29 results match your criteria: "UK [3] Centre for Nanoscience and Quantum Information[Affiliation]"
Nat Commun
May 2014
1] H.H. Wills Physics Laboratory, Tyndall Avenue, Bristol BS8 1TL, UK [2] School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, UK [3] Centre for Nanoscience and Quantum Information, Tyndall Avenue, Bristol BS8 1FD, UK.
Confining a system in a small volume profoundly alters its behaviour. Hitherto, attention has focused on static confinement where the confining wall is fixed such as in porous media. However, adaptive confinement where the wall responds to the interior has clear relevance in biological systems.
View Article and Find Full Text PDFPflugers Arch
February 2013
School of Physiology and Pharmacology, Centre for Nanoscience and Quantum Information and Bristol Heart Institute, University of Bristol, Bristol, UK.
Trimeric intracellular cation-selective (TRIC) channel subtypes, namely TRIC-A and TRIC-B, are derived from distinct genes and distributed throughout the sarco/endoplasmic reticulum (SR/ER) and nuclear membranes. TRIC-A is preferentially expressed at high levels in excitable tissues, while TRIC-B is ubiquitously detected at relatively low levels in various tissues. TRIC channels are composed of ~300 amino acid residues and contain three putative membrane-spanning segments to form a bullet-shaped homo-trimeric assembly.
View Article and Find Full Text PDFNanotechnology
November 2011
Bristol Centre for Nanoscience and Quantum Information, University of Bristol, BS8 1UJ Bristol, UK.
We evaluate the vibrational properties of single-wall carbon nanotube (SWCNT) hetero-junction (HJ) oscillators using a hybrid atomistic-continuum approach validated by molecular mechanics/molecular dynamics simulations. The SWCNT-HJs show a broken symmetry topology of their mode shapes, with striction effects caused on the bending and radial modes by the combined effect of the HJ and the tube with the thinner radius. The single-wall nanotube HJs also show selective mass sensing properties based solely on the geometry and type of the boundary conditions of the specific nanostructure.
View Article and Find Full Text PDFJ Membr Biol
March 2011
School of Physiology and Pharmacology and Centre for Nanoscience and Quantum Information, University of Bristol, Bristol BS81TD, UK.
Phosphorylation of the cardiac ryanodine receptor (RyR2) is thought to be important not only for normal cardiac excitation-contraction coupling but also in exacerbating abnormalities in Ca²+ homeostasis in heart failure. Linking phosphorylation to specific changes in the single-channel function of RyR2 has proved very difficult, yielding much controversy within the field. We therefore investigated the mechanistic changes that take place at the single-channel level after phosphorylating RyR2 and, in particular, the idea that PKA-dependent phosphorylation increases RyR2 sensitivity to cytosolic Ca²+.
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