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Development of a method for screening short-lived proteins using green fluorescent protein
We have developed a screening technology for the identification of short-lived proteins. A green fluorescent protein (GFP)-fusion cDNA library was generated for monitoring degradation kinetics. Cells expressing a subset of the GFP-cDNA expression library were screened to recover those in which the f...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC545601/ https://www.ncbi.nlm.nih.gov/pubmed/15461799 http://dx.doi.org/10.1186/gb-2004-5-10-r81 |
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author | Jiang, Xin Coffino, Philip Li, Xianqiang |
author_facet | Jiang, Xin Coffino, Philip Li, Xianqiang |
author_sort | Jiang, Xin |
collection | PubMed |
description | We have developed a screening technology for the identification of short-lived proteins. A green fluorescent protein (GFP)-fusion cDNA library was generated for monitoring degradation kinetics. Cells expressing a subset of the GFP-cDNA expression library were screened to recover those in which the fluorescence signal diminished rapidly when protein synthesis was inhibited. Thirty clones that met the screening criteria were characterized individually. Twenty-three (73%) proved to have a half-life of 4 hours or less. |
format | Text |
id | pubmed-545601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5456012005-01-26 Development of a method for screening short-lived proteins using green fluorescent protein Jiang, Xin Coffino, Philip Li, Xianqiang Genome Biol Method We have developed a screening technology for the identification of short-lived proteins. A green fluorescent protein (GFP)-fusion cDNA library was generated for monitoring degradation kinetics. Cells expressing a subset of the GFP-cDNA expression library were screened to recover those in which the fluorescence signal diminished rapidly when protein synthesis was inhibited. Thirty clones that met the screening criteria were characterized individually. Twenty-three (73%) proved to have a half-life of 4 hours or less. BioMed Central 2004 2004-09-28 /pmc/articles/PMC545601/ /pubmed/15461799 http://dx.doi.org/10.1186/gb-2004-5-10-r81 Text en Copyright © 2004 Jiang et al.; licensee BioMed Central Ltd. |
spellingShingle | Method Jiang, Xin Coffino, Philip Li, Xianqiang Development of a method for screening short-lived proteins using green fluorescent protein |
title | Development of a method for screening short-lived proteins using green fluorescent protein |
title_full | Development of a method for screening short-lived proteins using green fluorescent protein |
title_fullStr | Development of a method for screening short-lived proteins using green fluorescent protein |
title_full_unstemmed | Development of a method for screening short-lived proteins using green fluorescent protein |
title_short | Development of a method for screening short-lived proteins using green fluorescent protein |
title_sort | development of a method for screening short-lived proteins using green fluorescent protein |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC545601/ https://www.ncbi.nlm.nih.gov/pubmed/15461799 http://dx.doi.org/10.1186/gb-2004-5-10-r81 |
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