3S1B
The Development of Peptide-based Tools for the Analysis of Angiogenesis
3S1B の概要
エントリーDOI | 10.2210/pdb3s1b/pdb |
関連するPDBエントリー | 3S1K |
分子名称 | Vascular endothelial growth factor A, mini-Z (2 entities in total) |
機能のキーワード | vegf, cystine knot, mini-z, signaling protein |
由来する生物種 | Homo sapiens (human) 詳細 |
細胞内の位置 | Secreted: P15692 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 15257.57 |
構造登録者 | |
主引用文献 | Fedorova, A.,Zobel, K.,Gill, H.S.,Ogasawara, A.,Flores, J.E.,Tinianow, J.N.,Vanderbilt, A.N.,Wu, P.,Meng, Y.G.,Williams, S.P.,Wiesmann, C.,Murray, J.,Marik, J.,Deshayes, K. The development of Peptide-based tools for the analysis of angiogenesis. Chem.Biol., 18:839-845, 2011 Cited by PubMed Abstract: Limitations to the application of molecularly targeted cancer therapies are the inability to accurately match patient with effective treatment and the absence of a prompt readout of posttreatment response. Noninvasive agents that rapidly report vascular endothelial growth factor (VEGF) levels using positron emission tomography (PET) have the potential to enhance anti-angiogenesis therapies. Using phage display, two distinct classes of peptides were identified that bind to VEGF with nanomolar affinity and high selectivity. Co-crystal structures of these different peptide classes demonstrate that both bind to the receptor-binding region of VEGF. (18)F-radiolabelling of these peptides facilitated the acquisition of PET images of tumor VEGF levels in a HM7 xenograph model. The images obtained from one 59-residue probe, (18)F-Z-3B, 2 hr postinjection are comparable to those obtained with anti-VEGF antibody B20 72 hr postinjection. Furthermore, VEGF levels in growing SKOV3 tumors were followed using (18)F-Z-3B as a PET probe with VEGF levels increasing with tumor size. PubMed: 21802005DOI: 10.1016/j.chembiol.2011.05.011 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.9 Å) |
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