Channel capacity in cellular systems

Author(s):  
Torleiv Maseng
Sensors ◽  
2021 ◽  
Vol 21 (24) ◽  
pp. 8296
Author(s):  
Cezary Ziółkowski ◽  
Jan M. Kelner ◽  
Jarosław Krygier ◽  
Aniruddha Chandra ◽  
Aleš Prokeš

The basic technology that will determine the expansion of the technical capabilities of fifth generation cellular systems is a massive multiple-input-multiple-output. Therefore, assessing the influence of the antenna beam orientations on the radio channel capacity is very significant. In this case, the effects of mismatching the antenna beam directions are crucial. In this paper, the methodology for evaluating changes in the received signal power level due to beam misalignment for the transmitting and receiving antenna systems is presented. The quantitative assessment of this issue is presented based on simulation studies carried out for an exemplary propagation scenario. For non-line-of-sight (NLOS) conditions, it is shown that the optimal selection of the transmitting and receiving beam directions may ensure an increase in the level of the received signal by several decibels in relation to the coaxial position of the beams. The developed methodology makes it possible to analyze changes in the radio channel capacity versus the signal-to-noise ratio and distance between the transmitter and receiver at optimal and coaxial orientations of antenna beams for various propagation scenarios, considering NLOS conditions. In the paper, the influence of the directional antenna use and their direction choices on the channel capacity versus SNR and the distance between the transmitter and receiver is shown.


2020 ◽  
Author(s):  
Nikolas Hundt

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.


2017 ◽  
Vol E100.B (2) ◽  
pp. 323-335 ◽  
Author(s):  
Kazuhiro HONDA ◽  
Takeshi KITAMURA ◽  
Kun LI ◽  
Koichi OGAWA

2010 ◽  
Vol E93-B (10) ◽  
pp. 2570-2577 ◽  
Author(s):  
Daisuke UCHIDA ◽  
Hiroyuki ARAI ◽  
Yuki INOUE ◽  
Keizo CHO

2012 ◽  
Vol E95-B (4) ◽  
pp. 1190-1197
Author(s):  
Hiromasa FUJII ◽  
Hiroki HARADA ◽  
Shunji MIURA ◽  
Hidetoshi KAYAMA

2013 ◽  
Vol E96.B (5) ◽  
pp. 1141-1148 ◽  
Author(s):  
Dalin ZHANG ◽  
Toshikazu HORI ◽  
Mitoshi FUJIMOTO

2013 ◽  
Vol E96.C (2) ◽  
pp. 171-179 ◽  
Author(s):  
Tatsuhiko IWAKUNI ◽  
Kenji MIYAMOTO ◽  
Takeshi HIGASHINO ◽  
Katsutoshi TSUKAMOTO ◽  
Shozo KOMAKI ◽  
...  

2019 ◽  
Author(s):  
Lukas P Smaga ◽  
Nicholas W Pino ◽  
Gabriela E Ibarra ◽  
Vishnu Krishnamurthy ◽  
Jefferson Chan

Controlled light-mediated delivery of biological analytes enables the investigation of highly reactivity molecules within cellular systems. As many biological effects are concentration dependent, it is critical to determine the location, time, and quantity of analyte donation. In this work, we have developed the first photoactivatable donor for formaldehyde (FA). Our optimized photoactivatable donor, photoFAD-3, is equipped with a fluorescence readout that enables monitoring of FA release with a concomitant 139-fold fluorescence enhancement. Tuning of photostability and cellular retention enabled quantification of intracellular FA release through cell lysate calibration. Application of photoFAD-3 uncovered the concentration range necessary for arresting wound healing in live cells. This marks the first report where a photoactivatable donor for any analyte has been used to quantify intracellular release.


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