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Gotowe bibliografie tematyczne / Protein Dynamics - Confocal Microscopy

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Gotowa bibliografia na temat „Protein Dynamics - Confocal Microscopy”

Autor: Grafiati

Data publikacji: 7 września 2023

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Rozprawy doktorskie na temat "Protein Dynamics - Confocal Microscopy"

1

Nilufar, Rahimova. "Real-time dynamics of IκBαdegradation studied with Kusabira-Orange 2 fusion proteins". 京都大学 (Kyoto University), 2016. http://hdl.handle.net/2433/217147.

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Gösch, Michael. "Microfluidic analysis and parallel confocal detection of single molecules /." Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-663-4/.

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Piguet, Joachim. "Advanced Fluorescence Microscopy to Study Plasma Membrane Protein Dynamics." Doctoral thesis, Ecole Polytechnique Fédérale de Lausanne (EPFL), Switzerland, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-178147.

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Membrane protein dynamics is of great importance for living organisms. The precise localization of proteins composing a synapse on the membrane facing a nerve terminus is essential for proper functioning of the nervous system. In muscle fibers, the nicotinic acetylcholine is densely packed under the motor nerve termini. A receptor associated protein, rapsyn, acts as a linker between the receptor and the other components of the synaptic suramolecular assembly. Advances in fluorescence microscopy have allowed to measure the behavior of a single receptor in the cell membrane. In this work single-

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Elmlund, Hans. "Protein structure dynamics and interplay : by single-particle electron microscopy." Doctoral thesis, Stockholm : Teknik och hälsa, Technology and Health, Kungliga Tekniska högskolan, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4669.

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5

Guo, Qing. "Single Molecule Optical Magnetic Tweezers Microscopy Studies of Protein Dynamics." Bowling Green State University / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1435334948.

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SCIPIONI, LORENZO. "Local image correlation methods for the characterization of subcellular structure and dynamics by confocal and super-resolution microscopy." Doctoral thesis, Università degli studi di Genova, 2018. http://hdl.handle.net/11567/929279.

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This thesis work aspires to present a new concept for the application of correlation techniques to the study of the cellular environment. By exploiting local analysis in combination to a fast fit-free technique (the phasor approach) we provide an exhaustive high-resolution analysis of structural and dynamic properties while maintaining a reasonable computation time. The dissertation will be articulated as follows: In CHAPTER 1 we aim to provide the reader with a description of the techniques that will be exploited during the rest of the dissertation together with the open questions and proble

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Vallejo, Rodriguez Johana. "Compartmentation of glycolysis to a plasma membrane domain : role of caveolin-1 as a scaffolding protein for phosphofructokinase /." Free to MU Campus, others may purchase, 2004. http://wwwlib.umi.com/cr/mo/fullcit?p3137759.

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Ljunglöf, Anders. "Direct observation of biomolecule adsorption and spatial distribution of functional groups in chromatographic adsorbent particles." Doctoral thesis, Uppsala University, Surface Biotechnology, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1602.

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<p>Confocal microscopy has been used as a tool for studying adsorption of biomolecules to individual chromatographic adsorbent particles. By coupling a fluorescent dye to protein molecules, their penetration into single adsorbent particles could be observed visually at different times during batch uptake. By relating the relative fluorescence intensity obtained at different times to the value at equilibrium, the degree of saturation versus time could be constructed. The use of two different fluorescent dyes for protein labeling and two independent detectors, allowed direct observation of a two

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des, Georges Amédée. "Regulation of tubulin dynamics by the +Tip tracking protein Mal3." Thesis, University of Cambridge, 2008. https://www.repository.cam.ac.uk/handle/1810/256531.

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The Microtubule (MT) network is a central component of the eukaryotic cell cytoskeleton. In the fission yeast S. pombe, a complex of three proteins specifically tracks MT +ends and stabilizes MTs in the cell. It is composed of the proteins Mal3, Tip1 and Tea2. Mal3, the S. pombe homologue of EB1, is a highly conserved ubiquitous protein found to be at the centre of many MT related processes. Tip1 is a CLIP170 homologue and Tea2 a kinesin-like motor protein. The mechanism by which they target the growing end of MTs and stabilize them is still unknown. A combination of biochemistry, electron mic

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Roy, Chowdhury Susovan. "Single-Molecule Force Manipulation and Nanoscopic Imaging of Protein Structure-Dynamics-Function Relationship." Bowling Green State University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu162707900722617.

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