H
Henry Tien
Researcher at Scripps Research Institute
Publications - 9
Citations - 951
Henry Tien is an academic researcher from Scripps Research Institute. The author has contributed to research in topics: Antibody & Epitope. The author has an hindex of 6, co-authored 7 publications receiving 672 citations. Previous affiliations of Henry Tien include University of California, San Diego.
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Journal ArticleDOI
Structural basis of a shared antibody response to SARS-CoV-2.
Meng Yuan,Hejun Liu,Nicholas C. Wu,Chang-Chun D Lee,Xueyong Zhu,Fangzhu Zhao,Deli Huang,Wenli Yu,Yuanzi Hua,Henry Tien,Thomas F. Rogers,Thomas F. Rogers,Elise Landais,Elise Landais,Devin Sok,Devin Sok,Joseph G. Jardine,Joseph G. Jardine,Dennis R. Burton,Ian A. Wilson +19 more
TL;DR: It is found that immunoglobulin G heavy-chain variable region 3-53 (IGHV3-53) is the most frequently used IGHV gene for targeting the receptor-binding domain (RBD) of the spike protein, which is promising for vaccine design.
Journal ArticleDOI
Supersite of immune vulnerability on the glycosylated face of HIV-1 envelope glycoprotein gp120
Leopold Kong,Jeong Hyun Lee,Katie J. Doores,Katie J. Doores,Katie J. Doores,Charles D. Murin,Jean-Philippe Julien,Jean-Philippe Julien,Ryan McBride,Yan Liu,Andre J. Marozsan,Albert Cupo,Per Johan Klasse,Simon Hoffenberg,Michael J. Caulfield,C. Richter King,Yuanzi Hua,Yuanzi Hua,Khoa Le,Khoa Le,Reza Khayat,Marc C. Deller,Thomas Clayton,Henry Tien,Ten Feizi,Rogier W. Sanders,Rogier W. Sanders,James C. Paulson,John P. Moore,Robyn L. Stanfield,Robyn L. Stanfield,Dennis R. Burton,Andrew B. Ward,Andrew B. Ward,Ian A. Wilson +34 more
TL;DR: Combined structural studies of PGT 135, PGT 128 and 2G12 show that this Asn332-dependent antigenic region is highly accessible and much more extensive than initially appreciated, which allows for multiple binding modes and varied angles of approach; thereby it represents a supersite of vulnerability for antibody neutralization.
Journal ArticleDOI
Crystal structure of the Fic (Filamentation induced by cAMP) family protein SO4266 (gi|24375750) from Shewanella oneidensis MR-1 at 1.6 A resolution.
Debanu Das,Sanjay Krishna,Sanjay Krishna,Daniel McMullan,Mitchell D. Miller,Qingping Xu,Polat Abdubek,Claire Acosta,Tamara Astakhova,Herbert L. Axelrod,Prasad Burra,Dennis Carlton,Hsiu-Ju Chiu,Thomas Clayton,Marc C. Deller,Lian Duan,Ylva Elias,Marc-André Elsliger,Dustin C. Ernst,Julie Feuerhelm,Anna Grzechnik,Slawomir K. Grzechnik,Joanna Hale,Gye Won Han,Lukasz Jaroszewski,Lukasz Jaroszewski,Kevin K. Jin,Heath E. Klock,Mark W. Knuth,Piotr Kozbial,Abhinav Kumar,David Marciano,Andrew T. Morse,Kevin D. Murphy,Edward Nigoghossian,Linda Okach,Silvya Oommachen,Jessica Paulsen,Ron Reyes,Christopher L. Rife,Natasha Sefcovic,Henry Tien,Christine B Trame,Christina V. Trout,Henry van den Bedem,Dana Weekes,Aprilfawn White,Keith O. Hodgson,John Wooley,Ashley M. Deacon,Adam Godzik,Adam Godzik,Scott A. Lesley,Scott A. Lesley,Ian A. Wilson +54 more
TL;DR: The protein SO4266 (Uniprot entry Q8E9K5_SHEON), at 372 amino acids, is one of the largest Fic domain-containing proteins to have its structure determined and together with the structures of the other Fic proteins paves the way for further structure-based functional characterization.
Journal ArticleDOI
A broad and potent neutralization epitope in SARS-related coronaviruses
Meng Yuan,Xu-Dong Zhu,Wan-ting He,Panpan Zhou,Chengzi I. Kaku,Tazio Capozzola,Connie Y. Zhu,Xinye Yu,Hejun Liu,Wenli Yu,Yuanzi Hua,Henry Tien,Linghang Peng,Ge Song,Christopher A. Cottrell,William R. Schief,David Nemazee,Laura M. Walker,Raiees Andrabi,Dennis R. Burton,Ian A. Wilson +20 more
TL;DR:
Posted ContentDOI
Structural basis of a public antibody response to SARS-CoV-2
Meng Yuan,Hejun Liu,Nicholas C. Wu,Chang-Chun D Lee,Xueyong Zhu,Fangzhu Zhao,Deli Huang,Wenli Yu,Yuanzi Hua,Henry Tien,Thomas F. Rogers,Thomas F. Rogers,Elise Landais,Elise Landais,Devin Sok,Devin Sok,Joseph G. Jardine,Joseph G. Jardine,Dennis R. Burton,Ian A. Wilson +19 more
TL;DR: IGHV3-53 represents a versatile public VH in neutralizing SARS-CoV-2 antibodies, where their specific germline features and minimal affinity maturation provide important insights for vaccine design and assessing outcomes.