题名 | Novel EBV LMP1 C-terminal domain binding affibody molecules as potential agents for in vivo molecular imaging diagnosis of nasopharyngeal carcinoma |
作者 | |
发表日期 | 2021-10 |
发表期刊 | APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | Affibody molecules EBV LMP1 Nasopharyngeal carcinoma Molecular imaging |
其他关键词 | EPSTEIN-BARR-VIRUS ; EXPRESSION ; PROTEINS |
摘要 | Nasopharyngeal carcinoma (NPC) is consistently associated with Epstein-Barr virus (EBV) latent infection and is common in Southern China and Southeast Asia. The viral latent membrane proteins LMP1 and LMP2 are persistently expressed in NPC tissues; the cytoplasmic domain of LMP1 (LMP1 C-terminal) and LMP2A (LMP2A N-terminal) proteins is essential for maintenance of latency and can alter host cell signaling to facilitate tumor growth and progression. Thus, targeting LMP1 or LMP2 oncoprotein has been an increasing interest for diagnosis and targeted therapy of NPC. Affibody molecules, a new class of small-affinity engineered scaffold proteins, have demonstrated high potential for therapeutics, diagnostics, and biotechnological applications. More recently, radiolabelled HER2-specific affibody molecules have demonstrated to be useful in imaging of HER2 expressing tumor. In this study, we report three novel EBV LMP1 C-terminal (EBV LMP1-C) domain affibody molecules (Z(LMP1-C)15, Z(LMP1-C)114, and Z(LMP1-C)277) were selected by biopanning from a random-peptide displayed phage library and used for molecular imaging in tumor-bearing nude mice. Surface plasmon resonance (SPR), indirect immunofluorescence, and immunohistochemistry (IHC) clearly showed that all three selected affibody molecules have high affinity and specificity in binding to EBV LMP1 protein. Moreover, in vivo tumor imaging revealed that Dylight-755-labeled affibody molecules accumulated rapidly in tumor site after injection (1 h) and then were continuously maintained for 24 h in EBV-positive NPC xenograft mice model. In conclusion, our findings highlight the potential use of Z(LMP1-C) affibody molecules as tumor-specific molecular imaging agents of EBV-associated NPC. |
资助项目 | National Nature Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81972550, 81372447] |
出版者 | SPRINGER |
出版地 | NEW YORK |
ISSN | 0175-7598 |
EISSN | 1432-0614 |
卷号 | 105期号:19页码:7283-7293 |
DOI | 10.1007/s00253-021-11559-6 |
页数 | 36 |
WOS类目 | Biotechnology & Applied Microbiology |
WOS研究方向 | Biotechnology & Applied Microbiology |
WOS记录号 | WOS:000694774600002 |
收录类别 | SCIE ; PUBMED ; EI ; SCOPUS |
EI入藏号 | 20213710888330 |
EI主题词 | Molecular imaging |
URL | 查看原文 |
PubMed ID | 34505914 |
SCOPUSEID | 2-s2.0-85114686875 |
通讯作者地址 | [Zhang, Lifang]Institute of Molecular Virology and Immunology,Department of Microbiology and Immunology,School of Basic Medical Sciences,Wenzhou Medical University,Wenzhou,325035,China |
Scopus学科分类 | Biotechnology;Applied Microbiology and Biotechnology |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/14443 |
专题 | 基础医学院(机能实验教学中心)_病原生物学与免疫学系 |
通讯作者 | Zhang, Lifang |
作者单位 | Institute of Molecular Virology and Immunology,Department of Microbiology and Immunology,School of Basic Medical Sciences,Wenzhou Medical University,Wenzhou,325035,China |
第一作者单位 | 基础医学院(机能实验教学中心)_病原生物学与免疫学系 |
通讯作者单位 | 基础医学院(机能实验教学中心)_病原生物学与免疫学系 |
第一作者的第一单位 | 基础医学院(机能实验教学中心)_病原生物学与免疫学系 |
推荐引用方式 GB/T 7714 | Kamara, Saidu,Guo, Yanru,Mao, Shanshan,et al. Novel EBV LMP1 C-terminal domain binding affibody molecules as potential agents for in vivo molecular imaging diagnosis of nasopharyngeal carcinoma[J]. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY,2021,105(19):7283-7293. |
APA | Kamara, Saidu., Guo, Yanru., Mao, Shanshan., Ye, Xiaoxian., Li, Qingfeng., ... & Zhang, Lifang. (2021). Novel EBV LMP1 C-terminal domain binding affibody molecules as potential agents for in vivo molecular imaging diagnosis of nasopharyngeal carcinoma. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 105(19), 7283-7293. |
MLA | Kamara, Saidu,et al."Novel EBV LMP1 C-terminal domain binding affibody molecules as potential agents for in vivo molecular imaging diagnosis of nasopharyngeal carcinoma".APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 105.19(2021):7283-7293. |
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