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6T3O

Crystal structure of the human myomesin domain 10

6T3O の概要
エントリーDOI10.2210/pdb6t3o/pdb
分子名称Myomesin-1, AZIDE ION (3 entities in total)
機能のキーワードsmall protein domain, scaffold structure, contractile protein
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数1
化学式量合計15437.46
構造登録者
Duskova, J.,Petrokova, H.,Maly, P. (登録日: 2019-10-11, 公開日: 2021-03-17, 最終更新日: 2024-01-24)
主引用文献Kuchar, M.,Kosztyu, P.,Daniel Liskova, V.,Cerny, J.,Petrokova, H.,Vroblova, E.,Maly, M.,Vankova, L.,Krupka, M.,Raskova Kafkova, L.,Turanek Knotigova, P.,Duskova, J.,Dohnalek, J.,Masek, J.,Turanek, J.,Raska, M.,Maly, P.
Myomedin scaffold variants targeted to 10E8 HIV-1 broadly neutralizing antibody mimic gp41 epitope and elicit HIV-1 virus-neutralizing sera in mice.
Virulence, 12:1271-1287, 2021
Cited by
PubMed Abstract: One of the proposed strategies for the development of a more efficient HIV-1 vaccine is based on the identification of proteins binding to a paratope of chosen broadly neutralizing antibody (bNAb) that will mimic cognate HIV-1 Env (glyco)protein epitope and could be used as potent immunogens for induction of protective virus-neutralizing antibodies in the immunized individuals. To verify this "non-cognate ligand" concept, we developed a highly complex combinatorial library designed on a scaffold of human myomesin-1 protein domain and selected proteins called Myomedins specifically binding to variable regions of HIV-1 broadly neutralizing antibody 10E8. Immunization of mice with these Myomedin variants elicited the production of HIV-1 Env-specific antibodies. Hyperimmune sera bound to Env pseudotyped viruses and weakly/moderately neutralized 54% of tested clade A, B, C, and AE pseudotyped viruses variants . These results demonstrate that Myomedin variants have the potential to mimic Env epitopes and could be used as potential HIV-1 vaccine components.
PubMed: 33993840
DOI: 10.1080/21505594.2021.1920251
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.8 Å)
構造検証レポート
Validation report summary of 6t3o
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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