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Cited by 449

The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.

An ultrapotent synthetic nanobody neutralizes SARS-CoV-2 by stabilizing inactive Spike

Open access
Schoof, Michael, Faust, Bryan, Saunders, Reuben A., Sangwan, Smriti, Rezelj, Veronica, Hoppe, Nick, Boone, Morgane, Billesbølle, Christian B., Puchades, Cristina, Azumaya, Caleigh M., Kratochvil, Huong T., Zimanyi, Marcell, Deshpande, Ishan, Liang, Jiahao, Dickinson, Sasha, Nguyen, Henry C., Chio, Cynthia M., Merz, Gregory E., Thompson, Michael C., Diwanji, Devan, Schaefer, Kaitlin, Anand, Aditya A., Dobzinski, Niv, Zha, Beth Shoshana, Simoneau, Camille R., Leon, Kristoffer, White, Kris M., Chio, Un Seng, Gupta, Meghna, Jin, Mingliang, Li, Fei, Liu, Yanxin, Zhang, Kaihua, Bulkley, David, Sun, Ming, Smith, Amber M., Rizo, Alexandrea N., Moss, Frank, Brilot, Axel F., Pourmal, Sergei, Trenker, Raphael, Pospiech, Thomas, Gupta, Sayan, Barsi-Rhyne, Benjamin, Belyy, Vladislav, Barile-Hill, Andrew W., Nock, Silke, Liu, Yuwei, Krogan, Nevan J., Ralston, Corie Y., Swaney, Danielle L., García-Sastre, Adolfo, Ott, Melanie, Vignuzzi, Marco, QCRG Structural Biology Consortium, Walter, Peter, Manglik, Aashish, Azumaya, Caleigh M., Puchades, Cristina, Sun, Ming, Braxton, Julian R., Brilot, Axel F., Gupta, Meghna, Li, Fei, Lopez, Kyle E., Melo, Arthur, Merz, Gregory E., Moss, Frank, Paulino, Joana, Pospiech, Thomas H., Pourmal, Sergei, Rizo, Alexandrea N., Smith, Amber M., Thomas, Paul V., Wang, Feng, Yu, Zanlin, Dickinson, Miles Sasha, Nguyen, Henry C., Asarnow, Daniel, Campbell, Melody G., Chio, Cynthia M., Chio, Un Seng, Diwanji, Devan, Faust, Bryan, Gupta, Meghna, Hoppe, Nick, Jin, Mingliang, Li, Junrui, Liu, Yanxin, Merz, Gregory E., Sangwan, Smriti, Tsui, Tsz Kin Martin, Trenker, Raphael, Trinidad, Donovan, Tse, Eric, Zhang, Kaihua, Zhou, Fengbo, Herrera, Nadia, Kratochvil, Huong T., Schulze-Gahmen, Ursula, Thompson, Michael C., Young, Iris D., Biel, Justin, Deshpande, Ishan, Liu, Xi, Billesbølle, Christian Bache, Nowotny, Carlos, Smith, Amber M., Zhao, Jianhua, Bowen, Alisa, Hoppe, Nick, Li, Yen-Li, Nguyen, Phuong, Safari, Mali, Schaefer, Kaitlin, Whitis, Natalie, Moritz, Michelle, Owens, Tristan W., Diallo, Amy, Kim, Kate, Peters, Jessica K., Titus, Erron W., Chen, Jenny, Doan, Loan, Flores, Sebastian, Lam, Victor L., Li, Yang, Lo, Megan, Thwin, Aye C., Wankowicz, Stephanie, Zhang, Yang, Bulkley, David, Joves, Arceli, Joves, Almarie, McKay, Liam, Tabios, Mariano, Rosenberg, Oren S., Verba, Kliment A., Agard, David A., Cheng, Yifan, Fraser, James S., Frost, Adam, Jura, Natalia, Kortemme, Tanja, Krogan, Nevan J., Manglik, Aashish, Southworth, Daniel R., Stroud, Robert M.·2020·Science

