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Development of an aptamer-conjugated fluorescent nanoprobe for MMP2

Matrix metalloproteinase 2 (MMP2) plays critical roles in various diseases, such as atherosclerosis and cancer, and has been suggested to contribute to the instability of atherosclerotic plaque. To visualize MMP2 in pathologic tissues, we developed an aptamer targeting MMP2 protein by performing eig...

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Autores principales: Han, Myoung-Eun, Baek, Sungmin, Kim, Hyun-Jung, Lee, Jung Hwan, Ryu, Sung-Ho, Oh, Sae-Ock
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974006/
https://www.ncbi.nlm.nih.gov/pubmed/24589243
http://dx.doi.org/10.1186/1556-276X-9-104
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author Han, Myoung-Eun
Baek, Sungmin
Kim, Hyun-Jung
Lee, Jung Hwan
Ryu, Sung-Ho
Oh, Sae-Ock
author_facet Han, Myoung-Eun
Baek, Sungmin
Kim, Hyun-Jung
Lee, Jung Hwan
Ryu, Sung-Ho
Oh, Sae-Ock
author_sort Han, Myoung-Eun
collection PubMed
description Matrix metalloproteinase 2 (MMP2) plays critical roles in various diseases, such as atherosclerosis and cancer, and has been suggested to contribute to the instability of atherosclerotic plaque. To visualize MMP2 in pathologic tissues, we developed an aptamer targeting MMP2 protein by performing eight rounds of modified DNA systematic evolution of ligands by exponential enrichment (SELEX). The aptamer showed high affinity for MMP2 (K(d) = 5.59 nM), precipitated MMP2, and detected MMP2 protein in pathological tissues such as atherosclerotic plaque and gastric cancer tissues. Furthermore, a MMP2 aptamer-conjugated fluorescent nanoprobe successfully visualized atherosclerotic plaques in apolipoprotein E (ApoE) knockout mice. These results suggest that the devised MMP2 aptamer could be useful for the development of various diagnostic tools.
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spelling pubmed-39740062014-04-17 Development of an aptamer-conjugated fluorescent nanoprobe for MMP2 Han, Myoung-Eun Baek, Sungmin Kim, Hyun-Jung Lee, Jung Hwan Ryu, Sung-Ho Oh, Sae-Ock Nanoscale Res Lett Nano Express Matrix metalloproteinase 2 (MMP2) plays critical roles in various diseases, such as atherosclerosis and cancer, and has been suggested to contribute to the instability of atherosclerotic plaque. To visualize MMP2 in pathologic tissues, we developed an aptamer targeting MMP2 protein by performing eight rounds of modified DNA systematic evolution of ligands by exponential enrichment (SELEX). The aptamer showed high affinity for MMP2 (K(d) = 5.59 nM), precipitated MMP2, and detected MMP2 protein in pathological tissues such as atherosclerotic plaque and gastric cancer tissues. Furthermore, a MMP2 aptamer-conjugated fluorescent nanoprobe successfully visualized atherosclerotic plaques in apolipoprotein E (ApoE) knockout mice. These results suggest that the devised MMP2 aptamer could be useful for the development of various diagnostic tools. Springer 2014-03-03 /pmc/articles/PMC3974006/ /pubmed/24589243 http://dx.doi.org/10.1186/1556-276X-9-104 Text en Copyright © 2014 Han et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Nano Express
Han, Myoung-Eun
Baek, Sungmin
Kim, Hyun-Jung
Lee, Jung Hwan
Ryu, Sung-Ho
Oh, Sae-Ock
Development of an aptamer-conjugated fluorescent nanoprobe for MMP2
title Development of an aptamer-conjugated fluorescent nanoprobe for MMP2
title_full Development of an aptamer-conjugated fluorescent nanoprobe for MMP2
title_fullStr Development of an aptamer-conjugated fluorescent nanoprobe for MMP2
title_full_unstemmed Development of an aptamer-conjugated fluorescent nanoprobe for MMP2
title_short Development of an aptamer-conjugated fluorescent nanoprobe for MMP2
title_sort development of an aptamer-conjugated fluorescent nanoprobe for mmp2
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974006/
https://www.ncbi.nlm.nih.gov/pubmed/24589243
http://dx.doi.org/10.1186/1556-276X-9-104
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