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Measuring Cellular Mechanics with Quantitative Phase Microscopy

Measuring Cellular Mechanics with Quantitative Phase Microscopy
Author: Thang Le Nguyen
Publisher:
Total Pages: 421
Release: 2022
Genre:
ISBN:

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Quantitative phase imaging (QPI) is a label-free microscopy approach using the phase shift of light as it passes through transparent objects, like mammalian cells, to quantify biomass distribution and changes in biomass over time and space. QPI has seen immense interest and advances in hardware and software leading to numerous applications in biology and expansions in utility within the last decades. This dissertation presents a subset of those studies applied to questions of cellular biology and biophysics along with an overview of the QPI field as whole. The initial proportion of this thesis is devoted to modeling and dissecting various biomechanical properties of cellular mechanics including cellular viscoelasticity and work across varying cell types and biological perturbations using purely QPI. This is followed by an in-depth review of the field of QPI including the development and lineages of the various QPI approaches along with the advances in QPI made in the field of cellular biology, biophysics, and diagnostics. Finally, we conclude this thesis with a review of the ongoing technical and biological advances made in QPI along with perspectives on the directions that QPI field maybe proceeding towards. Demonstrating that QPI is not only a robust tool in probing cellular biology and biophysics already but is also expanding its' capabilities towards more applications in and interrogating fundamental questions about biology.


Measuring Cell Mechanics

Measuring Cell Mechanics
Author: Margaret Gardel
Publisher: Biota Publishing
Total Pages: 77
Release: 2015-09-01
Genre: Science
ISBN: 1615046992

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Cells are inherently physical entities that both experience mechanical forces from their external environment and generate their own internal forces to drive cell motion. Our particular aim here is to present the reader with an introduction to the primary tools used to measure these mechanical interactions and the material properties of cells that result from them. These approaches can be applied to a diverse array of physiological processes and systems, providing important insight into the regulatory roles of mechanical interactions in cells. We cover techniques at both the molecular and cellular scales, including those that actively and passively probe the system. Along the way we cover the fundamental principles of each approach, while emphasizing the relevant length and timescales, along with the typical magnitudes of the measurements that can be made. Each section ends by highlighting uses of the various techniques in recent relevant publications, illustrating the exciting future of cell mechanics in quantitative cell biology research.


Quantitative Phase Imaging of Cells and Tissues

Quantitative Phase Imaging of Cells and Tissues
Author: Gabriel Popescu
Publisher: McGraw Hill Professional
Total Pages: 384
Release: 2011-03-14
Genre: Technology & Engineering
ISBN: 0071663436

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Cutting-edge quantitative phase imaging techniques and their applications Filled with unique, full-color images taken by advanced quantitative phase imaging (QPI), Quantitative Phase Imaging of Cells and Tissues thoroughly explores this innovative technology and its biomedical applications. An introductory background on optical imaging and traditional optical microscopy is included to illustrate concept development. The book explains how various visualization modalities can be obtained by numerical calculations. This authoritative resource reveals how to take full advantage of the unprecedented capabilities of QPI, such as rendering scattering properties of minute subcellular structures and nanoscale fluctuations in live cells. Coverage includes: Groundwork Spatiotemporal field correlations Image characteristics Light microscopy Holography Point scanning QPI methods Principles of full-field QPI Off-axis full-field methods Phase-shifting techniques Common-path methods White light techniques Fourier transform light scattering (FTLS) Current trends in QPI


Biomedical Optical Phase Microscopy and Nanoscopy

Biomedical Optical Phase Microscopy and Nanoscopy
Author: Natan T. Shaked
Publisher: Academic Press
Total Pages: 428
Release: 2012-11-05
Genre: Medical
ISBN: 0124158714

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Written by leading optical phase microscopy experts, this book is a comprehensive reference to phase microscopy and nanoscopy techniques for biomedical applications, including differential interference contrast (DIC) microscopy, phase contrast microscopy, digital holographic microscopy, optical coherence tomography, tomographic phase microscopy, spectral-domain phase detection, and nanoparticle usage for phase nanoscopy The Editors show biomedical and optical engineers how to use phase microscopy for visualizing unstained specimens, and support the theoretical coverage with applied content and examples on designing systems and interpreting results in bio- and nanoscience applications. Provides a comprehensive overview of the principles and techniques of optical phase microscopy and nanoscopy with biomedical applications. Tips/advice on building systems and working with advanced imaging biomedical techniques, including interpretation of phase images, and techniques for quantitative analysis based on phase microscopy. Interdisciplinary approach that combines optical engineering, nanotechnology, biology and medical aspects of this topic. Each chapter includes practical implementations and worked examples.


