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Active and water-soluble form of lipidated Wnt protein is maintained by a serum glycoprotein afamin/α-albumin
Wnt plays important role during development and in various diseases. Because Wnts are lipidated and highly hydrophobic, they can only be purified in the presence of detergents, limiting their use in various in vitro and in vivo assays. We purified N-terminally tagged recombinant Wnt3a secreted from...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4775226/ https://www.ncbi.nlm.nih.gov/pubmed/26902720 http://dx.doi.org/10.7554/eLife.11621 |
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author | Mihara, Emiko Hirai, Hidenori Yamamoto, Hideki Tamura-Kawakami, Keiko Matano, Mami Kikuchi, Akira Sato, Toshiro Takagi, Junichi |
author_facet | Mihara, Emiko Hirai, Hidenori Yamamoto, Hideki Tamura-Kawakami, Keiko Matano, Mami Kikuchi, Akira Sato, Toshiro Takagi, Junichi |
author_sort | Mihara, Emiko |
collection | PubMed |
description | Wnt plays important role during development and in various diseases. Because Wnts are lipidated and highly hydrophobic, they can only be purified in the presence of detergents, limiting their use in various in vitro and in vivo assays. We purified N-terminally tagged recombinant Wnt3a secreted from cells and accidentally discovered that Wnt3a co-purified with a glycoprotein afamin derived from the bovine serum included in the media. Wnt3a forms a 1:1 complex with afamin, which remains soluble in aqueous buffer after isolation, and can induce signaling in various cellular systems including the intestical stem cell growth assay. By co-expressing with afamin, biologically active afamin-Wnt complex can be easily obtained in large quantity. As afamin can also solubilize Wnt5a, Wnt3, and many more Wnt subtypes, afamin complexation will open a way to put various Wnt ligands and their signaling mechanisms under a thorough biochemical scrutiny that had been difficult for years. DOI: http://dx.doi.org/10.7554/eLife.11621.001 |
format | Online Article Text |
id | pubmed-4775226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47752262016-03-07 Active and water-soluble form of lipidated Wnt protein is maintained by a serum glycoprotein afamin/α-albumin Mihara, Emiko Hirai, Hidenori Yamamoto, Hideki Tamura-Kawakami, Keiko Matano, Mami Kikuchi, Akira Sato, Toshiro Takagi, Junichi eLife Biochemistry Wnt plays important role during development and in various diseases. Because Wnts are lipidated and highly hydrophobic, they can only be purified in the presence of detergents, limiting their use in various in vitro and in vivo assays. We purified N-terminally tagged recombinant Wnt3a secreted from cells and accidentally discovered that Wnt3a co-purified with a glycoprotein afamin derived from the bovine serum included in the media. Wnt3a forms a 1:1 complex with afamin, which remains soluble in aqueous buffer after isolation, and can induce signaling in various cellular systems including the intestical stem cell growth assay. By co-expressing with afamin, biologically active afamin-Wnt complex can be easily obtained in large quantity. As afamin can also solubilize Wnt5a, Wnt3, and many more Wnt subtypes, afamin complexation will open a way to put various Wnt ligands and their signaling mechanisms under a thorough biochemical scrutiny that had been difficult for years. DOI: http://dx.doi.org/10.7554/eLife.11621.001 eLife Sciences Publications, Ltd 2016-02-23 /pmc/articles/PMC4775226/ /pubmed/26902720 http://dx.doi.org/10.7554/eLife.11621 Text en © 2016, Mihara et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Mihara, Emiko Hirai, Hidenori Yamamoto, Hideki Tamura-Kawakami, Keiko Matano, Mami Kikuchi, Akira Sato, Toshiro Takagi, Junichi Active and water-soluble form of lipidated Wnt protein is maintained by a serum glycoprotein afamin/α-albumin |
title | Active and water-soluble form of lipidated Wnt protein is maintained by a serum glycoprotein afamin/α-albumin |
title_full | Active and water-soluble form of lipidated Wnt protein is maintained by a serum glycoprotein afamin/α-albumin |
title_fullStr | Active and water-soluble form of lipidated Wnt protein is maintained by a serum glycoprotein afamin/α-albumin |
title_full_unstemmed | Active and water-soluble form of lipidated Wnt protein is maintained by a serum glycoprotein afamin/α-albumin |
title_short | Active and water-soluble form of lipidated Wnt protein is maintained by a serum glycoprotein afamin/α-albumin |
title_sort | active and water-soluble form of lipidated wnt protein is maintained by a serum glycoprotein afamin/α-albumin |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4775226/ https://www.ncbi.nlm.nih.gov/pubmed/26902720 http://dx.doi.org/10.7554/eLife.11621 |
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