135 research outputs found

    The Engineers' Bookshelf

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    Our perception of an object’s size arises from the integration of multiple sources of visual information including retinal size, perceived distance and its size relative to other objects in the visual field. This constructive process is revealed through a number of classic size illusions such as the Delboeuf Illusion, the Ebbinghaus Illusion and others illustrating size constancy. Here we present a novel variant of the Delbouef and Ebbinghaus size illusions that we have named the Binding Ring Illusion. The illusion is such that the perceived size of a circular array of elements is underestimated when superimposed by a circular contour – a binding ring – and overestimated when the binding ring slightly exceeds the overall size of the array. Here we characterize the stimulus conditions that lead to the illusion, and the perceptual principles that underlie it. Our findings indicate that the perceived size of an array is susceptible to the assimilation of an explicitly defined superimposed contour. Our results also indicate that the assimilation process takes place at a relatively high level in the visual processing stream, after different spatial frequencies have been integrated and global shape has been constructed. We hypothesize that the Binding Ring Illusion arises due to the fact that the size of an array of elements is not explicitly defined and therefore can be influenced (through a process of assimilation) by the presence of a superimposed object that does have an explicit size

    Rigid ball-polyhedra in Euclidean 3-space

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    A ball-polyhedron is the intersection with non-empty interior of finitely many (closed) unit balls in Euclidean 3-space. One can represent the boundary of a ball-polyhedron as the union of vertices, edges, and faces defined in a rather natural way. A ball-polyhedron is called a simple ball-polyhedron if at every vertex exactly three edges meet. Moreover, a ball-polyhedron is called a standard ball-polyhedron if its vertex-edge-face structure is a lattice (with respect to containment). To each edge of a ball-polyhedron one can assign an inner dihedral angle and say that the given ball-polyhedron is locally rigid with respect to its inner dihedral angles if the vertex-edge-face structure of the ball-polyhedron and its inner dihedral angles determine the ball-polyhedron up to congruence locally. The main result of this paper is a Cauchy-type rigidity theorem for ball-polyhedra stating that any simple and standard ball-polyhedron is locally rigid with respect to its inner dihedral angles.Comment: 11 pages, 2 figure

    The Fermat-Torricelli problem in normed planes and spaces

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    We investigate the Fermat-Torricelli problem in d-dimensional real normed spaces or Minkowski spaces, mainly for d=2. Our approach is to study the Fermat-Torricelli locus in a geometric way. We present many new results, as well as give an exposition of known results that are scattered in various sources, with proofs for some of them. Together, these results can be considered to be a minitheory of the Fermat-Torricelli problem in Minkowski spaces and especially in Minkowski planes. This demonstrates that substantial results about locational problems valid for all norms can be found using a geometric approach

    Planar Point Sets Determine Many Pairwise Crossing Segments

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    We show that any set of nn points in general position in the plane determines n1o(1)n^{1-o(1)} pairwise crossing segments. The best previously known lower bound, Ω(n)\Omega\left(\sqrt n\right), was proved more than 25 years ago by Aronov, Erd\H os, Goddard, Kleitman, Klugerman, Pach, and Schulman. Our proof is fully constructive, and extends to dense geometric graphs.Comment: A preliminary version to appear in the proceedings of STOC 201

    On the multiple Borsuk numbers of sets

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    The Borsuk number of a set S of diameter d >0 in Euclidean n-space is the smallest value of m such that S can be partitioned into m sets of diameters less than d. Our aim is to generalize this notion in the following way: The k-fold Borsuk number of such a set S is the smallest value of m such that there is a k-fold cover of S with m sets of diameters less than d. In this paper we characterize the k-fold Borsuk numbers of sets in the Euclidean plane, give bounds for those of centrally symmetric sets, smooth bodies and convex bodies of constant width, and examine them for finite point sets in the Euclidean 3-space.Comment: 16 pages, 3 figure

    Crystal structure of rhodopsin bound to arrestin by femtosecond X-ray laser.

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    G-protein-coupled receptors (GPCRs) signal primarily through G proteins or arrestins. Arrestin binding to GPCRs blocks G protein interaction and redirects signalling to numerous G-protein-independent pathways. Here we report the crystal structure of a constitutively active form of human rhodopsin bound to a pre-activated form of the mouse visual arrestin, determined by serial femtosecond X-ray laser crystallography. Together with extensive biochemical and mutagenesis data, the structure reveals an overall architecture of the rhodopsin-arrestin assembly in which rhodopsin uses distinct structural elements, including transmembrane helix 7 and helix 8, to recruit arrestin. Correspondingly, arrestin adopts the pre-activated conformation, with a ∼20° rotation between the amino and carboxy domains, which opens up a cleft in arrestin to accommodate a short helix formed by the second intracellular loop of rhodopsin. This structure provides a basis for understanding GPCR-mediated arrestin-biased signalling and demonstrates the power of X-ray lasers for advancing the frontiers of structural biology

    Ternary structure reveals mechanism of a membrane diacylglycerol kinase

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    Diacylglycerol kinase catalyses the ATP-dependent conversion of diacylglycerol to phosphatidic acid in the plasma membrane of Escherichia coli. The small size of this integral membrane trimer, which has 121 residues per subunit, means that available protein must be used economically to craft three catalytic and substrate-binding sites centred about the membrane/cytosol interface. How nature has accomplished this extraordinary feat is revealed here in a crystal structure of the kinase captured as a ternary complex with bound lipid substrate and an ATP analogue. Residues, identified as essential for activity by mutagenesis, decorate the active site and are rationalized by the ternary structure. The g-phosphate of the ATP analogue is positioned for direct transfer to the primary hydroxyl of the lipid whose acyl chain is in the membrane. A catalytic mechanism for this unique enzyme is proposed. The active site architecture shows clear evidence of having arisen by convergen
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