Lecithin nanoparticles enhance the cryosurvival of caprine sperm

P. 38-44This study was designed to compare the effects on goat spermatozoa cryosurvival of nano-lecithin-based (NL), lecithin-based (L) and egg yolk-based (EY) extenders. Ejaculates were collected from four fertile goats using artificial vagina and diluted with nine extenders. NL and L were tested at concentrations 1%, 2%, 3% and 4% (w/v), versus 15% (v/v) egg yolk-based extender. Overall, sperm quality (higher motility, viability and HOST, and lower apoptosis) was higher for NL than for L treatments (P < 0.05 for most cases, except for 1%). NL at 1% and especially at 4% showed lower motility and viability than 2% or 3% NL. NL at 2% achieved a better performance (P < 0.05) than EY for VCL (131.5 ± 1.3 vs. 120.3 ± 1.9 μm/s), VSL (43.9 ± 1.5 vs. 35.8 ± 1.4 μm/s), LIN (35.7 ± 0.6 vs. 29.3 ± 0.8%), WOB (47.0 ± 0.5 vs. 43.9 ± 0.9%) and viability (66.4 ± 1.7 vs. 52.7 ± 1.9%). Late apoptotic spermatozoa were also lower in 2% NL compared to EY (16.0 ± 0.5 vs. 26.3 ± 1.1%, P < 0.001). EY and 2% NL were compared in an IVF trial, with no significant differences in cleavage (68.8 vs. 70.8%) or blastocyst ratios (21.3 vs. 20.8%). In conclusion, using 2% nanolecithin in semen dilution could improve sperm cryosurvival of goat.S

Theoretical study of fMet-tRNA and fAla-tRNA structures by using quantum calculation

AbstractIn the prokaryotes, protein synthesis always starts with N-formylmethionine amino acid. Comparison of this amino acid with other amino acids is attempted and that is why formylmethionine is always the first amino acid to begin protein synthesis, in this paper we added a formyl group to alanine amino acid and then studied it when attached to the tRNA molecule and compared this structure with formylmethionine-tRNA structure. The quantum chemical calculations have performed using Gaussian 03 suite of programs. The fAla-tRNA and fMet-tRNA structures have fully optimized at the HF and B3LYP levels with 3–21G∗ and 6–31G∗ basis sets as well as MP2/3–21G∗ level and theoretically solvent effects on the structures were investigated. Then we studied electronic structures of the compounds using Natural Bond Orbital (NBO) analysis and calculated NMR parameters at the gas-phase. Frequency analysis was also calculated at the HF and B3LYP/3-21G∗ levels in the different solvents in 298.15K, 310.15K temperatures and 1.00 atmosphere pressure

A probabilistic approach for pediatric epilepsy diagnosis using brain functional connectivity networks

Background The lives of half a million children in the United States are severely affected due to the alterations in their functional and mental abilities which epilepsy causes. This study aims to introduce a novel decision support system for the diagnosis of pediatric epilepsy based on scalp EEG data in a clinical environment. Methods A new time varying approach for constructing functional connectivity networks (FCNs) of 18 subjects (7 subjects from pediatric control (PC) group and 11 subjects from pediatric epilepsy (PE) group) is implemented by moving a window with overlap to split the EEG signals into a total of 445 multi-channel EEG segments (91 for PC and 354 for PE) and finding the hypothetical functional connectivity strengths among EEG channels. FCNs are then mapped into the form of undirected graphs and subjected to extraction of graph theory based features. An unsupervised labeling technique based on Gaussian mixtures model (GMM) is then used to delineate the pediatric epilepsy group from the control group. Results The study results show the existence of a statistically significant difference (p \u3c 0.0001) between the mean FCNs of PC and PE groups. The system was able to diagnose pediatric epilepsy subjects with the accuracy of 88.8% with 81.8% sensitivity and 100% specificity purely based on exploration of associations among brain cortical regions and without a priori knowledge of diagnosis. Conclusions The current study created the potential of diagnosing epilepsy without need for long EEG recording session and time-consuming visual inspection as conventionally employed

Catalytic cleavage of HEAT and subsequent covalent binding of the tetralone moiety by the SARS-CoV-2 main protease

Here we present the crystal structure of SARS-CoV-2 main protease (Mpro) covalently bound to 2-methyl-1-tetralone. This complex was obtained by co-crystallization of Mpro with HEAT (2-(((4-hydroxyphenethyl)amino)methyl)-3,4-dihydronaphthalen-1(2H)-one) in the framework of a large X-ray crystallographic screening project of Mpro against a drug repurposing library, consisting of 5632 approved drugs or compounds in clinical phase trials. Further investigations showed that HEAT is cleaved by Mpro in an E1cB-like reaction mechanism into 2-methylene-1-tetralone and tyramine. The catalytic Cys145 subsequently binds covalently in a Michael addition to the methylene carbon atom of 2-methylene-1-tetralone. According to this postulated model HEAT is acting in a pro-drug-like fashion. It is metabolized by Mpro, followed by covalent binding of one metabolite to the active site. The structure of the covalent adduct elucidated in this study opens up a new path for developing non-peptidic inhibitors

An empirical investigation of performance overhead in cross-platform mobile development frameworks