Abstract

Nanobodies that neutralize: Monoclonal antibodies that bind to the spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) show therapeutic promise but must be produced in mammalian cells and need to be delivered intravenously. By contrast, single-domain antibodies called nanobodies can be produced in bacteria or yeast, and their stability may enable aerosol delivery. Two papers now report nanobodies that bind tightly to spike and efficiently neutralize SARS-CoV-2 in cells. Schoof et al. screened a yeast surface display of synthetic nanobodies and Xiang et al. screened anti-spike nanobodies produced by a llama. Both groups identified highly potent nanobodies that lock the spike protein in an inactive conformation. Multivalent constructs of selected nanobodies achieved even more potent neutralization. Science , this issue p. 1473 , p. 1479

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Metadata

Authors
Schoof, M., Faust, B., Saunders, R. A., Sangwan, S., Rezelj, V., Hoppe, N., Boone, M., Billesbølle, C. B., Puchades, C., Azumaya, C. M., Kratochvil, H. T., Zimanyi, M., Deshpande, I., Liang, J., Dickinson, S., Nguyen, H. C., Chio, C. M., Merz, G. E., Thompson, M. C., Diwanji, D., Schaefer, K., Anand, A. A., Dobzinski, N., Zha, B. S., Simoneau, C. R., Leon, K., White, K. M., Chio, U. S., Gupta, M., Jin, M., Li, F., Liu, Y., Zhang, K., Bulkley, D., Sun, M., Smith, A. M., Rizo, A. N., Moss, F., Brilot, A. F., Pourmal, S., Trenker, R., Pospiech, T., Gupta, S., Barsi-Rhyne, B., Belyy, V., Barile-Hill, A. W., Nock, S., Liu, Y., Krogan, N. J., Ralston, C. Y., Swaney, D. L., García-Sastre, A., Ott, M., Vignuzzi, M., QCRG Structural Biology Consortium, Walter, P., Manglik, A., Azumaya, C. M., Puchades, C., Sun, M., Braxton, J. R., Brilot, A. F., Gupta, M., Li, F., Lopez, K. E., Melo, A., Merz, G. E., Moss, F., Paulino, J., Pospiech, T. H., Pourmal, S., Rizo, A. N., Smith, A. M., Thomas, P. V., Wang, F., Yu, Z., Dickinson, M. S., Nguyen, H. C., Asarnow, D., Campbell, M. G., Chio, C. M., Chio, U. S., Diwanji, D., Faust, B., Gupta, M., Hoppe, N., Jin, M., Li, J., Liu, Y., Merz, G. E., Sangwan, S., Tsui, T. K. M., Trenker, R., Trinidad, D., Tse, E., Zhang, K., Zhou, F., Herrera, N., Kratochvil, H. T., Schulze-Gahmen, U., Thompson, M. C., Young, I. D., Biel, J., Deshpande, I., Liu, X., Billesbølle, C. B., Nowotny, C., Smith, A. M., Zhao, J., Bowen, A., Hoppe, N., Li, Y.-L., Nguyen, P., Safari, M., Schaefer, K., Whitis, N., Moritz, M., Owens, T. W., Diallo, A., Kim, K., Peters, J. K., Titus, E. W., Chen, J., Doan, L., Flores, S., Lam, V. L., Li, Y., Lo, M., Thwin, A. C., Wankowicz, S., Zhang, Y., Bulkley, D., Joves, A., Joves, A., McKay, L., Tabios, M., Rosenberg, O. S., Verba, K. A., Agard, D. A., Cheng, Y., Fraser, J. S., Frost, A., Jura, N., Kortemme, T., Krogan, N. J., Manglik, A., Southworth, D. R., & Stroud, R. M.
Venue
Science
Published
2020-12-18
Volume
370
Issue
6523
Pages
1473-1479
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W3096751000
Cited by
449
References
22
FWCI
10.89
Type
journal article
Language
en
Open access
hybrid

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Schoof, M., Faust, B., Saunders, R. A., Sangwan, S., Rezelj, V., Hoppe, N., Boone, M., Billesbølle, C. B., Puchades, C., Azumaya, C. M., Kratochvil, H. T., Zimanyi, M., Deshpande, I., Liang, J., Dickinson, S., Nguyen, H. C., Chio, C. M., Merz, G. E., Thompson, M. C., . . . Stroud, R. M. (2020). An ultrapotent synthetic nanobody neutralizes SARS-CoV-2 by stabilizing inactive Spike. Science. https://doi.org/10.1126/science.abe3255

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