215 research outputs found

    Controlling colloidal phase transitions with critical Casimir forces

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    The critical Casimir effect provides a thermodynamic analogue of the well-known quantum mechanical Casimir effect. It acts between two surfaces immersed in a critical binary liquid mixture, and results from the confinement of concentration fluctuations of the solvent. Unlike the quantum mechanical effect, the magnitude and range of this attraction can be adjusted with temperature via the solvent correlation length, thus offering new opportunities for the assembly of nano and micron-scale structures. Here, we demonstrate the active assembly control of equilibrium phases using critical Casimir forces. We guide colloidal particles into analogues of molecular liquid and solid phases via exquisite control over their interactions. By measuring the critical Casimir particle pair potential directly from density fluctuations in the colloidal gas, we obtain insight into liquefaction at small scales: We apply the Van der Waals model of molecular liquefaction and show that the colloidal gas-liquid condensation is accurately described by the Van der Waals theory, even on the scale of a few particles. These results open up new possibilities in the active assembly control of micro and nanostructures

    Strain-Rate Frequency Superposition (SRFS) - A rheological probe of structural relaxation in soft materials

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    The rheological properties of soft materials often exhibit surprisingly universal linear and non-linear features. Here we show that these properties can be unified by considering the effect of the strain-rate amplitude on the structural relaxation of the material. We present a new form of oscillatory rheology, Strain-Rate Frequency Superposition (SRFS), where the strain-rate amplitude is fixed as the frequency is varied. We show that SRFS can isolate the response due to structural relaxation, even when it occurs at frequencies too low to be accessible with standard techniques.Comment: 4 pages, 4 figure

    Daisy: Data analysis integrated software system for X-ray experiments

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    Daisy (Data Analysis Integrated Software System) has been designed for the analysis and visualization of the X-ray experiments. To address an extensive range of Chinese radiation facilities community's requirements from purely algorithmic problems to scientific computing infrastructure, Daisy sets up a cloud-native platform to support on-site data analysis services with fast feedback and interaction. The plugs-in based application is convenient to process the expected high throughput data flow in parallel at next-generation facilities such as the High Energy Photon Source (HEPS). The objectives, functionality and architecture of Daisy are described in this article

    Intraocular Pressure Changes: An Important Determinant of the Biocompatibility of Intravitreous Implants

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    Background: In recent years, research efforts exploring the possibility of using biomaterial nanoparticles for intravitreous drug delivery has increased significantly. However, little is known about the effect of material properties on intravitreous tissue responses. Principal Findings: To find the answer, nanoparticles made of hyaluronic acid (HA), poly (l-lactic acid) (PLLA), polystyrene (PS), and Poly N-isopropyl acrylamide (PNIPAM) were tested using intravitreous rabbit implantation model. Shortly after implantation, we found that most of the implants accumulated in the trabecular meshwork area followed by clearance from the vitreous. Interestingly, substantial reduction of intraocular pressure (IOP) was observed in eyes implanted with particles made of PS, PNIPAM and PLLA, but not HA nanoparticles and buffered salt solution control. On the other hand, based on histology, we found that the particle implantation had no influence on cornea, iris and even retina. Surprisingly, substantial CD11b+ inflammatory cells were found to accumulate in the trabecular meshwork area in some animals. In addition, there was a good relationship between recruited CD11b+ cells and IOP reduction. Conclusions: Overall, the results reveal the potential influence of nanoparticle material properties on IOP reduction and inflammatory responses in trabecular meshwork. Such interactions may be critical for the development of future ocula

    Study on the dynamic characteristics of planetary gear transmission mechanism of metal cold rolling mill

