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5U64

Camel nanobody VHH-28

5U64 の概要
エントリーDOI10.2210/pdb5u64/pdb
関連するPDBエントリー5U65
分子名称VHH-28 (2 entities in total)
機能のキーワードneutralizing antibody, camel vhh nanobody, hiv-1, immune system
由来する生物種Camelus dromedarius
タンパク質・核酸の鎖数1
化学式量合計15020.44
構造登録者
Stanfield, R.L.,Wilson, I.A. (登録日: 2016-12-07, 公開日: 2017-09-20, 最終更新日: 2024-10-30)
主引用文献Koch, K.,Kalusche, S.,Torres, J.L.,Stanfield, R.L.,Danquah, W.,Khazanehdari, K.,von Briesen, H.,Geertsma, E.R.,Wilson, I.A.,Wernery, U.,Koch-Nolte, F.,Ward, A.B.,Dietrich, U.
Selection of nanobodies with broad neutralizing potential against primary HIV-1 strains using soluble subtype C gp140 envelope trimers.
Sci Rep, 7:8390-8390, 2017
Cited by
PubMed Abstract: Broadly neutralizing antibodies (bnAbs) against HIV-1 protect from infection and reduce viral load upon therapeutic applications. However no vaccine was able so far to induce bnAbs demanding their expensive biotechnological production. For clinical applications, nanobodies (VHH) derived from heavy chain only antibodies from Camelidae, may be better suited due to their small size, high solubility/stability and extensive homology to human VH3 genes. Here we selected broadly neutralizing nanobodies by phage display after immunization of dromedaries with different soluble trimeric envelope proteins derived from HIV-1 subtype C. We identified 25 distinct VHH families binding trimeric Env, of which 6 neutralized heterologous primary isolates of various HIV-1 subtypes in a standardized in vitro neutralization assay. The complementary neutralization pattern of two selected VHHs in combination covers 19 out of 21 HIV-1 strains from a standardized panel of epidemiologically relevant HIV-1 subtypes. The CD4 binding site was preferentially targeted by the broadly neutralizing VHHs as determined by competition ELISAs and 3D models of VHH-Env complexes derived from negative stain electron microscopy. The nanobodies identified here are excellent candidates for further preclinical/clinical development for prophylactic and therapeutic applications due to their potency and their complementary neutralization patterns covering the majority of epidemiologically relevant HIV-1 subtypes.
PubMed: 28827559
DOI: 10.1038/s41598-017-08273-7
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.153 Å)
構造検証レポート
Validation report summary of 5u64
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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