The heterogeneity of the leading mobile platforms in terms of user interfaces, user experience, programming language, and ecosystem have made cross-platform development frameworks popular. These aid the creation of mobile applications – apps – that can be executed across the target platforms (typically Android and iOS) with minimal to no platform-specific code. Due to the cost- and time-saving possibilities introduced through adopting such a framework, researchers and practitioners alike have taken an interest in the underlying technologies. Examining the body of knowledge, we, nonetheless, frequently encounter discussions on the drawbacks of these frameworks, especially with regard to the performance of the apps they generate. Motivated by the ongoing discourse and a lack of empirical evidence, we scrutinised the essential piece of the cross-platform frameworks: the bridge enabling cross-platform code to communicate with the underlying operating system and device hardware APIs. The study we present in the article benchmarks and measures the performance of this bridge to reveal its associated overhead in Android apps. The development of the artifacts for this experiment was conducted using five cross-platform development frameworks to generate Android apps, in addition to a baseline native Android app implementation. Our results indicate that – for Android apps – the use of cross-platform frameworks for the development of mobile apps may lead to decreased performance compared to the native development approach. Nevertheless, certain cross-platform frameworks can perform equally well or even better than native on certain metrics which highlights the importance of well-defined technical requirements and specifications for deliberate selection of a cross-platform framework or overall development approach

Geldanamycin anisimycins activate Rho and stimulate Rho- and ROCK-dependent actin stress fiber formation

The journal Molecular Cancer Research is the original source of the material.This article is hosted on a website external to the CBCRA Open Access Archive. Selecting "view/open" will launch the full-text article in another browser window

Effect of Cr on the hydrogen storage and electronic properties of BCC alloys: Experimental and first-principles study

Inventing an effective method to store large amounts of hydrogen at room temperature is one of the key challenges in developing a hydrogen-based economy. Metal hydrides have attracted attention owing to their promising hydrogen storage capabilities. We have systematically studied the structural and electronic properties of mechanically synthesized Ti0.5V1.5-xCrx (0 ≤ x ≤ 0.3) alloys and investigated the influence of the addition of Cr atoms on the hydrogen storage properties of vanadium-rich body-centered-cubic (V-BCC) alloys. X-ray diffraction (XRD) results indicate that all alloys are composed of BCC main phase, with the lattice parameters exhibiting no change following chemical modification. The kinetic measurements have revealed that Cr-containing alloys exhibit improved hydrogen uptake. X-ray photoelectron spectroscopy (XPS) measurements have shown that the addition of Cr has a significant effect on the anti-oxidation properties of V-BCC alloys, increasing their chemical activity and thus enhancing the hydrogen storage properties. Moreover, XPS results elucidate the role of activation of the studied materials. Additionally, the electrochemical properties of the negative electrodes (as part of Ni-MHx secondary batteries) made of Ti0.5V1.4-xNi0.1Crx (0 ≤ x ≤ 0.3) system have been studied by cyclic charge-discharge and demonstrate that doping of the V-BCC alloys with Cr can significantly improve the cycle-life stability of anode that exhibits similar discharge performance up to 50 cycles. First principles simulations are used to analyse the changes in the electronic density of states close to the Fermi level, as a function of Cr concentration, as well as binding energies and structural changes upon hydrogen absorption. Furthermore, ab initio studies confirmed that H absorption is favoured with increasing Cr-content. Our study highlights the importance of the addition of Cr to V-BCC alloys on both solid-gas and electrochemical hydrogenation reactions.Financial assistance from National Science Centre, Poland (no. 2015/17/N/ST8/00271). This project has received funding from the EU-H2020 research and innovation programme under grant agreement No 654360 having benefitted from the access provided by Mateusz Balcerzak in DESY NanoLab (Hamburg, Germany) and ICN2 (Barcelona, Spain) within the framework of the NFFA-Europe Transnational Access Activity. M. Pruneda acknowledges financial support from Spanish MICIU, AEI, and EU FEDER (Grant No. PGC2018-096955-B-C43) and Generalitat de Catalunya (Grant No. 2017SGR1506).Peer reviewe

Effect of Cr on the hydrogen storage and electronic properties of BCC alloys: Experimental and first-principles study

Inventing an effective method to store large amounts of hydrogen at room temperature is one of the key challenges in developing a hydrogen-based economy. Metal hydrides have attracted attention owing to their promising hydrogen storage capabilities. We have systematically studied the structural and electronic properties of mechanically synthesized Ti$_{0.5}$V$_{1.5-x}$Cr$_x$ (0 ≤ x ≤ 0.3) alloys and investigated the influence of the addition of Cr atoms on the hydrogen storage properties of vanadium-rich body-centered-cubic (V-BCC) alloys. X-ray diffraction (XRD) results indicate that all alloys are composed of BCC main phase, with the lattice parameters exhibiting no change following chemical modification. The kinetic measurements have revealed that Cr-containing alloys exhibit improved hydrogen uptake. X-ray photoelectron spectroscopy (XPS) measurements have shown that the addition of Cr has a significant effect on the anti-oxidation properties of V-BCC alloys, increasing their chemical activity and thus enhancing the hydrogen storage properties. Moreover, XPS results elucidate the role of activation of the studied materials. Additionally, the electrochemical properties of the negative electrodes (as part of Ni-MH$_x$ secondary batteries) made of Ti$_{0.5}$V$_{1.4-x}$Ni$_{0.1}$Cr$_x$ (0 ≤ x ≤ 0.3) system have been studied by cyclic charge-discharge and demonstrate that doping of the V-BCC alloys with Cr can significantly improve the cycle-life stability of anode that exhibits similar discharge performance up to 50 cycles. First principles simulations are used to analyse the changes in the electronic density of states close to the Fermi level, as a function of Cr concentration, as well as binding energies and structural changes upon hydrogen absorption. Furthermore, ab initio studies confirmed that H absorption is favoured with increasing Cr-content. Our study highlights the importance of the addition of Cr to V-BCC alloys on both solid-gas and electrochemical hydrogenation reactions