Investigating Spatial Heterogeneity of Nanoparticles Movement in Live Cells with Pair-Correlation Microscopy and Phasor Analysis

2021 ◽  
Vol 93 (8) ◽  
pp. 3803-3812
Author(s):  
Wenqian Wang ◽  
Yuanqing Ma ◽  
Simone Bonaccorsi ◽  
Vu Thanh Cong ◽  
Elvis Pandžić ◽  
...  
2020 ◽  
Vol 1 (2) ◽  
Author(s):  
Leonel Malacrida ◽  
Per Niklas Hedde ◽  
Belen Torrado ◽  
Enrico Gratton

ABSTRACT Transient barriers are fundamental to cell supramolecular organization and assembly. Discontinuities between spaces can be generated by a physical barrier but also by thermodynamic barriers achieved by phase separation of molecules. However, because of the transient nature and the lack of a visible barrier, the existence of phase separation is difficult to demonstrate experimentally. We describe an approach based on the 2-dimensional pair correlation function (2D-pCF) analysis of the spatial connectivity in a cell. The educational aim of the article is to present both a model suitable for explaining diffusion barrier measurements to a broad range of courses and examples of biological situations. If there are no barriers to diffusion, particles could diffuse equally in all directions. In this situation the pair correlation function introduced in this article is independent of the direction and is uniform in all directions. However, in the presence of obstacles, the shape of the 2D-pCF is distorted to reflect how the obstacle position and orientation change the flow of molecules. In the example shown in this article, measurements of diffusion of enhanced green fluorescent protein moving in live cells show the lack of connectivity at the nucleolus surface for shorter distances. We also observe a gradual increase in the connectivity for longer distances or times, presumably because of molecular trajectories around the nucleolus.


2016 ◽  
Vol 12 (1) ◽  
pp. 81-89 ◽  
Author(s):  
Elizabeth Hinde ◽  
Kitiphume Thammasiraphop ◽  
Hien T. T. Duong ◽  
Jonathan Yeow ◽  
Bunyamin Karagoz ◽  
...  

2018 ◽  
Vol 114 (3) ◽  
pp. 166a
Author(s):  
Leonel S. Malacrida ◽  
Per Niklas Hedde ◽  
Suman Ranjit ◽  
Francesco Cardarelli ◽  
Enrico Gratton

Author(s):  
Shinya Inoué

This paper reports progress of our effort to rapidly capture, and display in time-lapsed mode, the 3-dimensional dynamic architecture of active living cells and developing embryos at the highest resolution of the light microscope. Our approach entails: (A) real-time video tape recording of through-focal, ultrathin optical sections of live cells at the highest resolution of the light microscope; (B) repeat of A at time-lapsed intervals; (C) once each time-lapsed interval, an image at home focus is recorded onto Optical Disk Memory Recorder (OMDR); (D) periods of interest are selected using the OMDR and video tape records; (E) selected stacks of optical sections are converted into plane projections representing different view angles (±4 degrees for stereo view, additional angles when revolving stereos are desired); (F) analysis using A - D.


Author(s):  
E. D. Salmon ◽  
J. C. Waters ◽  
C. Waterman-Storer

We have developed a multi-mode digital imaging system which acquires images with a cooled CCD camera (Figure 1). A multiple band pass dichromatic mirror and robotically controlled filter wheels provide wavelength selection for epi-fluorescence. Shutters select illumination either by epi-fluorescence or by transmitted light for phase contrast or DIC. Many of our experiments involve investigations of spindle assembly dynamics and chromosome movements in live cells or unfixed reconstituted preparations in vitro in which photodamage and phototoxicity are major concerns. As a consequence, a major factor in the design was optical efficiency: achieving the highest image quality with the least number of illumination photons. This principle applies to both epi-fluorescence and transmitted light imaging modes. In living cells and extracts, microtubules are visualized using X-rhodamine labeled tubulin. Photoactivation of C2CF-fluorescein labeled tubulin is used to locally mark microtubules in studies of microtubule dynamics and translocation. Chromosomes are labeled with DAPI or Hoechst DNA intercalating dyes.


Author(s):  
K.I. Pagh ◽  
M.R. Adelman

Unicellular amoebae of the slime mold Physarum polycephalum undergo marked changes in cell shape and motility during their conversion into flagellate swimming cells (l). To understand the processes underlying motile activities expressed during the amoebo-flagellate transformation, we have undertaken detailed investigations of the organization, formation and functions of subcellular structures or domains of the cell which are hypothesized to play a role in movement. One focus of our studies is on a structure, termed the “ridge” which appears as a flattened extension of the periphery along the length of transforming cells (Fig. 1). Observations of live cells using Nomarski optics reveal two types of movement in this region:propagation of undulations along the length of the ridge and formation and retraction of filopodial projections from its edge. The differing activities appear to be associated with two characteristic morphologies, illustrated in Fig. 1.


2015 ◽  
Vol 2 (1) ◽  
pp. 50-59
Author(s):  
V. Medvedev

Aim. To consider soil continuality and discreteness as features of heterogeneity manifestation in a soil cover, important for construction of agriculture systems. Methods. Geostatistical research of soil spatial heterogeneity, revealing the contours of a fi eld with various parameters of fertility. Results. The use of principles of precise agriculture and inspection of indicative properties of fi eld soils using a regular grid allowed to divide a fi eld into contours with three levels of fertility: the fi rst one is characterized by optimal or close to optimum properties which allows refusing from (or reducing substantially) tillage, introduction of fertilizers or chemical ameliorates; the second one has average parameters of fertility corresponding to zonal soils and demands the application of zonal technologies; the third one (with the worst parameters of fertility) presupposes regular use of the improved technologies. Conclusions. The introduction of precise agriculture will allow replacing a traditional zonal system with thenew which is soil-protecting and resource-saving one.


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