Functional Detection of TNF Receptor Family Members by Affinity-Labeled Ligands

Abstract Aberrant expression of TNF family of cytokines has been linked to human diseases, and biologics targeting their signaling have become the best selling drugs globally. However, functional detection with labeled ligands for accurate detection of TNFR family of receptor-expressing target tissu...

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Main Authors: Yang Xu, Lingmo Chang, Anliang Huang, Xiaojun Liu, Xinyu Liu, Hong Zhou, Joshua G. Liang, Peng Liang
Format: Article
Language:English
Published: Nature Publishing Group 2017-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-06343-4
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spelling doaj-4cdf3414717f4446a182075804eda0272020-12-08T00:28:07ZengNature Publishing GroupScientific Reports2045-23222017-07-01711710.1038/s41598-017-06343-4Functional Detection of TNF Receptor Family Members by Affinity-Labeled LigandsYang Xu0Lingmo Chang1Anliang Huang2Xiaojun Liu3Xinyu Liu4Hong Zhou5Joshua G. Liang6Peng Liang7Department of Biochemistry & Molecular Biology, College of Life Sciences, Sichuan UniversityDepartment of Biochemistry & Molecular Biology, College of Life Sciences, Sichuan UniversityLaboratory for Gene and Cell Therapy, Sichuan UniversityDepartment of Biochemistry & Molecular Biology, College of Life Sciences, Sichuan UniversityClover BiopharmaceuticalsDepartment of Biochemistry & Molecular Biology, College of Life Sciences, Sichuan UniversityClover BiopharmaceuticalsDepartment of Biochemistry & Molecular Biology, College of Life Sciences, Sichuan UniversityAbstract Aberrant expression of TNF family of cytokines has been linked to human diseases, and biologics targeting their signaling have become the best selling drugs globally. However, functional detection with labeled ligands for accurate detection of TNFR family of receptor-expressing target tissues or cell types remains to be developed. Here we show that TNF receptor family members are heat-stable and can be recognized both in vitro and in vivo by their ligands labeled with alkaline phosphatase. Such an approach may be used in lieu of antibodies for the identification of the cell types involved in receptor signaling during disease onset and progression.https://doi.org/10.1038/s41598-017-06343-4
collection DOAJ
language English
format Article
sources DOAJ
author Yang Xu
Lingmo Chang
Anliang Huang
Xiaojun Liu
Xinyu Liu
Hong Zhou
Joshua G. Liang
Peng Liang
spellingShingle Yang Xu
Lingmo Chang
Anliang Huang
Xiaojun Liu
Xinyu Liu
Hong Zhou
Joshua G. Liang
Peng Liang
Functional Detection of TNF Receptor Family Members by Affinity-Labeled Ligands
Scientific Reports
author_facet Yang Xu
Lingmo Chang
Anliang Huang
Xiaojun Liu
Xinyu Liu
Hong Zhou
Joshua G. Liang
Peng Liang
author_sort Yang Xu
title Functional Detection of TNF Receptor Family Members by Affinity-Labeled Ligands
title_short Functional Detection of TNF Receptor Family Members by Affinity-Labeled Ligands
title_full Functional Detection of TNF Receptor Family Members by Affinity-Labeled Ligands
title_fullStr Functional Detection of TNF Receptor Family Members by Affinity-Labeled Ligands
title_full_unstemmed Functional Detection of TNF Receptor Family Members by Affinity-Labeled Ligands
title_sort functional detection of tnf receptor family members by affinity-labeled ligands
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-07-01
description Abstract Aberrant expression of TNF family of cytokines has been linked to human diseases, and biologics targeting their signaling have become the best selling drugs globally. However, functional detection with labeled ligands for accurate detection of TNFR family of receptor-expressing target tissues or cell types remains to be developed. Here we show that TNF receptor family members are heat-stable and can be recognized both in vitro and in vivo by their ligands labeled with alkaline phosphatase. Such an approach may be used in lieu of antibodies for the identification of the cell types involved in receptor signaling during disease onset and progression.
url https://doi.org/10.1038/s41598-017-06343-4
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