Non-linear Rheology of Lyotropic Lamellar Phases

この論文は国立情報学研究所の電子図書館事業により電子化されました。研究会報告スメクティック液晶やリオトロピック系のラメラ相のような一次元周期構造を有する系のレオロジーを議論する。我々は転位ループの運動が散逸に寄与すると仮定し、そのダイナミクスを考察することにより、ずり速度と応力の関係を与えるスケーリング則を導いた。さらに非イオン界面活性剤(C_E_5)水溶液におけるラメラ相のレオロジー測定を行い、理論的な予測の検証を行った。その結果、予測に近いスケーリング則を確認するとともに、ずり速度の揺らぎが平均のずり速度に比例するという興味深い現象を発見した

Spatiotemporal Scan and Age-Period-Cohort Analysis of Hepatitis C Virus in Henan, China: 2005–2012

Background: Studies have shown that hepatitis C virus (HCV) infection increased during the past decades in China. However, little evidence is available on when, where, and who were infected with HCV. There are gaps in knowledge on the epidemiological burden and evolution of the HCV epidemic in China. Methods: Data on HCV cases were collected by the disease surveillance system from 2005 to 2012 to explore the epidemic in Henan province. Spatiotemporal scan statistics and age-period-cohort (APC) model were used to examine the effects of age, period, birth cohort, and spatiotemporal clustering. Results: 177,171 HCV cases were reported in Henan province between 2005 and 2012. APC modelling showed that the HCV reported rates significantly increased in people aged > 50 years. A moderate increase in HCV reported rates was observed for females aged about 25 years. HCV reported rates increased over the study period. Infection rates were greatest among people born between 1960 and 1980. People born around 1970 had the highest relative risk of HCV infection. Women born between 1960 and 1980 had a five-fold increase in HCV infection rates compared to men, for the same birth cohort. Spatiotemporal mapping showed major clustering of cases in northern Henan, which probably evolved much earlier than other areas in the province. Conclusions: Spatiotemporal mapping and APC methods are useful to help delineate the evolution of the HCV epidemic. Birth cohort should be part of the criteria screening programmes for HCV in order to identify those at highest risk of infection and unaware of their status. As Henan is unique in the transmission route for HCV, these methods should be used in other high burden provinces to help identify subpopulations at risk

Computational design of transmembrane pores.

Transmembrane channels and pores have key roles in fundamental biological processes1 and in biotechnological applications such as DNA nanopore sequencing2-4, resulting in considerable interest in the design of pore-containing proteins. Synthetic amphiphilic peptides have been found to form ion channels5,6, and there have been recent advances in de novo membrane protein design7,8 and in redesigning naturally occurring channel-containing proteins9,10. However, the de novo design of stable, well-defined transmembrane protein pores that are capable of conducting ions selectively or are large enough to enable the passage of small-molecule fluorophores remains an outstanding challenge11,12. Here we report the computational design of protein pores formed by two concentric rings of α-helices that are stable and monodisperse in both their water-soluble and their transmembrane forms. Crystal structures of the water-soluble forms of a 12-helical pore and a 16-helical pore closely match the computational design models. Patch-clamp electrophysiology experiments show that, when expressed in insect cells, the transmembrane form of the 12-helix pore enables the passage of ions across the membrane with high selectivity for potassium over sodium; ion passage is blocked by specific chemical modification at the pore entrance. When incorporated into liposomes using in vitro protein synthesis, the transmembrane form of the 16-helix pore-but not the 12-helix pore-enables the passage of biotinylated Alexa Fluor 488. A cryo-electron microscopy structure of the 16-helix transmembrane pore closely matches the design model. The ability to produce structurally and functionally well-defined transmembrane pores opens the door to the creation of designer channels and pores for a wide variety of applications

Crystal structure and biochemical analyses reveal Beclin 1 as a novel membrane binding protein