Near-infrared Quantitative Phase Imaging of Cellular Manipulation Under Different Physio-chemical Environments

Near-infrared Quantitative Phase Imaging of Cellular Manipulation Under Different Physio-chemical Environments
Author: Bipin Joshi
Publisher:
Total Pages:
Release: 2014
Genre:
ISBN:

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Quantitative phase imaging using Digital Holographic Microscopy (DHM) is emergine as a label-free and wide-field method of characterizing cells with high spatio-temporal resolution. In parallel, silicon based michromechanical and electronic devices are allowing both manipulation (e.g. electrical stimulation, mechanical actuation) as well as characterization (electrical and mechanical) of micro and nano-scopic samples. THis has revolutionized development of lab-on-a-chip devices for high throughput analysis of cells and molecules for diagnosis of disease and screening of drug-effects. However, very little progress has been made in optical (e.g. fluorescence, Raman etc) characterization of samples on these silicon-based devices. Especially, wide-field high-resolution optical imaging and characterization of samples under silicon environment has not been possible owing to the opacity of silicon to visible light. This thesis reports high resolution near-infrared quantitative phase imaging of cells through silicon, in isotonic as well as hypotonic environment using DHM. Further, several microscopic (AFM, laser manipulation) methods are being developed for characterization of mechanical properties (e.g. elasticity) of cells so as to determine changes during physiological stress. In particular, optical tweezers are used for transverse-stretching cells by actuating anchored-beads as handles and imaging using phase-contrast microscopy. While this method is constantly gaining more attention due to non-contact nature of actuation, it is very time consuming and has low working distance. The thesis describes development of a weakly-focused laser beam for axial-stretching. Application of DHM allowed cell imaging with nm-resolution when stretched axially. Development of an empirical formula for force exerted by defocused light beam on a cell surface led to measurement of elastic property of cell. In addition to this, the thesis aimed at evaluating changes in elastic properties of cell under over-expression of certain proteins (HOX-B9), which is believed to be involved in tumorigenesis. Significant reduction in elastic property of cells over-expressing HOXB9 was found as compared to the control cells. Thus, the thesis paves the way for development of a method for optical manipulation and imaging of cells for characterization of their elastic properties in different physiological states, and probe nanoscale interatctions with different physio-chemical agents in a non-invasis and label-free manner.


Quantitative Imaging in Cell Biology

Quantitative Imaging in Cell Biology
Author:
Publisher: Academic Press
Total Pages: 609
Release: 2014-06-25
Genre: Science
ISBN: 0124202012

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This new volume, number 123, of Methods in Cell Biology looks at methods for quantitative imaging in cell biology. It covers both theoretical and practical aspects of using optical fluorescence microscopy and image analysis techniques for quantitative applications. The introductory chapters cover fundamental concepts and techniques important for obtaining accurate and precise quantitative data from imaging systems. These chapters address how choice of microscope, fluorophores, and digital detector impact the quality of quantitative data, and include step-by-step protocols for capturing and analyzing quantitative images. Common quantitative applications, including co-localization, ratiometric imaging, and counting molecules, are covered in detail. Practical chapters cover topics critical to getting the most out of your imaging system, from microscope maintenance to creating standardized samples for measuring resolution. Later chapters cover recent advances in quantitative imaging techniques, including super-resolution and light sheet microscopy. With cutting-edge material, this comprehensive collection is intended to guide researchers for years to come. Covers sections on model systems and functional studies, imaging-based approaches and emerging studies Chapters are written by experts in the field Cutting-edge material


