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Agarwala, P.

Publications and source records attributed to Agarwala, P..

2 recordsLinked to original sources

Economical Method to Construct a Prism-based TIRF Setup on an Existing Confocal Microscope to Perform smFRET Experiments

Total internal reflection fluorescence (TIRF) microscopy enables observation of complex bio-assemblies and macromolecular dynamics in high spatial-temporal resolution at single-molecule level in real-time. With TIRF illumination, fluorophores near a sample substrate are excited by an evanescent field, thereby circumventing the axial diffraction limit of light. Prism-based TIRF (p-TIRF) microscopes are comparatively easy to use. They may be readily adjusted to meet the requirements of a broad range of experimental applications, such as to examine of macromolecular complexes, to study of the behaviour of vesicles and small organelles, the study of protein-DNA complexes at the single-molecule level. These experiments can give unique insights into the mechanisms driving the molecular interactions that underline many fundamental activities within the cell by providing information on fluctuation distributions and unusual events. Here, we report a detailed method to build a p-TIRF setup inexpensively using an existing confocal microscope where the same light source can be used for both systems. Furthermore, we provide a brief overview that aims to give the readers a stepwise tutorial protocol for building, assembling, aligning, and preparing the specimen to conduct single-molecule fluorescence resonance energy transfer (smFRET) experiments using a custom-built p-TIRF setup. We believe that this article will be of assistance to labs that already have a confocal microscope and want to perform TIRF experiments for potential future applications. Research HighlightWe report here a simple and cost-effective method to build a prism-based TIRF setup on a laser scanning confocal microscope. The setup is affordable, and users can use both confocal and TIRF modes in the same setup with the same light source and optical components. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=129 SRC="FIGDIR/small/639412v1_ufig1.gif" ALT="Figure 1"> View larger version (25K): org.highwire.dtl.DTLVardef@e476e5org.highwire.dtl.DTLVardef@139d7b8org.highwire.dtl.DTLVardef@81ac21org.highwire.dtl.DTLVardef@14bd8f2_HPS_FORMAT_FIGEXP M_FIG C_FIG

biophysics↗

Enzyme-Regulated Non-Thermal Fluctuations Enhance Ligand Diffusion and Receptor-Mediated Endocytosis

Active enzymes during catalyzing chemical reactions, have been found to generate significant mechanical fluctuations, which can influence the dynamics of their surroundings. These phenomena open new avenues for controlling mass transport in complex and dynamically inhomogeneous environments through localized chemical reactions. To explore this potential, we studied the uptake of transferrin molecules in retinal pigment epithelium (RPE) cells via clathrin-mediated endocytosis. In the presence of enzyme catalysis in the extracellular matrix, we observed a significant enhancement in the transport of fluorophore-tagged transferrin inside the cells. Fluorescence correlation spectroscopy measurements showed substantial increase in transferrin diffusion in the presence of active fluctuations. This study sheds light on the possibility that enzyme-substrate reactions within the extracellular matrix may induce long-range mechanical influences, facilitating targeted material delivery within intracellular milieu more efficiently than passive diffusion. These insights are expected to contribute to the development of better therapeutic strategies by overcoming limitations imposed by slow molecular diffusion under complex environments.

biophysics↗