7SG5
Structure of PfCSP peptide 21 with antibody CIS43_Var2
7SG5 の概要
エントリーDOI | 10.2210/pdb7sg5/pdb |
分子名称 | CIS43_Var2 Fab Heavy chain, CIS43_Var2 Fab Light chain, PfCSP peptide 21, ... (6 entities in total) |
機能のキーワード | antibody, plasmodium falciparum, immune system |
由来する生物種 | Homo sapiens (human) 詳細 |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 50589.01 |
構造登録者 | |
主引用文献 | Banach, B.B.,Tripathi, P.,Da Silva Pereira, L.,Gorman, J.,Nguyen, T.D.,Dillon, M.,Fahad, A.S.,Kiyuka, P.K.,Madan, B.,Wolfe, J.R.,Bonilla, B.,Flynn, B.,Francica, J.R.,Hurlburt, N.K.,Kisalu, N.K.,Liu, T.,Ou, L.,Rawi, R.,Schon, A.,Shen, C.H.,Teng, I.T.,Zhang, B.,Pancera, M.,Idris, A.H.,Seder, R.A.,Kwong, P.D.,DeKosky, B.J. Highly protective antimalarial antibodies via precision library generation and yeast display screening. J.Exp.Med., 219:-, 2022 Cited by PubMed Abstract: The monoclonal antibody CIS43 targets the Plasmodium falciparum circumsporozoite protein (PfCSP) and prevents malaria infection in humans for up to 9 mo following a single intravenous administration. To enhance the potency and clinical utility of CIS43, we used iterative site-saturation mutagenesis and DNA shuffling to screen precise gene-variant yeast display libraries for improved PfCSP antigen recognition. We identified several mutations that improved recognition, predominately in framework regions, and combined these to produce a panel of antibody variants. The most improved antibody, CIS43_Var10, had three mutations and showed approximately sixfold enhanced protective potency in vivo compared to CIS43. Co-crystal and cryo-electron microscopy structures of CIS43_Var10 with the peptide epitope or with PfCSP, respectively, revealed functional roles for each of these mutations. The unbiased site-directed mutagenesis and screening pipeline described here represent a powerful approach to enhance protective potency and to enable broader clinical use of antimalarial antibodies. PubMed: 35736810DOI: 10.1084/jem.20220323 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.4 Å) |
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