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6F6O

Structure of Adenovirus 3 fiber head V239D mutant

6F6O の概要
エントリーDOI10.2210/pdb6f6o/pdb
関連するPDBエントリー4wyj
分子名称Fiber protein (2 entities in total)
機能のキーワードadenovirus 3 fiber head, capsid protein, cell adhesion, viral protein
由来する生物種Human adenovirus B serotype 3 (HAdV-3)
タンパク質・核酸の鎖数1
化学式量合計21784.54
構造登録者
Zubieta, C.,Fender, P.,Stermann, E.,Lieber, A. (登録日: 2017-12-05, 公開日: 2018-12-19, 最終更新日: 2024-01-17)
主引用文献Richter, M.,Yumul, R.,Wang, H.,Saydaminova, K.,Ho, M.,May, D.,Baldessari, A.,Gough, M.,Drescher, C.,Urban, N.,Roffler, S.,Zubieta, C.,Carter, D.,Fender, P.,Lieber, A.
Preclinical safety and efficacy studies with an affinity-enhanced epithelial junction opener and PEGylated liposomal doxorubicin.
Mol Ther Methods Clin Dev, 2:15005-15005, 2015
Cited by
PubMed Abstract: A central treatment resistance mechanism in solid tumors is the maintenance of epithelial junctions between malignant cells that prevent drug penetration into the tumor. We have developed a small recombinant protein (JO-1) that triggers the transient opening of intercellular junctions and thus increases the efficacy of monoclonal antibodies and chemotherapeutic drugs without causing toxicity in mouse tumor models. Here, we provide data toward the clinical translation of an affinity-enhanced version of JO-1, which we call JO-4, in combination with PEGylated liposomal doxorubicin (PLD)/Doxil for ovarian cancer therapy. We have presented X-ray crystallography data suggesting a structural basis for the higher affinity of JO-4 to DSG2. We also confirmed JO-4 efficacy in a xenograft model with primary ovarian cancer cells showing that JO-4 can salvage Doxil therapy when given at a dose that was threefold lower than the therapeutic dose. Furthermore, we tested the safety of intravenous JO-4 alone and in combination with Doxil in Macaca fascicularis, an adequate animal model for predicting toxicity in humans. Our studies did not show critical JO-4-related toxicity or an increase of Doxil-related side effects. Our efficacy and safety data will help to support an Investigational new drug-filing for a JO-4/Doxil combination treatment.
PubMed: 26029716
DOI: 10.1038/mtm.2015.5
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.49 Å)
構造検証レポート
Validation report summary of 6f6o
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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