3D structured illumination microscope using a spinning disk [Invited].

Three-dimensional (3D) structured illumination microscopy (SIM) improves spatial resolution by a factor of two in both lateral and axial directions. However, the adoption of 3D SIM is limited by low imaging speed, susceptibility to out-of-focus light, and likelihood of reconstruction errors. Here we present a novel approach for 3D SIM using a spinning disk. The disk generates a 3D lattice illumination pattern on the sample and optically reconstructs super-resolved images in real time. This technique achieves a 2-times resolution improvement with a speed up to 100 frames per second while physically rejecting 90% of the background signal.

Structured illumination microscopy with a phase-modulated spinning disk for optical sectioning.

Among various super-resolution microscopic techniques, structured illumination microscopy (SIM) stands out for live-cell imaging because of its higher imaging speed. However, conventional SIM lacks optical sectioning capability. Here we demonstrate a new, to the best of our knowledge, approach using a phase-modulated spinning disk (PMSD) that enhances the optical sectioning capability of SIM. The PMSD consists of a pinhole array for confocal imaging and a transparent polymer layer for light phase modulation. The light phase modulation was designed to cancel the zeroth-order diffracted beam and create a sharp lattice illumination pattern using the interference of four first-order diffracted beams. In the detection optical path, the PMSD serves as a spatial filter to physically reject about 80% of the out-of-focus signals, an approach that allows for real-time optical reconstruction of super-resolved images with enhanced contrast. Furthermore, the simplicity of the design makes it easy to upgrade a conventional fluorescence microscope to a PMSD SIM system.

The nanoscale organization of Nipah virus matrix protein revealed by super-resolution microscopy.

The matrix proteins (M) of many enveloped RNA viruses mediate virus assembly and budding. However, it remains poorly understood how M are involved in virus budding and how they interact with envelope proteins. Here, we show that the expression level of Nipah (NiV) M in particles produced by the host cells deviates from a gamma distribution and does not reflect that of the host cells, indicating assembly of the NiV-M in the process. Our data reveal that NiV-M affects the circularity of the particles while the NiV envelope proteins do not. The organization of NiV envelope proteins on the membrane of the particles is similar to those that do not express NiV-M, suggesting that NiV-M does not directly interact with the envelope proteins during assembly and budding.

The DFT Quest for Possible Reaction Pathways, Catalytic Species, and Regioselectivity in the InCl3-Catalyzed Cycloaddition of N-Tosyl Formaldimine with Olefins or Allenes.

The present work focuses on a theoretical investigation of the plausible mechanism, determination of catalytically active species, and understanding of the regioselectivity in the InCl3-catalyzed cycloaddition of N-tosyl formaldimine with alkenes or allenes. InCl3 and InCl2+ coordinated by dichloroethane (InCl2+-DCE) were investigated as model catalytic systems. DFT data supported that InCl2+-DCE represent the plausible in situ generated catalytic species. The catalytic cycle starts from the coordination of N-tosyl formaldimine to InCl2+-DCE, generating an In-complexed iminium intermediate. This then undergoes intermolecular reaction (aza-Prins) with alkene substrate to form a carbocation intermediate, which is chemoselectively attacked by the second N-tosyl formaldimine molecule to form a formaldiminium intermediate. In a final step, this intermediate undergoes the ring closure, leading to hexahydropyrimidine along with the regeneration of catalyst. In addition, our DFT results indicate that N-tosyl formaldimine not only acts as a reactant but also accelerates the 1,3-H-shift as a proton acceptor, giving an experimentally observed allylamide product. Also, the "iminium/alkene/imine" path was supported by calculation results for diastereoselective [2 + 2 + 2] reaction using an internal alkene. Finally, the regioselectivity of the InCl3-catalyzed cycloaddition using allenes along with N-tosyl formaldimine was also analyzed.

Identification of associated SSR markers for yield component and fiber quality traits based on frame map and Upland cotton collections.

Detecting QTLs (quantitative trait loci) that enhance cotton yield and fiber quality traits and accelerate breeding has been the focus of many cotton breeders. In the present study, 359 SSR (simple sequence repeat) markers were used for the association mapping of 241 Upland cotton collections. A total of 333 markers, representing 733 polymorphic loci, were detected. The average linkage disequilibrium (LD) decay distances were 8.58 cM (r2 > 0.1) and 5.76 cM (r2 > 0.2). 241 collections were arranged into two subgroups using STRUCTURE software. Mixed linear modeling (MLM) methods (with population structure (Q) and relative kinship matrix (K)) were applied to analyze four phenotypic datasets obtained from four environments (two different locations and two years). Forty-six markers associated with the number of bolls per plant (NB), boll weight (BW), lint percentage (LP), fiber length (FL), fiber strength (FS) and fiber micornaire value (FM) were repeatedly detected in at least two environments. Of 46 associated markers, 32 were identified as new association markers, and 14 had been previously reported in the literature. Nine association markers were near QTLs (at a distance of less than 1-2 LD decay on the reference map) that had been previously described. These results provide new useful markers for marker-assisted selection in breeding programs and new insights for understanding the genetic basis of Upland cotton yields and fiber quality traits at the whole-genome level.

[Epidemiologic research on the clinical features of patients with cervical spondylosis].

OBJECTIVE: To investigate the clinical features of patients with cervical spondylosis. METHODS: Questionnaires were provided and X rays were examined in 1 009 people with different occupations, ages, and sexes. RESULTS: All the patients were diagnozed as cervical spondylosis. Of them, cadres occupied 78.83%, technologists made up 74.21%, and accountants 58.70%; nervous and long-time working people accounted for 59.75%; high and middle pillow-lovers occupied 80.03%. Imaging features: most of the degenerative changes of cervical spine were located between C5-6 (40.79%), C4-5 (26.29%), and C6-7 (18.20%). Patients with vertebral osteophyte were 65.75%, intervertebral space narrow 36.87%, intervertebral foramen narrow 29.19%, and physiological curve change 31.03%. CONCLUSION: This epidemiologic investigation is important, which can further understand the cause of cervical spondyiosis, and strengthen its prevention and treatment.