28 research outputs found
Hydrogen-assisted fracture of additively manufactured type 304L austenitic stainless steel
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From Isotropic to Anisotropic Side Chain Representations: Comparison of Three Models for Residue Contact Estimation
The criterion to determine residue contact is a fundamental problem in deriving knowledge-based mean-force potential energy calculations for protein structures. A frequently used criterion is to require the side chain center-to-center distance or the -to- atom distance to be within a pre-determined cutoff distance. However, the spatially anisotropic nature of the side chain determines that it is challenging to identify the contact pairs. This study compares three side chain contact models: the Atom Distance criteria (ADC) model, the Isotropic Sphere Side chain (ISS) model and the Anisotropic Ellipsoid Side chain (AES) model using 424 high resolution protein structures in the Protein Data Bank. The results indicate that the ADC model is the most accurate and ISS is the worst. The AES model eliminates about 95% of the incorrectly counted contact-pairs in the ISS model. Algorithm analysis shows that AES model is the most computational intensive while ADC model has moderate computational cost. We derived a dataset of the mis-estimated contact pairs by AES model. The most misjudged pairs are Arg-Glu, Arg-Asp and Arg-Tyr. Such a dataset can be useful for developing the improved AES model by incorporating the pair-specific information for the cutoff distance
EVOLUTION OF NANOSCALE Al<SUB>3</SUB>(Zr<SUB><I>x</I></SUB>Er<SUB>1-<I>x</I></SUB>) PRECIPI-TATES IN Al--6Mg--0.7Mn--0.1Zr--0.3Er ALLOY ALLOY DURING ANNEALING
Solid solution decomposition mechanisms in cast and microcrystalline Al-Sc alloys: I. Experimental studies
Mobility-Selected Ion Trapping and Enrichment Using Structures for Lossless Ion Manipulations
Regulation of endothelial intracellular adenosine via adenosine kinase epigenetically modulates vascular inflammation
The molecular mechanisms underlying vascular inflammation and associated inflammatory vascular diseases are not well defined. Here we show that endothelial intracellular adenosine and its key regulator adenosine kinase (ADK) play important roles in vascular inflammation. Pro-inflammatory stimuli lead to endothelial inflammation by increasing endothelial ADK expression, reducing the level of intracellular adenosine in endothelial cells, and activating the transmethylation pathway through increasing the association of ADK with S-adenosylhomocysteine (SAH) hydrolase (SAHH). Increasing intracellular adenosine by genetic ADK knockdown or exogenous adenosine reduces activation of the transmethylation pathway and attenuates the endothelial inflammatory response. In addition, loss of endothelial ADK in mice leads to reduced atherosclerosis and affords protection against ischemia/reperfusion injury of the cerebral cortex. Taken together, these results demonstrate that intracellular adenosine, which is controlled by the key molecular regulator ADK, influences endothelial inflammation and vascular inflammatory diseases.National Key Basic Research Program of China [2012CB910402]; National Natural Science Foundation of China [81400826]; Guangdong Natural Science Foundation [2014A030312004]; Shenzhen Science and Technology Innovation Committee [20160517084712652, 20160503001803075, JCYJ20140903101709818, JSGG20140717102922014]; Shenzhen Peacock Program [KQCX2015032709315529]; American Heart Association [15POST22810024, 16GRNT30510010]; National Institutes of Health [HL095556, R01DK095862]SCI(E)ARTICLE