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- 2019
- 7nm silicon node
- chip-package interaction
- laser assisted bonding
- quick temperature cycling test
- mass reflow
- embedded trace substrate
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- Electronic Science and Technology
- MediaTek, Inc.
- JCET STATS ChipPAC Pte. Ltd.
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Molecular recognition of the native HIV-1 MPER revealed by STED microscopy of single virions
摘要： Antibodies against the Membrane-Proximal External Region (MPER) of the Env gp41 subunit neutralize HIV-1 with exceptional breadth and potency. Due to the lack of knowledge on the MPER native structure and accessibility, different and exclusive models have been proposed for the molecular mechanism of MPER recognition by broadly neutralizing antibodies. Here, accessibility of antibodies to the native Env MPER on single virions has been addressed through STED microscopy. STED imaging of fluorescently labeled Fabs reveals a common pattern of native Env recognition for HIV-1 antibodies targeting MPER or the surface subunit gp120. In the case of anti-MPER antibodies, the process evolves with extra contribution of interactions with the viral lipid membrane to binding specificity. Our data provide biophysical insights into the recognition of the potent and broadly neutralizing MPER epitope on HIV virions, and as such is of importance for the design of therapeutic interventions.
关键词： broadly neutralizing antibodies,STED microscopy,HIV-1,Env glycoprotein,MPER
更新于2025-09-11 14:15:04
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Dynamic nanoscale morphology of the ER surveyed by STED microscopy
摘要： The endoplasmic reticulum (ER) is composed of interconnected membrane sheets and tubules. Superresolution microscopy recently revealed densely packed, rapidly moving ER tubules mistaken for sheets by conventional light microscopy, highlighting the importance of revisiting classical views of ER structure with high spatiotemporal resolution in living cells. In this study, we use live-cell stimulated emission depletion (STED) microscopy to survey the architecture of the ER at 50-nm resolution. We determine the nanoscale dimensions of ER tubules and sheets for the first time in living cells. We demonstrate that ER sheets contain highly dynamic, subdiffraction-sized holes, which we call nanoholes, that coexist with uniform sheet regions. Reticulon family members localize to curved edges of holes within sheets and are required for their formation. The luminal tether Climp63 and microtubule cytoskeleton modulate their nanoscale dynamics and organization. Thus, by providing the first quantitative analysis of ER membrane structure and dynamics at the nanoscale, our work reveals that the ER in living cells is not limited to uniform sheets and tubules; instead, we suggest the ER contains a continuum of membrane structures that includes dynamic nanoholes in sheets as well as clustered tubules.
关键词： STED microscopy,Climp63,nanoholes,endoplasmic reticulum,reticulon,microtubule cytoskeleton
更新于2025-09-10 09:29:36
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[IEEE 2018 20th International Conference on Transparent Optical Networks (ICTON) - Bucharest (2018.7.1-2018.7.5)] 2018 20th International Conference on Transparent Optical Networks (ICTON) - Pump-Probe Nanoscopy by Means of Transient Absorption Saturation
摘要： In this paper, we present a method to perform super-resolution label-free optical microscopy by means of the saturation of the transient absorption process. We developed a novel and easy-to-implement setup based on a commercial confocal microscope. We demonstrate the imaging capability by looking at single layer graphene (SLG) deposited on a glass surface via chemical vapour deposition (CVD). Exploiting near-infrared femtosecond pulsed laser beams and saturation of the transient absorption, we can reach a resolution below λ/10 nm.
关键词： absorption saturation,nanoscopy,NIR,pump-probe,STED,graphene
更新于2025-09-10 09:29:36
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Self-healing dyes for super-resolution fluorescence microscopy
摘要： In recent years, optical microscopy techniques have emerged that allow optical imaging at unprecedented resolution beyond the diffraction limit. These techniques exploit photostabilizing buffers to enable photoswitching and/or the enhancement of fluorophore brightness and stability. A major drawback with the use of photostabilizing buffers, however, is that they cannot be used in live cell imaging. In this paper, we tested the performance of self-healing organic fluorophores, which undergo intramolecular photostabilization, in super-resolution microscopy examining both targeted (stimulated emission depletion (STED) microscopy) and stochastic readout (stochastic optical reconstruction microscopy (STORM)). The overall goal of the study was to identify dyes and conditions that lead to improved spatial and temporal resolution of both techniques without the need for mixtures of photostabilizing agents in the imaging buffer. As a result of previously shown superior performance, we identified an ATTO647N-photostabilizer conjugate as a potential candidate for STED microscopy. We have here characterized the photostability and resulting performance of this nitrophenylalanine (NPA) conjugate of ATTO647N on oligonucleotides in STED microscopy. We found that the superior photophysical performance resulted in optimal STED imaging and demonstrated that single-molecule fluorescent transients of individual fluorophores can be obtained with both the excitation- and STED-laser. In similar experiments, we also tested a nitrophenylacetic acid conjugate of STAR635P, another frequently used dye in STED microscopy, and present a characterization of its photophysical properties. Finally, we performed an analysis of the photoswitching kinetics of self-healing Cy5 dyes (containing trolox, cyclooctatetraene and NPA-based stabilizers) in the presence of Tris(2-carboxyethyl) phosphine and cysteamine, which are typically used in STORM microscopy. In line with previous work, we found that intramolecular photostabilization strongly influences photoswitching kinetics and requires careful attention when designing STORM-experiments. In summary, this contribution explores the possibilities and limitations of self-healing dyes in super-resolution microscopy of differing modalities.
