nucleoli during cell division and Caenorhabditis elegans (C.elegans) growth.

Objective. Learning the structures and unknown correlations of a motor imagery electroencephalogram (MI-EEG) signal is important for its classification. It is also a major challenge to obtain good classification accuracy from the increased number of classes and increased variability from different people. In this study, a four-class MI task is investigated. Approach. An end-to-end novel hybrid deep learning scheme is developed to decode the MI task from EEG data. The proposed algorithm consists of two parts: a. A one-versus-rest filter bank common spatial pattern is adopted to preprocess and pre-extract the features of the four-class MI signal. b. A hybrid deep network based on the convolutional neural network and long-term short-term memory network is proposed to extract and learn the spatial and temporal features of the MI signal simultaneously. Main results. The main contribution of this paper is to propose a hybrid deep network framework to improve the classification accuracy of the four-class MI-EEG signal. The hybrid deep network is a subject-independent shared neural network, which means it can be trained by using the training data from all subjects to form one model. Significance. The classification performance obtained by the proposed algorithm on brain–computer interface (BCI) competition IV dataset 2a in terms of accuracy is 83% and Cohen’s kappa value is 0.80. Finally, the shared hybrid deep network is evaluated by every subject respectively, and the experimental results illustrate that the shared neural network has satisfactory accuracy. Thus, the proposed algorithm could be of great interest for real-life BCIs.

Fluorescent colorimetry test papers are promising for the assays of environments, medicines, and foods by the observation of the naked eye on the variations of fluorescence brightness and color. Unlike dye-absorption-based pH test paper, however, the fluorescent test papers with wide color-emissive variations with target dosages for accurate quantification remain unsuccessful even if the multicolorful fluorescent probes are used. Here, we report the dosage-sensitive fluorescent colorimetry test paper with a very wide/consecutive "from red to cyan" response to the presence and amount of arsenic ions, As(III). Red quantum dots (QDs) were modified with glutathione and dithiothreitol to obtain the supersensitivity to As(III) by the quenching of red fluorescence through the formation of dispersive QDs aggregates. A small amount of cyan carbon dots (CDs) with spectral blue-green components as the photostable internal standard were mixed into the QDs solution to produce a composited red fluorescence. Upon the addition of As(III) into the sensory solution, the fluorescence color could gradually be reversed from red to cyan with a detection limit of 1.7 ppb As(III). When the sensory solution was printed onto a piece of filter paper, surprisingly a serial of color evolution from peach to pink to orange to khaki to yellowish to yellow-green to final cyan with the addition of As(III) was displayed and clearly discerned the dosage scale as low as 5 ppb. The methodology reported here opens a novel pathway toward the real applications of fluorescent test papers.

Graphene oxide has widely been employed in various fields, but its structure and composition has still not been fully understood. Here we report that freshly prepared graphene oxide exhibits a large number of π-conjugated carbon radicals at its π-network plane, which result from the addition reaction of hydroxyl radicals from H2O2 onto the conjugated double bonds of graphene oxide. The π-conjugated carbon radicals can directly initiate the long-lasting visible chemiluminescence of luminol, which is even stronger than that obtained when horseradish peroxidase and H2O2 are used. Previously, graphene oxide was mainly reported to be a quencher of chemiluminescence instead. Remarkably, the reacted radicals can be regenerated, thereby enabling the repetitive initiation of chemiluminescence by re-treatment of graphene oxide. The results reported here provide a new understanding of the structure, properties, and applications of graphene oxide.

Intracellular lipid metabolism occurs in lipid droplets (LDs), which is critical to the survival of cells. Imaging LDs is an intuitive way to understand their physiology in live cells. However, this is limited by the availability of specific probes that can properly visualize LDs in vivo. Here, an LDs-specific red-emitting probe is proposed to address this need, which is not merely with an ultrahigh signal-to-noise (S/N) ratio and a large Stokes shift (up to 214 nm) but also with superior resistance to photobleaching. The probe has been successfully applied to real-time tracking of intracellular LDs behaviors, including fusion, migration, and lipophagy processes. We deem that the proposed probe here offers a new possibility for deeper understanding of LDs-associated behaviors, elucidation of their roles and mechanisms in cellular metabolism, and determination of the transition between adaptive lipid storage and lipotoxicity as well.

Visualizing and dynamic tracking lipid droplets (LDs) are of great importance to biological research. Herein, two-photon absorption fluorescent small bioprobes based on lipophilic coumarin were developed, which exhibited high selectivity toward LDs in HeLa cells. Because of good biocompatibility and excellent photostability, the probes were applied to realize specific super-resolution visualization of the intracellular LDs in HeLa cells, offering us the quantitative results of the amount and diameters of LDs as well. Furthermore, the bioprobes were capable of monitoring the movements of the LDs in real time. We believe that bioprobes would provide new avenues to designing bioimaging and biological diagnosis.

Previous studies have reported that a dawn enhancement does not present in the statistical picture of the equatorial ionospheric vertical plasma drift, while it clearly shows in case measurements. In this statistical study, it is the first time to investigate the occurrence of the dawn enhancement in the equatorial ionospheric vertical plasma drift from ROCSAT‐1 observations during geomagnetic quiet times. The dawn enhancements occur most frequently in June solstice and least frequently in December solstice. The statistical survey shows that the occurrence depends on the magnetic declination. The enhancement has the strongest amplitude in regions near 320° longitude and peaks during June solstice. The dawn enhancement reaches its peak after the sunrise in conjugated E regions. Furthermore, it is found that the dawn enhancement is closely related to the difference between the sunrise times in the conjugated E regions (sunrise time lag). The dawn enhancement occurs easily in regions with a large sunrise time lag.