21,496 research outputs found

    Electroencephalographic field influence on calcium momentum waves

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    Macroscopic EEG fields can be an explicit top-down neocortical mechanism that directly drives bottom-up processes that describe memory, attention, and other neuronal processes. The top-down mechanism considered are macrocolumnar EEG firings in neocortex, as described by a statistical mechanics of neocortical interactions (SMNI), developed as a magnetic vector potential A\mathbf{A}. The bottom-up process considered are Ca2+\mathrm{Ca}^{2+} waves prominent in synaptic and extracellular processes that are considered to greatly influence neuronal firings. Here, the complimentary effects are considered, i.e., the influence of A\mathbf{A} on Ca2+\mathrm{Ca}^{2+} momentum, p\mathbf{p}. The canonical momentum of a charged particle in an electromagnetic field, Π=p+qA\mathbf{\Pi} = \mathbf{p} + q \mathbf{A} (SI units), is calculated, where the charge of Ca2+\mathrm{Ca}^{2+} is q=−2eq = - 2 e, ee is the magnitude of the charge of an electron. Calculations demonstrate that macroscopic EEG A\mathbf{A} can be quite influential on the momentum p\mathbf{p} of Ca2+\mathrm{Ca}^{2+} ions, in both classical and quantum mechanics. Molecular scales of Ca2+\mathrm{Ca}^{2+} wave dynamics are coupled with A\mathbf{A} fields developed at macroscopic regional scales measured by coherent neuronal firing activity measured by scalp EEG. The project has three main aspects: fitting A\mathbf{A} models to EEG data as reported here, building tripartite models to develop A\mathbf{A} models, and studying long coherence times of Ca2+\mathrm{Ca}^{2+} waves in the presence of A\mathbf{A} due to coherent neuronal firings measured by scalp EEG. The SMNI model supports a mechanism wherein the p+qA\mathbf{p} + q \mathbf{A} interaction at tripartite synapses, via a dynamic centering mechanism (DCM) to control background synaptic activity, acts to maintain short-term memory (STM) during states of selective attention.Comment: Final draft. http://ingber.com/smni14_eeg_ca.pdf may be updated more frequentl

    ProtNN: Fast and Accurate Nearest Neighbor Protein Function Prediction based on Graph Embedding in Structural and Topological Space

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    Studying the function of proteins is important for understanding the molecular mechanisms of life. The number of publicly available protein structures has increasingly become extremely large. Still, the determination of the function of a protein structure remains a difficult, costly, and time consuming task. The difficulties are often due to the essential role of spatial and topological structures in the determination of protein functions in living cells. In this paper, we propose ProtNN, a novel approach for protein function prediction. Given an unannotated protein structure and a set of annotated proteins, ProtNN finds the nearest neighbor annotated structures based on protein-graph pairwise similarities. Given a query protein, ProtNN finds the nearest neighbor reference proteins based on a graph representation model and a pairwise similarity between vector embedding of both query and reference protein-graphs in structural and topological spaces. ProtNN assigns to the query protein the function with the highest number of votes across the set of k nearest neighbor reference proteins, where k is a user-defined parameter. Experimental evaluation demonstrates that ProtNN is able to accurately classify several datasets in an extremely fast runtime compared to state-of-the-art approaches. We further show that ProtNN is able to scale up to a whole PDB dataset in a single-process mode with no parallelization, with a gain of thousands order of magnitude of runtime compared to state-of-the-art approaches
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