7T62
GPC2 HEP CT3 complex
7T62 の概要
エントリーDOI | 10.2210/pdb7t62/pdb |
EMDBエントリー | 25708 |
分子名称 | Glypican-2, CT3 (2 entities in total) |
機能のキーワード | glypican-3 complex, immune system |
由来する生物種 | Homo sapiens (human) 詳細 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 108361.62 |
構造登録者 | Zhu, J.,Cachau, R.,De Val Alda, N.,Li, N.,Ho, M. (登録日: 2021-12-13, 公開日: 2021-12-22, 最終更新日: 2024-10-23) |
主引用文献 | Li, N.,Torres, M.B.,Spetz, M.R.,Wang, R.,Peng, L.,Tian, M.,Dower, C.M.,Nguyen, R.,Sun, M.,Tai, C.H.,de Val, N.,Cachau, R.,Wu, X.,Hewitt, S.M.,Kaplan, R.N.,Khan, J.,St Croix, B.,Thiele, C.J.,Ho, M. CAR T cells targeting tumor-associated exons of glypican 2 regress neuroblastoma in mice. Cell Rep Med, 2:100297-100297, 2021 Cited by PubMed Abstract: Targeting solid tumors must overcome several major obstacles, in particular, the identification of elusive tumor-specific antigens. Here, we devise a strategy to help identify tumor-specific epitopes. Glypican 2 (GPC2) is overexpressed in neuroblastoma. Using RNA sequencing (RNA-seq) analysis, we show that exon 3 and exons 7-10 of GPC2 are expressed in cancer but are minimally expressed in normal tissues. Accordingly, we discover a monoclonal antibody (CT3) that binds exons 3 and 10 and visualize the complex structure of CT3 and GPC2 by electron microscopy. The potential of this approach is exemplified by designing CT3-derived chimeric antigen receptor (CAR) T cells that regress neuroblastoma in mice. Genomic sequencing of T cells recovered from mice reveals the CAR integration sites that may contribute to CAR T cell proliferation and persistence. These studies demonstrate how RNA-seq data can be exploited to help identify tumor-associated exons that can be targeted by CAR T cell therapies. PubMed: 34195677DOI: 10.1016/j.xcrm.2021.100297 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (21 Å) |
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