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Efficient purification and assembly of ribonucleoprotein complex for interaction analysis by MST assay coupled with GaMD simulations

Here, we describe a generic protocol for monitoring protein-RNA interaction using a cleavable GFP fusion of a recombinant RNA-binding protein. We detail each expression and purification step, including high salt and heparin column for contaminant RNA removal. After the assembly of RNA into the ribon...

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Detalles Bibliográficos
Autores principales: Gao, Yunrong, Cao, Dongdong, Pawnikar, Shristi, Akhter, Sana, Miao, Yinglong, Liang, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890042/
https://www.ncbi.nlm.nih.gov/pubmed/33659898
http://dx.doi.org/10.1016/j.xpro.2021.100315
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author Gao, Yunrong
Cao, Dongdong
Pawnikar, Shristi
Akhter, Sana
Miao, Yinglong
Liang, Bo
author_facet Gao, Yunrong
Cao, Dongdong
Pawnikar, Shristi
Akhter, Sana
Miao, Yinglong
Liang, Bo
author_sort Gao, Yunrong
collection PubMed
description Here, we describe a generic protocol for monitoring protein-RNA interaction using a cleavable GFP fusion of a recombinant RNA-binding protein. We detail each expression and purification step, including high salt and heparin column for contaminant RNA removal. After the assembly of RNA into the ribonucleoprotein complex, the MicroScale Thermophoresis assay enables the binding affinity to be obtained quickly with a small amount of sample. Further Gaussian accelerated molecular dynamics simulations allow us to analyze protein:RNA interactions in detail. For complete details on the use and execution of this protocol, please refer to Gao et al. (2020).
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spelling pubmed-78900422021-03-02 Efficient purification and assembly of ribonucleoprotein complex for interaction analysis by MST assay coupled with GaMD simulations Gao, Yunrong Cao, Dongdong Pawnikar, Shristi Akhter, Sana Miao, Yinglong Liang, Bo STAR Protoc Protocol Here, we describe a generic protocol for monitoring protein-RNA interaction using a cleavable GFP fusion of a recombinant RNA-binding protein. We detail each expression and purification step, including high salt and heparin column for contaminant RNA removal. After the assembly of RNA into the ribonucleoprotein complex, the MicroScale Thermophoresis assay enables the binding affinity to be obtained quickly with a small amount of sample. Further Gaussian accelerated molecular dynamics simulations allow us to analyze protein:RNA interactions in detail. For complete details on the use and execution of this protocol, please refer to Gao et al. (2020). Elsevier 2021-02-03 /pmc/articles/PMC7890042/ /pubmed/33659898 http://dx.doi.org/10.1016/j.xpro.2021.100315 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Gao, Yunrong
Cao, Dongdong
Pawnikar, Shristi
Akhter, Sana
Miao, Yinglong
Liang, Bo
Efficient purification and assembly of ribonucleoprotein complex for interaction analysis by MST assay coupled with GaMD simulations
title Efficient purification and assembly of ribonucleoprotein complex for interaction analysis by MST assay coupled with GaMD simulations
title_full Efficient purification and assembly of ribonucleoprotein complex for interaction analysis by MST assay coupled with GaMD simulations
title_fullStr Efficient purification and assembly of ribonucleoprotein complex for interaction analysis by MST assay coupled with GaMD simulations
title_full_unstemmed Efficient purification and assembly of ribonucleoprotein complex for interaction analysis by MST assay coupled with GaMD simulations
title_short Efficient purification and assembly of ribonucleoprotein complex for interaction analysis by MST assay coupled with GaMD simulations
title_sort efficient purification and assembly of ribonucleoprotein complex for interaction analysis by mst assay coupled with gamd simulations
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890042/
https://www.ncbi.nlm.nih.gov/pubmed/33659898
http://dx.doi.org/10.1016/j.xpro.2021.100315
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