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Segregation of PIP2 and PIP3 into distinct nanoscale regions within the plasma membrane
PIP(2) and PIP(3) are implicated in a wide variety of cellular signaling pathways at the plasma membrane. We have used STORM imaging to localize clusters of PIP(2) and PIP(3) to distinct nanoscale regions within the plasma membrane of PC12 cells. With anti-phospholipid antibodies directly conjugated...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507238/ https://www.ncbi.nlm.nih.gov/pubmed/23213479 http://dx.doi.org/10.1242/bio.20122071 |
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author | Wang, Jie Richards, David A. |
author_facet | Wang, Jie Richards, David A. |
author_sort | Wang, Jie |
collection | PubMed |
description | PIP(2) and PIP(3) are implicated in a wide variety of cellular signaling pathways at the plasma membrane. We have used STORM imaging to localize clusters of PIP(2) and PIP(3) to distinct nanoscale regions within the plasma membrane of PC12 cells. With anti-phospholipid antibodies directly conjugated with AlexaFluor 647, we found that PIP(2) clusters in membrane domains of 64.5±27.558 nm, while PIP(3) clusters had a size of 125.6±22.408 nm. With two color direct STORM imaging we show that >99% of phospholipid clusters have only one or other phospholipid present. These results indicate that lipid nano-domains can be readily identified using super-resolution imaging techniques, and that the lipid composition and size of clusters is tightly regulated. |
format | Online Article Text |
id | pubmed-3507238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Company of Biologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-35072382012-12-04 Segregation of PIP2 and PIP3 into distinct nanoscale regions within the plasma membrane Wang, Jie Richards, David A. Biol Open Research Article PIP(2) and PIP(3) are implicated in a wide variety of cellular signaling pathways at the plasma membrane. We have used STORM imaging to localize clusters of PIP(2) and PIP(3) to distinct nanoscale regions within the plasma membrane of PC12 cells. With anti-phospholipid antibodies directly conjugated with AlexaFluor 647, we found that PIP(2) clusters in membrane domains of 64.5±27.558 nm, while PIP(3) clusters had a size of 125.6±22.408 nm. With two color direct STORM imaging we show that >99% of phospholipid clusters have only one or other phospholipid present. These results indicate that lipid nano-domains can be readily identified using super-resolution imaging techniques, and that the lipid composition and size of clusters is tightly regulated. The Company of Biologists 2012-07-10 /pmc/articles/PMC3507238/ /pubmed/23213479 http://dx.doi.org/10.1242/bio.20122071 Text en © 2012. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by-nc-sa/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Article Wang, Jie Richards, David A. Segregation of PIP2 and PIP3 into distinct nanoscale regions within the plasma membrane |
title | Segregation of PIP2 and PIP3 into distinct nanoscale regions within the plasma membrane |
title_full | Segregation of PIP2 and PIP3 into distinct nanoscale regions within the plasma membrane |
title_fullStr | Segregation of PIP2 and PIP3 into distinct nanoscale regions within the plasma membrane |
title_full_unstemmed | Segregation of PIP2 and PIP3 into distinct nanoscale regions within the plasma membrane |
title_short | Segregation of PIP2 and PIP3 into distinct nanoscale regions within the plasma membrane |
title_sort | segregation of pip2 and pip3 into distinct nanoscale regions within the plasma membrane |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507238/ https://www.ncbi.nlm.nih.gov/pubmed/23213479 http://dx.doi.org/10.1242/bio.20122071 |
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