Single-channel user-capacity calculations for self-organizing cellular systems

1994 ◽  
Vol 42 (12) ◽  
pp. 3137-3143 ◽  
Author(s):  
L.J. Cimini ◽  
G.J. Foschini ◽  
L.A. Shepp
Keyword(s):  
Single Channel ◽  
Cellular Systems ◽  
User Capacity ◽  
Self Organizing

Bio-inspired self-organizing cellular systems

Biosystems ◽  
2008 ◽  
Vol 94 (1-2) ◽  
pp. 164-169 ◽  
Author(s):  
André Stauffer ◽  
Daniel Mange ◽  
Joël Rossier ◽  
Fabien Vannel
Keyword(s):  
Cellular Systems ◽  
Self Organizing

scholarly journals A Game Theoretic Interference Management Scheme in Full Duplex Cellular Systems under Infeasible QoS Requirements

2019 ◽  
Vol 11 (7) ◽  
pp. 156 ◽  
Author(s):  
Ali Y. Al-Zahrani
Keyword(s):  
Interference Cancellation ◽  
Single Channel ◽  
Minimum Energy ◽  
Interference Management ◽  
Research Work ◽  
Cellular Systems ◽  
Full Duplex ◽  
Intercell Interference ◽  
Minimum Energy Consumption ◽  
Game Theoretic

Several emerging mobile applications and services (e.g., autonomous cars) require higher wireless throughput than ever before. This demand stresses the need for investigating novel methods that have the potential to dramatically increase the spectral efficiency (SE) of wireless systems. An evolving approach is the Single-channel full duplex (SCFD) communication where each node may simultaneously receive and transmit over the same frequency channel, and, hence, this could potentially double the current SE figures. In an earlier research work, we derived a model of the signal to interference plus noise ratio (SINR) in an SCFD-based cellular system with imperfect self interference cancellation, and investigated interference management under feasible QoS requirements. In this paper, game theoretic results are exploited to investigate the intercell interference management in SCFD-based cellular networks under infeasible QoS requirements. The investigation starts with a game formulation that captures two different cases. Then, the existence and uniqueness of the Nash equilibrium point are established. After that, a computationally efficient distributed algorithm, which realizes best effort and fair wireless services, is designed. The merit of this scheme is that, when the QoS requirements are feasible, they will be achieved with minimum energy consumption. Results of extensive simulation experiments are presented to show the effectiveness of the proposed schemes.

Self-Organizing Data and Signal Cellular Systems

2011 ◽  
pp. 139-166
Author(s):  
André Stauffer ◽  
Gianluca Tempesti
Keyword(s):  
Cellular Systems ◽  
Self Organizing

scholarly journals Selective Chemical Activation of Piezo1 in Leukemia Cell Membrane: Single Channel Analysis

2021 ◽  
Vol 22 (15) ◽  
pp. 7839
Author(s):  
Valeria Vasileva ◽  
Elena Morachevskaya ◽  
Anastasia Sudarikova ◽  
Yuri Negulyaev ◽  
Vladislav Chubinskiy-Nadezhdin
Keyword(s):  
Cell Membrane ◽  
Patch Clamp ◽  
Lipid Bilayers ◽  
Single Channel ◽  
Chemical Activation ◽  
Leukemia Cell ◽  
K562 Cells ◽  
Cellular Systems ◽  
Suitable Model ◽  
Patch Clamp Technique