The Beclin 1 gene is a haplo-insufficient tumor suppressor and plays an essential role in autophagy. However, the molecular mechanism by which Beclin 1 functions remains largely unknown. Here we report the crystal structure of the evolutionarily conserved domain (ECD) of Beclin 1 at 1.6 Å resolution. Beclin 1 ECD exhibits a previously unreported fold, with three structural repeats arranged symmetrically around a central axis. Beclin 1 ECD defines a novel class of membrane-binding domain, with a strong preference for lipid membrane enriched with cardiolipin. The tip of a surface loop in Beclin 1 ECD, comprising three aromatic amino acids, acts as a hydrophobic finger to associate with lipid membrane, consequently resulting in the deformation of membrane and liposomes. Mutation of these aromatic residues rendered Beclin 1 unable to stably associate with lipid membrane in vitro and unable to fully rescue autophagy in Beclin 1-knockdown cells in vivo. These observations form an important framework for deciphering the biological functions of Beclin 1

Solid Nanoporosity Governs Catalytic CO2 and N2 Reduction

Global demand for green and clean energy is increasing day by day owing to ongoing developments by the human race that are changing the face of the earth at a rate faster than ever. Exploring alternative sources of energy to replace fossil fuel consumption has become even more vital to control the growing concentration of CO2, and reduction of CO2 into CO or other useful hydrocarbons (e.g., C1 and C>2 products), as well as reduction of N2 into ammonia, can greatly help in this regard. Various materials have been developed for the reduction of CO2 and N2. The introduction of pores in these materials by porosity engineering has been demonstrated to be highly effective in increasing the efficiency of the involved redox reactions, over 40% increment for CO2 reduction to date, by providing an increased number of exposed facets, kinks, edges, and catalytically active sites of catalysts. By shaping the surface porous structure, the selectivity of the redox reaction can also be enhanced. In order to better understand this area benefiting rational design for future solutions, this review systematically summarizes and constructively discusses the porosity engineering in catalytic materials, including various synthesis methods, characterization of porous materials, and the effects of porosity on performance of CO2 reduction and N2 reduction.F.N., P.L., J.Z., Z.L., and Z.Y. received funding from the Australian Research Council (DP190100295, LE190100014), the ANU Futures Scheme (Q4601024), and ANU Global Research Partnership Scheme (R468504649). Y.D. received funding from National Natural Science Foundation of China (21971117, 21522106), Functional Research Funds for the Central Universities, Nankai University (63186005), Tianjin Key Lab for Rare Earth Materials and Applications (ZB19500202), and 111 Project (No. B18030) from China. F.N. received funding from International Research Support Initiative Program (No. 8405) HEC, Pakistan

Synthesis of polyoxometalates derived bifunctional catalyst towards efficient overall water splitting in neutral and alkaline medium

The development of efficient hydrogen evolution and oxygen evolution reactions bifunctional electrocatalyst for overall water splitting is highly desired but still a great challenge, especially under neutral condition. With the unique properties of polyoxometalate and MOFs materials as well as rich transition metal contents, herein we successfully synthesize a novel bi-phase structure of cobalt and molybdenum carbide coated with nitrogen-doped graphite (Co-Mo2C@NC) which possesses excellent activity as water splitting electrocatalyst at neutral pH. This noble metal-free, bi-phase electrocatalyst exhibits Hydrogen Evolution Reaction (HER) and Oxygen Evolution Reaction (OER) overpotentials of 260 mV and 440 mV at 10 mA cm(-2), respectively. The two-electrode system using Co-Mo2C@NC as both the anode and cathode drives 10 mA cm(-2) at a cell voltage of 1.83 V with a remarkable long-term stability. Besides, the Co-Mo2C@NC also shows promising activity in alkaline condition that reaches 10 mA cm(-2) at a cell voltage of 1.66 V. This work paves a new avenue to the design of the unique, economic and promising non-noble metal electrode materials for practical applications in the electrochemical energy storage and conversion devices. (C) 2018 Elsevier Inc. All rights reserved