Quantitative Phase Microscopy for the Study of Electromotility in Living Cells

Quantitative Phase Microscopy for the Study of Electromotility in Living Cells
Author: Seungeun Oh
Publisher:
Total Pages: 123
Release: 2010
Genre:
ISBN:

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The electric activity of living cells is accompanied with changes in their optical and mechanical properties, which arise from the intrinsic biophysics of the cell membrane. These intrinsic changes can be used as an indicator for cell electric activity, but, to our knowledge, the intrinsic signal of electric activity has never been detected in single vertebrate cells. We describe here our development of a quantitative phase microscopy technique that is capable of detecting the intrinsic changes induced by electric activity in a human cell line. Chapter 1 provides introductory material regarding cellular electrophysiology and a review of the literature on the intrinsic signal of cell electric activity. This chapter also briefly introduces the quantitative phase microscope. In Chapter 2, we discuss our pilot studies and introduce the electromotility of prestinexpressing HEK293 cells as a test system. We describe our design of an effective optical detection scheme based on quantitative phase imaging and frequency domain detection which provides full-field, high resolution, high sensitivity, quantitative detection of electrically induced optical signals in cells. In Chapter 3, we demonstrate an improved quantitative phase microscope based on low-coherence interferometry with enhanced sensitivity and lower noise. We successfully acquired images of the intrinsic optical signal from electrically stimulated single HEK293 cells. In Chapter 4, we characterized the electrochemical properties and dynamic properties of the intrinsic optical signal. We argue that the signal is generated through the electromechanical coupling mechanism called membrane electromotility (MEM). Using the MEM signal as an indicator of membrane electric activity, we imaged the propagation of an applied potential in a network of cells in Chapter 5. Our research shows that high resolution quantitative phase imaging is a powerful tool that can provide significant insight into the underlying mechanism of cellular intrinsic optical signal of electric activity. Membrane electromotility imaging provides a novel opportunity for the visualization of the electrical connectivity of cultured cells.


Quantitative Phase Imaging

Quantitative Phase Imaging
Author: Gabriel Popescu
Publisher:
Total Pages:
Release: 2015
Genre: Diagnostic imaging
ISBN:

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'Proceedings of SPIE' presents the original research papers presented at SPIE conferences and other high-quality conferences in the broad-ranging fields of optics and photonics. These books provide prompt access to the latest innovations in research and technology in their respective fields.


Study of the Motility of Biological Cells by Digital Holographic Microscopy

Study of the Motility of Biological Cells by Digital Holographic Microscopy
Author: Xiao Yu
Publisher:
Total Pages:
Release: 2014
Genre:
ISBN:

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In this dissertation, I utilize digital holographic microscopy (DHM) to study the motility of biological cells. As an important feature of DHM, quantitative phase microscopy by digital holography (DH-QPM) is applied to study the cell-substrate interactions and migratory behavior of adhesive cells. The traction force exerted by biological cells is visualized as distortions in flexible substrata. Motile fibroblasts produce wrinkles when attached to a silicone rubber film. For the non-wrinkling elastic substrate polyacrylamide (PAA), surface deformation due to fibroblast adhesion and motility is visualized as tangential and vertical displacement. This surface deformation and the associated cellular traction forces are measured from phase profiles based on the degree of distortion. Intracellular fluctuations in amoeba cells are also analyzed statistically by DH-QPM. With the capacity of yielding quantitative measures directly, DH-QPM provides efficient and versatile means for quantitative analysis of cellular or intracellular motility. Three-dimensional profiling and tracking by DHM enable label-free and quantitative analysis of the characteristics and dynamic processes of objects, since DHM can record real-time data for micro-scale objects and produce a single hologram containing all the information about their three-dimensional structure. Here, I utilize DHM to visualize suspended microspheres and microfibers in three dimensions, and record the four-dimensional trajectories of free-swimming cells in the absence of mechanical focus adjustment. The displacement of microfibers due to interactions with cells in three spatial dimensions is measured as a function of time at sub-second and micrometer levels in a direct and straightforward manner. It has thus been shown that DHM is a highly efficient and versatile means for quantitative tracking and analysis of cell motility.