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Figure S1 D). Gene usage (gene), somatic hypermutation % (SHM) of heavy and light chains, and CDRH3 amino acids (aa) and length were analyzed by IMGT vquest. Data shown in (A) and (B) are represented as means ± SD (n = 3). See also Journal: Cell Reports
Article Title: Resistance of SARS-CoV-2 variants to neutralization by antibodies induced in convalescent patients with COVID-19
doi: 10.1016/j.celrep.2021.109385
Figure Lengend Snippet: Characterization of five neutralizing mAbs (A) Neutralization of SARS-CoV-2 pseudovirus by mAbs 6-74, 3-5, 8-92, 10-121, and 9-105 in 293FT/ACE2/TMPRSS2, Calu-3 (human lung cancer cell line), and Caco-2 (human colon adenocarcinoma cell line) cells is shown. A non-neutralizing mAb, 8-38, was used as a negative control (orange open circle). (B) Cell fusion of 293FT/DSP8-11/SARS-CoV-2-S cells with 293FT/DSP1-7/ACE2/TMPRSS2 and Calu-3/DSP1-7 cells was measured by luciferase activity at 6 and 20 h after coculture, respectively. A non-neutralizing mAb, 5-76, was used as a negative control (orange open circle). (C) IC 50 values of the five mAbs are summarized. (D) The binding and genetic characteristics of mAbs are summarized. Binding to RBD and NTD was analyzed by AlphaScreen. K D values were determined by SPR analysis (
Article Snippet:
Techniques: Neutralization, Negative Control, Luciferase, Activity Assay, Binding Assay, Amplified Luminescent Proximity Homogenous Assay