Magnetic alignment of rhodamine/magnetite dual-labeled microtubules probed with inverted fluorescence microscopy

Abstract Molecular machines, as exemplified by the kinesin and microtubule system, are responsible for molecular transport in cells. The monitoring of the cellular machinery has attracted much attention in recent years, requiring sophisticated techniques such as optical tweezers, and dark field hyperspectral and fluorescence microscopies. It also demands suitable procedures for immobilization and labeling with functional agents such as dyes, plasmonic nanoparticles and quantum dots. In this work, microtubules were co-polymerized by incubating a tubulin mix consisting of 7 biotinylated tubulin to 3 rhodamine tubulin. Rhodamine provided the fluorescent tag, while biotin was the anchoring group for receiving streptavidin containing species. To control the microtubule alignment and consequently, the molecular gliding directions, functionalized iron oxide nanoparticles were employed in the presence of an external magnet field. Such iron oxide nanoparticles, (MagNPs) were previously coated with silica and (3-aminopro-pyl)triethoxysilane (APTS) and then modified with streptavidin (SA) for linking to the biotin-functionalized microtubules. In this way, the binding has been successfully performed, and the magnetic alignment probed by Inverted Fluorescence Microscopy. The proposed strategy has proved promising, as tested with one of the most important biological structures of the cellular machinery.

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Main Authors: TOMA,HENRIQUE EISI, OLIVEIRA,DANIEL, MELO,FERNANDO M. DE
Format: Digital revista
Language:English
Published: Academia Brasileira de Ciências 2022
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652022000500502
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spelling oai:scielo:S0001-376520220005005022022-07-28Magnetic alignment of rhodamine/magnetite dual-labeled microtubules probed with inverted fluorescence microscopyTOMA,HENRIQUE EISIOLIVEIRA,DANIELMELO,FERNANDO M. DE Molecular machines kinesin and microtubules magnetic nanoparticles fluorescence microscopy CytoViva hypermicroscopy Abstract Molecular machines, as exemplified by the kinesin and microtubule system, are responsible for molecular transport in cells. The monitoring of the cellular machinery has attracted much attention in recent years, requiring sophisticated techniques such as optical tweezers, and dark field hyperspectral and fluorescence microscopies. It also demands suitable procedures for immobilization and labeling with functional agents such as dyes, plasmonic nanoparticles and quantum dots. In this work, microtubules were co-polymerized by incubating a tubulin mix consisting of 7 biotinylated tubulin to 3 rhodamine tubulin. Rhodamine provided the fluorescent tag, while biotin was the anchoring group for receiving streptavidin containing species. To control the microtubule alignment and consequently, the molecular gliding directions, functionalized iron oxide nanoparticles were employed in the presence of an external magnet field. Such iron oxide nanoparticles, (MagNPs) were previously coated with silica and (3-aminopro-pyl)triethoxysilane (APTS) and then modified with streptavidin (SA) for linking to the biotin-functionalized microtubules. In this way, the binding has been successfully performed, and the magnetic alignment probed by Inverted Fluorescence Microscopy. The proposed strategy has proved promising, as tested with one of the most important biological structures of the cellular machinery.info:eu-repo/semantics/openAccessAcademia Brasileira de CiênciasAnais da Academia Brasileira de Ciências v.94 n.3 20222022-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652022000500502en10.1590/0001-3765202220210917
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
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region America del Sur
libraryname SciELO
language English
format Digital
author TOMA,HENRIQUE EISI
OLIVEIRA,DANIEL
MELO,FERNANDO M. DE
spellingShingle TOMA,HENRIQUE EISI
OLIVEIRA,DANIEL
MELO,FERNANDO M. DE
Magnetic alignment of rhodamine/magnetite dual-labeled microtubules probed with inverted fluorescence microscopy
author_facet TOMA,HENRIQUE EISI
OLIVEIRA,DANIEL
MELO,FERNANDO M. DE
author_sort TOMA,HENRIQUE EISI
title Magnetic alignment of rhodamine/magnetite dual-labeled microtubules probed with inverted fluorescence microscopy
title_short Magnetic alignment of rhodamine/magnetite dual-labeled microtubules probed with inverted fluorescence microscopy
title_full Magnetic alignment of rhodamine/magnetite dual-labeled microtubules probed with inverted fluorescence microscopy
title_fullStr Magnetic alignment of rhodamine/magnetite dual-labeled microtubules probed with inverted fluorescence microscopy
title_full_unstemmed Magnetic alignment of rhodamine/magnetite dual-labeled microtubules probed with inverted fluorescence microscopy
title_sort magnetic alignment of rhodamine/magnetite dual-labeled microtubules probed with inverted fluorescence microscopy
description Abstract Molecular machines, as exemplified by the kinesin and microtubule system, are responsible for molecular transport in cells. The monitoring of the cellular machinery has attracted much attention in recent years, requiring sophisticated techniques such as optical tweezers, and dark field hyperspectral and fluorescence microscopies. It also demands suitable procedures for immobilization and labeling with functional agents such as dyes, plasmonic nanoparticles and quantum dots. In this work, microtubules were co-polymerized by incubating a tubulin mix consisting of 7 biotinylated tubulin to 3 rhodamine tubulin. Rhodamine provided the fluorescent tag, while biotin was the anchoring group for receiving streptavidin containing species. To control the microtubule alignment and consequently, the molecular gliding directions, functionalized iron oxide nanoparticles were employed in the presence of an external magnet field. Such iron oxide nanoparticles, (MagNPs) were previously coated with silica and (3-aminopro-pyl)triethoxysilane (APTS) and then modified with streptavidin (SA) for linking to the biotin-functionalized microtubules. In this way, the binding has been successfully performed, and the magnetic alignment probed by Inverted Fluorescence Microscopy. The proposed strategy has proved promising, as tested with one of the most important biological structures of the cellular machinery.
publisher Academia Brasileira de Ciências
publishDate 2022
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652022000500502
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AT oliveiradaniel magneticalignmentofrhodaminemagnetiteduallabeledmicrotubulesprobedwithinvertedfluorescencemicroscopy
AT melofernandomde magneticalignmentofrhodaminemagnetiteduallabeledmicrotubulesprobedwithinvertedfluorescencemicroscopy
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