关键词： STORM,super-resolution microscopy,fluorescent dyes,STED,fluorescence microscopy
更新于2025-09-09 09:28:46
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Whole-cell, 3D and multi-color STED imaging with exchangeable fluorophores
摘要： We demonstrate STED microscopy of whole bacterial and eukaryotic cells using fluorogenic labels that reversibly bind to their target structure. A constant exchange of labels guarantees the removal of photobleached fluorophores and their replacement by intact fluorophores, thereby circumventing bleaching-related limitations of STED super-resolution imaging. We achieve a constant labeling density and demonstrate a fluorescence signal for long and theoretically unlimited acquisition times. Using this concept, we demonstrate whole-cell, 3D, multi-color and live cell STED microscopy.
关键词： PAINT,fluorogenic labels,multicolor imaging,live-cell STED microscopy,volumetric imaging,exchange-based STED microscopy
更新于2025-09-04 15:30:14
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Triarylmethane Fluorophores Resistant to Oxidative Photobluing
摘要： Spectral stability of small-molecule fluorescent probes is required for correct interpretation and reproducibility of multicolor fluorescence imaging data, in particular under high (de)excitation light intensities of super-resolution imaging or in single-molecule applications. We propose a synthetic approach to a series of spectrally stable rhodamine fluorophores based on sequential Ru- and Cu-catalyzed transformations, evaluate their stability against photobleaching and photoconversion in context of other fluorophores using chemometric analysis, and demonstrate chemical reactivity of fluorophore photoproducts. The substitution patterns providing the photoconversion-resistant triarylmethane fluorophores have been identified, and the applicability of non-bluing labels in live-cell STED nanoscopy is demonstrated.
关键词： STED nanoscopy,photostability,triarylmethane fluorophores,rhodamine fluorophores,oxidative photobluing
更新于2025-09-04 15:30:14
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Super-resolution microscopy and empirically validated autocorrelation image analysis discriminates microstructures of dairy derived gels
摘要： The food industry must capitalise on advancing technologies in order to optimise the potential from emerging ingredient technologies. These can aid in product optimisation and provide quantitative empirical data to which there is a fundamental physical understanding. Super-resolution microscopy provides a tool to characterise the microstructure of complex colloidal materials under near native conditions. Coherent Anti-Stokes Raman Scattering (CARS) microscopy was used to show the presence of fluorescent dye required for imaging does not affect gel microstructure and super-resolution Stimulated Emission Depletion (STED) microscopy is used to image four dairy derived gels. Image analysis has been developed based on 2D spatial autocorrelation, and a model that extracts parameters corresponding to a typical length of the protein domains and the inter pore distance. The model has been empirically validated through the use of generated images to show the fitting parameters relate to precise physical features. The fractal dimension is extracted from Fourier space analysis. The combination of STED microscopy and image analysis is sensitive enough to significantly differentiate samples based on whether gels were made from fresh or reconstituted milk, and whether gelation was induced through acidification or rennet addition. Rheometry shows that the samples exhibit different macroscopic behaviours, and these differences become increasingly significant with time. Samples can be differentiated earlier in the gelation process with imaging as compared to rheometry. This highlights the potential of STED imaging and image analysis to characterise the size of protein domains, pore spacing and the fractal dimensions of microstructures to aid product optimisation.
关键词： Stimulated Emission Depletion (STED) microscopy,Super-resolution microscopy,Fractal dimension,Coherent Anti-stokes Raman Scattering (CARS) microscopy,2D spatial autocorrelation analysis
更新于2025-09-04 15:30:14