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9MSD

G002-293-0536 Fab in complex with 001428_T278M_L14 SOSIP and RM20A3 Fab

これはPDB形式変換不可エントリーです。
9MSD の概要
エントリーDOI10.2210/pdb9msd/pdb
EMDBエントリー48575
分子名称001428_T278M_L14 SOSIP gp140, G002-293-0536 Fab heavy chain, G002-293-0536 Fab light chain, ... (8 entities in total)
機能のキーワードg002, clinical trial, hiv-1, vrc01, human antibody, vaccine, env, viral protein, viral protein-immune system complex, viral protein/immune system
由来する生物種Human immunodeficiency virus 1
詳細
タンパク質・核酸の鎖数15
化学式量合計509483.33
構造登録者
Phulera, S.,Ozorowski, G.,Ward, A.B. (登録日: 2025-01-09, 公開日: 2025-05-28)
主引用文献Willis, J.R.,Prabhakaran, M.,Muthui, M.,Naidoo, A.,Sincomb, T.,Wu, W.,Cottrell, C.A.,Landais, E.,deCamp, A.C.,Keshavarzi, N.R.,Kalyuzhniy, O.,Lee, J.H.,Murungi, L.M.,Ogonda, W.A.,Yates, N.L.,Corcoran, M.M.,Phulera, S.,Musando, J.,Tsai, A.,Lemire, G.,Sein, Y.,Muteti, M.,Alamuri, P.,Bohl, J.A.,Holman, D.,Himansu, S.,Leav, B.,Reuter, C.,Lin, L.A.,Ding, B.,He, C.,Straus, W.L.,MacPhee, K.J.,Regadas, I.,Nyabundi, D.V.,Chirchir, R.,Anzala, A.,Kimotho, J.N.,Kibet, C.,Greene, K.,Gao, H.,Beatman, E.,Benson, K.,Laddy, D.,Brown, D.M.,Bronson, R.,Baptiste, J.,Gajjala, S.,Rikhtegaran-Tehrani, Z.,Benner, A.,Ramaswami, M.,Lu, D.,Alavi, N.,Amirzehni, S.,Kubitz, M.,Tingle, R.,Georgeson, E.,Phelps, N.,Adachi, Y.,Liguori, A.,Flynn, C.,McKenney, K.,Zhou, X.,Owuor, D.C.,Owuor, S.,Kim, S.Y.,Duff, M.,Kim, J.Y.,Gibson, G.,Baboo, S.,Diedrich, J.,Schiffner, T.,Shields, M.,Matsoso, M.,Santos, J.,Syvertsen, K.,Kennedy, A.,Schroeter, M.,Vekemans, J.,Yates, J.,Paulson, J.C.,Hyrien, O.,McDermott, A.B.,Maenetje, P.,Nyombayire, J.,Karita, E.,Ingabire, R.,Edward, V.,Muturi-Kioi, V.,Maenza, J.,Shapiro, A.E.,McElrath, M.J.,Edupuganti, S.,Taylor, B.S.,Diemert, D.,Ozorowski, G.,Koup, R.A.,Montefiori, D.,Ward, A.B.,Hedestam, G.K.,Tomaras, G.,Hunt, D.J.,Muema, D.,Sok, D.,Laufer, D.S.,Andrews, S.F.,Nduati, E.W.,Schief, W.R.
Vaccination with mRNA-encoded nanoparticles drives early maturation of HIV bnAb precursors in humans.
Science, :eadr8382-eadr8382, 2025
Cited by
PubMed Abstract: A leading HIV vaccine strategy requires a priming immunogen to induce broadly neutralizing antibody (bnAb) precursors, followed by a series of heterologous boosters to elicit somatic hypermutation (SHM) and produce bnAbs. In two randomized, open-label phase 1 human clinical trials, IAVI-G002 in the United States and IAVI-G003 in Rwanda and South Africa, we evaluated the safety and immunogenicity of mRNA-encoded nanoparticles as priming immunogens (both trials) and first-boosting immunogens (IAVI-G002). The vaccines were generally safe and well tolerated, except 18% of IAVI-G002 participants experienced skin reactions. Priming induced bnAb precursors with substantial frequencies and SHM, and heterologous boosting elicited increased SHM, affinity, and neutralization activity toward bnAb development. The results establish clinical proof of concept that heterologous boosting can advance bnAb-precursor maturation and demonstrate bnAb priming in Africa where the HIV burden is highest.
PubMed: 40373112
DOI: 10.1126/science.adr8382
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.2 Å)
構造検証レポート
Validation report summary of 9msd
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2025-07-16に公開中

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