HIV-1 neutralizing antibodies in SHIV-infected macaques recapitulate structurally divergent modes of human V2 apex recognition with a single D gene.
Ryan S RoarkRumi HabibJason GormanHui LiAndrew Jesse ConnellMattia BonsignoriYicheng GuoMichael P HogartyAdam S OliaKirsten SowersBaoshan ZhangFrederic Bibollet-RucheSean CallaghanJohn W CareyGabriele CeruttiDarcy R HarrisWanting HeEmily LewisTracy LiuRosemarie D MasonYounghoon ParkJuliette M RandoAjay SinghJeremy WolffQ Paula LeiMark K LouderNicole A Doria-RoseRaiees AndrabiKevin O SaundersMichael S SeamanBarton F HaynesDaniel W KulpJohn R MascolaMario RoedererZizhang ShengBeatrice H HahnGeorge M ShawPeter D KwongLawrence ShapiroPublished in: bioRxiv : the preprint server for biology (2024)
Isolated 11 V2 apex-targeted HIV-neutralizing lineages from 10 SHIV-infected Indian-origin rhesus macaquesCryo-EM structures of Fab-Env complexes for nine rhesus lineages reveal modes of recognition that mimic three modes of human V2 apex antibody recognitionAll SHIV-elicited V2 apex lineages, including two others previously published, derive from the same DH3-15*01 gene utilizing reading frame twoThe DH3-15*01 gene in reading frame two provides a necessary, but not sufficient, signature for V2 apex-directed broadly neutralizing antibodiesStructural roles played by DH3-15*01-encoded amino acids differed substantially in different lineages, even for those with the same recognition modePropose that the anionic, aromatic, and extended character of DH3-15*01 in reading frame two provides a selective advantage for V2 apex recognition compared to B cells derived from other D genes in the naïve rhesus repertoireDemonstrate that highly selected genetic elements can play multiple roles in antigen recognition, providing a structural means to enhance recognition diversity.
Keyphrases
- genome wide
- copy number
- endothelial cells
- antiretroviral therapy
- hiv infected
- genome wide identification
- working memory
- hepatitis c virus
- amino acid
- human immunodeficiency virus
- hiv positive
- dna methylation
- hiv aids
- dengue virus
- systematic review
- induced pluripotent stem cells
- genome wide analysis
- mass spectrometry
- men who have sex with men
- cancer therapy
- single cell
- drug delivery