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Identification of a nanobody specific to human pulmonary surfactant protein A
Nanobody (Nb) is a promising vector for targeted drug delivery. This study aims to identify an Nb that can specifically target the lung by binding human pulmonary surfactant protein A (SP-A). Human lung frozen tissue sections were used for 3 rounds of biospanning of our previously constructed Nb lib...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431231/ https://www.ncbi.nlm.nih.gov/pubmed/28469136 http://dx.doi.org/10.1038/s41598-017-01456-2 |
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author | He, Xian Wang, Shan-Mei Fang Yin, Zhao Zhao, Meng-Meng Li, Nan Yu, Feng Wang, Liu-Sheng Hu, Yang Du, Yu-Kui Du, Shan-Shan Li, Yan Wei, Ya-Ru Chen, Shan-Shan He, Jian-Hua Weng, Dong Li, Hui-Ping |
author_facet | He, Xian Wang, Shan-Mei Fang Yin, Zhao Zhao, Meng-Meng Li, Nan Yu, Feng Wang, Liu-Sheng Hu, Yang Du, Yu-Kui Du, Shan-Shan Li, Yan Wei, Ya-Ru Chen, Shan-Shan He, Jian-Hua Weng, Dong Li, Hui-Ping |
author_sort | He, Xian |
collection | PubMed |
description | Nanobody (Nb) is a promising vector for targeted drug delivery. This study aims to identify an Nb that can specifically target the lung by binding human pulmonary surfactant protein A (SP-A). Human lung frozen tissue sections were used for 3 rounds of biospanning of our previously constructed Nb library for rat SP-A to establish a sub-library of Nb, which specifically bound human lung tissues. Phage-ELISA was performed to screen the sub-library to identify Nb4, which specifically bound human SP-A. The binding affinity Kd of Nb4 to recombinant human SP-A was 7.48 × 10(−7) M. Nb4 (19 kDa) was stable at 30 °C–37 °C and pH 7.0–7.6 and specifically bound the SP-A in human lung tissue homogenates, human lung A549 cells, and human lung tissues, whereas didn’t react with human liver L-02 cells, kidney 293T cells, and human tissues from organs other than the lung. Nb4 accumulated in the lung of nude mice 5 minutes after a tail vein injection of Nb4 and was excreted 3 hours. Short-term exposure (one month) to Nb4 didn’t cause apparent liver and kidney toxicity in rats, whereas 3-month exposure resulted in mild liver and kidney injuries. Nb4 may be a promising vector to specifically deliver drugs to the lung. |
format | Online Article Text |
id | pubmed-5431231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54312312017-05-16 Identification of a nanobody specific to human pulmonary surfactant protein A He, Xian Wang, Shan-Mei Fang Yin, Zhao Zhao, Meng-Meng Li, Nan Yu, Feng Wang, Liu-Sheng Hu, Yang Du, Yu-Kui Du, Shan-Shan Li, Yan Wei, Ya-Ru Chen, Shan-Shan He, Jian-Hua Weng, Dong Li, Hui-Ping Sci Rep Article Nanobody (Nb) is a promising vector for targeted drug delivery. This study aims to identify an Nb that can specifically target the lung by binding human pulmonary surfactant protein A (SP-A). Human lung frozen tissue sections were used for 3 rounds of biospanning of our previously constructed Nb library for rat SP-A to establish a sub-library of Nb, which specifically bound human lung tissues. Phage-ELISA was performed to screen the sub-library to identify Nb4, which specifically bound human SP-A. The binding affinity Kd of Nb4 to recombinant human SP-A was 7.48 × 10(−7) M. Nb4 (19 kDa) was stable at 30 °C–37 °C and pH 7.0–7.6 and specifically bound the SP-A in human lung tissue homogenates, human lung A549 cells, and human lung tissues, whereas didn’t react with human liver L-02 cells, kidney 293T cells, and human tissues from organs other than the lung. Nb4 accumulated in the lung of nude mice 5 minutes after a tail vein injection of Nb4 and was excreted 3 hours. Short-term exposure (one month) to Nb4 didn’t cause apparent liver and kidney toxicity in rats, whereas 3-month exposure resulted in mild liver and kidney injuries. Nb4 may be a promising vector to specifically deliver drugs to the lung. Nature Publishing Group UK 2017-05-03 /pmc/articles/PMC5431231/ /pubmed/28469136 http://dx.doi.org/10.1038/s41598-017-01456-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article He, Xian Wang, Shan-Mei Fang Yin, Zhao Zhao, Meng-Meng Li, Nan Yu, Feng Wang, Liu-Sheng Hu, Yang Du, Yu-Kui Du, Shan-Shan Li, Yan Wei, Ya-Ru Chen, Shan-Shan He, Jian-Hua Weng, Dong Li, Hui-Ping Identification of a nanobody specific to human pulmonary surfactant protein A |
title | Identification of a nanobody specific to human pulmonary surfactant protein A |
title_full | Identification of a nanobody specific to human pulmonary surfactant protein A |
title_fullStr | Identification of a nanobody specific to human pulmonary surfactant protein A |
title_full_unstemmed | Identification of a nanobody specific to human pulmonary surfactant protein A |
title_short | Identification of a nanobody specific to human pulmonary surfactant protein A |
title_sort | identification of a nanobody specific to human pulmonary surfactant protein a |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431231/ https://www.ncbi.nlm.nih.gov/pubmed/28469136 http://dx.doi.org/10.1038/s41598-017-01456-2 |
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