Cargando…
Bis(sulfosuccinimidyl) suberate (BS(3)) crosslinking analysis of the behavior of amyloid-β peptide in solution and in phospholipid membranes
The structure and state of amyloid-β peptide (Aβ) oligomers often need to be checked by reliable experimental methods. Electrophoresis is a commonly applied measurement method. However, due to the presence of detergents, oligomers are easily broken during electrophoresis, which makes it very hard to...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360245/ https://www.ncbi.nlm.nih.gov/pubmed/28323849 http://dx.doi.org/10.1371/journal.pone.0173871 |
_version_ | 1782516554803445760 |
---|---|
author | Shi, Jing-Ming Pei, Jie Liu, En-Qi Zhang, Lin |
author_facet | Shi, Jing-Ming Pei, Jie Liu, En-Qi Zhang, Lin |
author_sort | Shi, Jing-Ming |
collection | PubMed |
description | The structure and state of amyloid-β peptide (Aβ) oligomers often need to be checked by reliable experimental methods. Electrophoresis is a commonly applied measurement method. However, due to the presence of detergents, oligomers are easily broken during electrophoresis, which makes it very hard to accurately assess Aβ aggregate states. In the current study, bis(sulfosuccinimidyl) suberate (BS(3)) was used to cross-link Aβ1–42 oligomers prior to electrophoresis. When compared to a previously reported Aβ cross-linking agent, glutaraldehyde, it was quite apparent that BS(3) is more suitable for detecting intra-membrane Aβ oligomers and extra-membrane Aβ oligomers states. As such, our findings provide an efficient method for analyzing Aβ proteins or other proteins that are easily aggregated in solution and in phospholipid membranes. |
format | Online Article Text |
id | pubmed-5360245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53602452017-04-06 Bis(sulfosuccinimidyl) suberate (BS(3)) crosslinking analysis of the behavior of amyloid-β peptide in solution and in phospholipid membranes Shi, Jing-Ming Pei, Jie Liu, En-Qi Zhang, Lin PLoS One Research Article The structure and state of amyloid-β peptide (Aβ) oligomers often need to be checked by reliable experimental methods. Electrophoresis is a commonly applied measurement method. However, due to the presence of detergents, oligomers are easily broken during electrophoresis, which makes it very hard to accurately assess Aβ aggregate states. In the current study, bis(sulfosuccinimidyl) suberate (BS(3)) was used to cross-link Aβ1–42 oligomers prior to electrophoresis. When compared to a previously reported Aβ cross-linking agent, glutaraldehyde, it was quite apparent that BS(3) is more suitable for detecting intra-membrane Aβ oligomers and extra-membrane Aβ oligomers states. As such, our findings provide an efficient method for analyzing Aβ proteins or other proteins that are easily aggregated in solution and in phospholipid membranes. Public Library of Science 2017-03-21 /pmc/articles/PMC5360245/ /pubmed/28323849 http://dx.doi.org/10.1371/journal.pone.0173871 Text en © 2017 Shi 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 Shi, Jing-Ming Pei, Jie Liu, En-Qi Zhang, Lin Bis(sulfosuccinimidyl) suberate (BS(3)) crosslinking analysis of the behavior of amyloid-β peptide in solution and in phospholipid membranes |
title | Bis(sulfosuccinimidyl) suberate (BS(3)) crosslinking analysis of the behavior of amyloid-β peptide in solution and in phospholipid membranes |
title_full | Bis(sulfosuccinimidyl) suberate (BS(3)) crosslinking analysis of the behavior of amyloid-β peptide in solution and in phospholipid membranes |
title_fullStr | Bis(sulfosuccinimidyl) suberate (BS(3)) crosslinking analysis of the behavior of amyloid-β peptide in solution and in phospholipid membranes |
title_full_unstemmed | Bis(sulfosuccinimidyl) suberate (BS(3)) crosslinking analysis of the behavior of amyloid-β peptide in solution and in phospholipid membranes |
title_short | Bis(sulfosuccinimidyl) suberate (BS(3)) crosslinking analysis of the behavior of amyloid-β peptide in solution and in phospholipid membranes |
title_sort | bis(sulfosuccinimidyl) suberate (bs(3)) crosslinking analysis of the behavior of amyloid-β peptide in solution and in phospholipid membranes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360245/ https://www.ncbi.nlm.nih.gov/pubmed/28323849 http://dx.doi.org/10.1371/journal.pone.0173871 |
work_keys_str_mv | AT shijingming bissulfosuccinimidylsuberatebs3crosslinkinganalysisofthebehaviorofamyloidbpeptideinsolutionandinphospholipidmembranes AT peijie bissulfosuccinimidylsuberatebs3crosslinkinganalysisofthebehaviorofamyloidbpeptideinsolutionandinphospholipidmembranes AT liuenqi bissulfosuccinimidylsuberatebs3crosslinkinganalysisofthebehaviorofamyloidbpeptideinsolutionandinphospholipidmembranes AT zhanglin bissulfosuccinimidylsuberatebs3crosslinkinganalysisofthebehaviorofamyloidbpeptideinsolutionandinphospholipidmembranes |