Author
S. C. Harrison
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
Biology Disciplines
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2018-2023 · peak 3/yrCo-Author Collaboration Network
10 top collaborators · 16 mutual co-author links12 papers
Recent·Most cited
The rotavirus VP5*/VP8* conformational transition permeabilizes membranes to Ca2+
M. de Sautu, T. Herrmann, S. Jenni, S. C. Harrison
This study confirms that the rotavirus VP5*/VP8* conformational transition enables membrane permeabilization to Ca2+ through C-terminal segment insertion.
bioRxiv · Oct 15, 2023Microbiology
Structures of the Ndc80 complex and its interactions at the yeast kinetochore-microtubule interface
J. Zahm, S. Jenni, S. C. Harrison
The paper uses AlphaFold 2 to predict and validate the structure of the Ndc80 complex and its interactions with the Dam1 complex, revealing how phosphorylation regulates kinetochore-microtubule attachments.
bioRxiv · Nov 9, 2022Biochemistry
Infant antibody repertoires during the first two years of influenza vaccination
M. Kuraoka, N. C. Curtis, A. Watanabe, H. Tanno, S. Shin, K. Ye, E. Macdonald, O. Lavidor, S. Kong, T. Von Holle, I. W. Windsor, G. C. Ippolito, G. Georgiou, E. B. Walter, G. H. Kelsoe, , J. Lee
This paper studies how influenza vaccination in infants shapes their antibody responses, finding that vaccination can lead to immune imprinting similar to infection, with shifts in B-cell specificity and adult-like antibody repertoires after the second year.
bioRxiv · Sep 13, 2022Immunology
Recall of B cell memory depends on relative locations of prime and boost
M. Kuraoka, C.-H. Yeh, G. Bajic, R. Kotaki, S. Song, S. C. Harrison, G. Kelsoe
The study shows that memory B cells form recall germinal centers more effectively when boosts are given at the same site as the initial immunization, leading to higher mutation levels and avidity in BCRs.
bioRxiv · Dec 17, 2021 · PreprintImmunology
Recognition of Divergent Viral Substrates by the SARS-CoV-2 Main Protease
E. A. MacDonald, G. Frey, M. Namchuk, S. C. Harrison, S. M. Hinshaw, I. W. Windsor
This study presents crystal structures of SARS-CoV-2 Mpro bound to viral substrate peptides, revealing how peptide sequences influence catalytic efficiency and providing insights for antiviral drug design.
bioRxiv · Apr 20, 2021Biochemistry
Memory B cell repertoire for recognition of evolving SARS-CoV-2 spike
P. Tong, A. Gautam, I. Windsor, M. Travers, Y. Chen, N. Garcia, N. Whiteman, L. McKay, F. J. N. Lelis, S. Habibi, Y. Cai, L. J. Rennick, W. P. Duprex, K. McCarthy, C. L. Lavine, , D. R. Wesemann
The paper maps memory B cell receptors against SARS-CoV-2 spike variants, identifying 7 mAb competition groups and their epitopic regions, and shows their cross-reactivity and neutralization properties.
bioRxiv · Mar 10, 2021Immunology
The structural basis for Ulp2 recruitment to the kinetochore
Y. Quan, S. M. Hinshaw, P.-C. Wang, S. C. Harrison, H. Zhou
This study identifies a mechanism for regulated kinetochore sumoylation by showing that Ulp2 recruitment to Ctf3/CENP-I controls sumoylation levels and chromosome segregation.
bioRxiv · Dec 30, 2020Cell Biology
Structural Basis of Stu2 Recruitment to Yeast Kinetochores
J. A. Zahm, M. G. Stewart, J. S. Carrier, S. C. Harrison, M. P. Miller
This study identifies the structural basis of Stu2 recruitment to yeast kinetochores by showing its interaction with the Ndc80 complex, which is essential for tension-dependent stabilization of kinetochore-microtubule attachments.
bioRxiv · Oct 31, 2020Biochemistry
Structures of the ATP-fueled ClpXP proteolytic machine bound to protein substrate
X. Fei, T. A. Bell, S. Jenni, B. M. Stinson, T. A. Baker, S. C. Harrison, R. T. Sauer
This study presents cryo-EM structures of the E. coli ClpXP protease complex, revealing how ClpX interacts with ClpP and substrates, and proposes models for its ATP-dependent proteolytic mechanism.
bioRxiv · Oct 31, 2019Biophysics
How small-molecule inhibitors of dengue-virus infection interfere with viral membrane fusion
L. H. Chao, J. Jang, A. Johnson, A. Nguyen, N. S. Gray, P. L. Yang, S. C. Harrison
The paper studies how small-molecule inhibitors block dengue virus membrane fusion by targeting the envelope protein's conformational change, showing that ~15 bound molecules per particle prevent fusion.
bioRxiv · Jul 9, 2018Biophysics