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Molecular features of IGHV3-53-encoded antibodies elicited by SARS-CoV-2

机译:SARS-COV-2引发的IGHV3-53编码抗体的分子特征

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An elegant paper by Yuan et al., recently published in Science,provides novel insights into the molecular features of neutralizingantibody responses to the severe acute respiratory syndromecoronavirus 2 (SARS-CoV-2).1According to the principles of the “reverse vaccinology 2.0”postulated by Burton et al.,2 the authors explore the interactionsbetween potent neutralizing antibodies from naturally infecteddonors and their target epitopes, providing key information aboutstructural motifs and binding mode that may facilitate the designof vaccine antigens capable to elicit the immune response againstSARS-CoV-2. The vast majority of anti-CoV neutralizing antibodieshave been found to specifically target the receptor-bindingdomain (RBD) of the viral spike (S) protein, thus hindering SARSCoV-2binding to the host angiotensin converting enzyme 2(ACE2) receptor and viral entry.
机译:Yuan等人的优雅纸张,最近发表于科学,为对严重急性呼吸综合征反应的中和呼吸综合征的分子特征提供了新的洞察力对严重的急性呼吸道综合征反应的分子特征(SARS-COV-2)。1根据“反向疫苗学2.0”的原则.1由Burton等人假设,2作者探讨了来自天然感染的毒剂及其靶表表位的效力中和抗体的相互作用,提供了关于结构基序和结合模式的关键信息,其可以促进疫苗抗原的设计能够引发免疫应答的抗药性反应 - COV-2 。发现绝大多数的抗COV中和抗体汉族发现特异性地靶向病毒穗蛋白的受体结合族(RBD),从而阻碍SARSCOV-2BINDING到宿主血管紧张素转化酶2(ACE2)受体和病毒进入。

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