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Optimization of mNeonGreen for Homo sapiens increases its fluorescent intensity in mammalian cells
Green fluorescent protein (GFP) is tremendously useful for investigating many cellular and intracellular events. The monomeric GFP mNeonGreen is about 3- to 5-times brighter than GFP and monomeric enhanced GFP and shows high photostability. The maturation half-time of mNeonGreen is about 3-fold fast...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771595/ https://www.ncbi.nlm.nih.gov/pubmed/29342181 http://dx.doi.org/10.1371/journal.pone.0191108 |
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author | Tanida-Miyake, Emiko Koike, Masato Uchiyama, Yasuo Tanida, Isei |
author_facet | Tanida-Miyake, Emiko Koike, Masato Uchiyama, Yasuo Tanida, Isei |
author_sort | Tanida-Miyake, Emiko |
collection | PubMed |
description | Green fluorescent protein (GFP) is tremendously useful for investigating many cellular and intracellular events. The monomeric GFP mNeonGreen is about 3- to 5-times brighter than GFP and monomeric enhanced GFP and shows high photostability. The maturation half-time of mNeonGreen is about 3-fold faster than that of monomeric enhanced GFP. However, the cDNA sequence encoding mNeonGreen contains some codons that are rarely used in Homo sapiens. For better expression of mNeonGreen in human cells, we synthesized a human-optimized cDNA encoding mNeonGreen and generated an expression plasmid for humanized mNeonGreen under the control of the cytomegalovirus promoter. The resultant plasmid was introduced into HEK293 cells. The fluorescent intensity of humanized mNeonGreen was about 1.4-fold higher than that of the original mNeonGreen. The humanized mNeonGreen with a mitochondria-targeting signal showed mitochondrial distribution of mNeonGreen. We further generated an expression vector of humanized mNeonGreen with 3xFLAG tags at its carboxyl terminus as these tags are useful for immunological analyses. The 3xFLAG-tagged mNeonGreen was recognized well with an anti-FLAG-M2 antibody. These plasmids for the expression of humanized mNeonGreen and mNeonGreen-3xFLAG are useful tools for biological studies in mammalian cells using mNeonGreen. |
format | Online Article Text |
id | pubmed-5771595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-57715952018-01-23 Optimization of mNeonGreen for Homo sapiens increases its fluorescent intensity in mammalian cells Tanida-Miyake, Emiko Koike, Masato Uchiyama, Yasuo Tanida, Isei PLoS One Research Article Green fluorescent protein (GFP) is tremendously useful for investigating many cellular and intracellular events. The monomeric GFP mNeonGreen is about 3- to 5-times brighter than GFP and monomeric enhanced GFP and shows high photostability. The maturation half-time of mNeonGreen is about 3-fold faster than that of monomeric enhanced GFP. However, the cDNA sequence encoding mNeonGreen contains some codons that are rarely used in Homo sapiens. For better expression of mNeonGreen in human cells, we synthesized a human-optimized cDNA encoding mNeonGreen and generated an expression plasmid for humanized mNeonGreen under the control of the cytomegalovirus promoter. The resultant plasmid was introduced into HEK293 cells. The fluorescent intensity of humanized mNeonGreen was about 1.4-fold higher than that of the original mNeonGreen. The humanized mNeonGreen with a mitochondria-targeting signal showed mitochondrial distribution of mNeonGreen. We further generated an expression vector of humanized mNeonGreen with 3xFLAG tags at its carboxyl terminus as these tags are useful for immunological analyses. The 3xFLAG-tagged mNeonGreen was recognized well with an anti-FLAG-M2 antibody. These plasmids for the expression of humanized mNeonGreen and mNeonGreen-3xFLAG are useful tools for biological studies in mammalian cells using mNeonGreen. Public Library of Science 2018-01-17 /pmc/articles/PMC5771595/ /pubmed/29342181 http://dx.doi.org/10.1371/journal.pone.0191108 Text en © 2018 Tanida-Miyake et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Tanida-Miyake, Emiko Koike, Masato Uchiyama, Yasuo Tanida, Isei Optimization of mNeonGreen for Homo sapiens increases its fluorescent intensity in mammalian cells |
title | Optimization of mNeonGreen for Homo sapiens increases its fluorescent intensity in mammalian cells |
title_full | Optimization of mNeonGreen for Homo sapiens increases its fluorescent intensity in mammalian cells |
title_fullStr | Optimization of mNeonGreen for Homo sapiens increases its fluorescent intensity in mammalian cells |
title_full_unstemmed | Optimization of mNeonGreen for Homo sapiens increases its fluorescent intensity in mammalian cells |
title_short | Optimization of mNeonGreen for Homo sapiens increases its fluorescent intensity in mammalian cells |
title_sort | optimization of mneongreen for homo sapiens increases its fluorescent intensity in mammalian cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771595/ https://www.ncbi.nlm.nih.gov/pubmed/29342181 http://dx.doi.org/10.1371/journal.pone.0191108 |
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