Piezo1/2 are mechanosensitive calcium-permeable channels that can be activated by various modes of membrane deformation. The identification of the small molecule Yoda1, a synthetic Piezo1 agonist, revealed the possibility of chemical activation of the channel. Stimulating effects of Yoda1 on Piezo1 have been mainly documented using over-expressing cellular systems or channel proteins incorporated in artificial lipid bilayers. However, the activating effect of Yoda1 on native Piezo1 channels in the plasma membrane of living cells remains generally undefined, despite the increasing number of studies in which the agonist is utilized as a functional tool to reveal the contribution of Piezo1 to cellular reactions. In the current study, we used the human myeloid leukemia K562 cell line as a suitable model to examine chemically induced Piezo1 activity with the use of the patch-clamp technique in various specific modes. The functional expression of Piezo1 in leukemia cells was evidenced using a combinative approach, including single channel patch-clamp measurements. Utilizing our established single-current whole-cell assay on K562 cells, we have shown, for the first time, the selective real-time chemical activation of endogenously expressed Piezo1. Extracellular application of 0.5–1 µM Yoda1 effectively stimulated single Piezo1 currents in the cell membrane.

Data Acquisition and Handling Unit for a Quantitative Use of Electron Energy Loss Spectroscopy

1977 ◽  
Vol 35 ◽  
pp. 232-233 ◽  
Author(s):  
P. Trebbia ◽  
P. Ballongue ◽  
C. Colliex
Keyword(s):  
Electron Microscope ◽  
Energy Loss ◽  
Electron Energy ◽  
Electron Energy Loss Spectroscopy ◽  
Single Channel ◽  
Detection System ◽  
Surface Barrier ◽  
Solid State Detector ◽  
Electrostatic Mirror ◽  
Electron Energy Loss

An effective use of electron energy loss spectroscopy for chemical characterization of selected areas in the electron microscope can only be achieved with the development of quantitative measurements capabilities.The experimental assembly, which is sketched in Fig.l, has therefore been carried out. It comprises four main elements.The analytical transmission electron microscope is a conventional microscope fitted with a Castaing and Henry dispersive unit (magnetic prism and electrostatic mirror). Recent modifications include the improvement of the vacuum in the specimen chamber (below 10-6 torr) and the adaptation of a new electrostatic mirror.The detection system, similar to the one described by Hermann et al (1), is located in a separate chamber below the fluorescent screen which visualizes the energy loss spectrum. Variable apertures select the electrons, which have lost an energy AE within an energy window smaller than 1 eV, in front of a surface barrier solid state detector RTC BPY 52 100 S.Q. The saw tooth signal delivered by a charge sensitive preamplifier (decay time of 5.10-5 S) is amplified, shaped into a gaussian profile through an active filter and counted by a single channel analyser.

Label-free, mass-sensitive single-molecule imaging using interferometric scattering microscopy

2020 ◽  
Author(s):  
Nikolas Hundt
Keyword(s):  
Single Molecule ◽  
Cellular Systems ◽  
Single Molecule Imaging ◽  
Label Free ◽  
Measurement Sensitivity ◽  
Mass Distributions ◽  
Quantitative Measurements ◽  
Contrast Mechanism ◽  
Cellular Components ◽  
Scattering Signal

Abstract Single-molecule imaging has mostly been restricted to the use of fluorescence labelling as a contrast mechanism due to its superior ability to visualise molecules of interest on top of an overwhelming background of other molecules. Recently, interferometric scattering (iSCAT) microscopy has demonstrated the detection and imaging of single biomolecules based on light scattering without the need for fluorescent labels. Significant improvements in measurement sensitivity combined with a dependence of scattering signal on object size have led to the development of mass photometry, a technique that measures the mass of individual molecules and thereby determines mass distributions of biomolecule samples in solution. The experimental simplicity of mass photometry makes it a powerful tool to analyse biomolecular equilibria quantitatively with low sample consumption within minutes. When used for label-free imaging of reconstituted or cellular systems, the strict size-dependence of the iSCAT signal enables quantitative measurements of processes at size scales reaching from single-molecule observations during complex assembly up to mesoscopic dynamics of cellular components and extracellular protrusions. In this review, I would like to introduce the principles of this emerging imaging technology and discuss examples that show how mass-sensitive iSCAT can be used as a strong complement to other routine techniques in biochemistry.

Sign in / Sign up

Export Citation Format

Share Document