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    Using the parametric modelling feature in Solidworks software, a three-dimensional solid model of a planetary gearbox with linear reciprocating motion of the output shaft was constructed. By conducting theoretical calculations related to the kinematics of the transmission system and combining Adams virtual prototyping simulation technology, a dynamic simulation model of the planetary gear transmission mechanism was established to analyse the motion laws and dynamic characteristics. The simulation results were compared and analysed against the theoretical calculation results, and they showed good agreement and consistency. The study also investigated the impact of counterweights on the inertia forces and moments of the output shaft in the transmission mechanism. The results indicated that adding counterweights effectively reduced the inertia impact caused by inertia forces at the start and end positions of the stroke, as well as the inertia torque caused by changes in angular acceleration during the startup and stopping phases, thereby enhancing the smooth operation of the mechanism. Additionally, different thicknesses of counterweights had varying effects on balancing the inertia forces and moments of the output shaft. The study aimed to find the optimal thickness of counterweights to achieve the best balance effect. Furthermore, the study examined the influence of different speeds of the driving gear on the inertia forces of the output shaft. The results showed that at a driving gear speed of 1500 rpm, the horizontal thrust generated by the output shaft was 63566 N, which could provide the required thrust for the rolling mill operation, and the inertia forces of the output shaft tended to stabilize

    Spag16, an Axonemal Central Apparatus Gene, Encodes a Male Germ Cell Nuclear Speckle Protein that Regulates SPAG16 mRNA Expression

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    Spag16 is the murine orthologue of Chlamydomonas reinhardtii PF20, a protein known to be essential to the structure and function of the “9+2” axoneme. In Chlamydomonas, the PF20 gene encodes a single protein present in the central pair of the axoneme. Loss of PF20 prevents central pair assembly/integrity and results in flagellar paralysis. Here we demonstrate that the murine Spag16 gene encodes two proteins: 71 kDa SPAG16L, which is found in all murine cells with motile cilia or flagella, and 35 kDa SPAG16S, representing the C terminus of SPAG16L, which is expressed only in male germ cells, and is predominantly found in specific regions within the nucleus that also contain SC35, a known marker of nuclear speckles enriched in pre-mRNA splicing factors. SPAG16S expression precedes expression of SPAG16L. Mice homozygous for a knockout of SPAG16L alone are infertile, but show no abnormalities in spermatogenesis. Mice chimeric for a mutation deleting the transcripts for both SPAG16L and SPAG16S have a profound defect in spermatogenesis. We show here that transduction of SPAG16S into cultured dispersed mouse male germ cells and BEAS-2B human bronchial epithelial cells increases SPAG16L expression, but has no effect on the expression of several other axoneme components. We also demonstrate that the Spag16L promoter shows increased activity in the presence of SPAG16S. The distinct nuclear localization of SPAG16S and its ability to modulate Spag16L mRNA expression suggest that SPAG16S plays an important role in the gene expression machinery of male germ cells. This is a unique example of a highly conserved axonemal protein gene that encodes two protein products with different functions

    Mouse RC/BTB2, a Member of the RCC1 Superfamily, Localizes to Spermatid Acrosomal Vesicles

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    Mouse RC/BTB2 is an unstudied protein of the RCC1 (Regulator of Chromosome Condensation) superfamily. Because of the significant remodeling of chromatin that occurs during spermiogenesis, we characterized the expression and localization of mouse RC/BTB2 in the testis and male germ cells. The Rc/btb2 gene yields two major transcripts: 2.3 kb Rc/btb2-s, present in most somatic tissues examined; and 2.5 kb Rc/btb2-t, which contains a unique non-translated exon in its 5′-UTR that is only detected in the testis. During the first wave of spermatogenesis, Rc/btb2-t mRNA is expressed from day 8 after birth, reaching highest levels of expression at day 30 after birth. The full-length protein contains three RCC1 domains in the N-terminus, and a BTB domain in the C-terminus. In the testis, the protein is detectable from day 12, but is progressively up-regulated to day 30 and day 42 after birth. In spermatids, some of the protein co-localizes with acrosomal markers sp56 and peanut lectin, indicating that it is an acrosomal protein. A GFP-tagged RCC1 domain is present throughout the cytoplasm of transfected CHO cells. However, both GFP-tagged, full-length RC/BTB2 and a GFP-tagged BTB domain localize to vesicles in close proximity to the nuclear membrane, suggesting that the BTB domain might play a role in mediating full-length RC/BTB2 localization. Since RCC1 domains associate with Ran, a small GTPase that regulates molecular trafficking, it is possible that RC/BTB2 plays a role in transporting proteins during acrosome formation
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