<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Huang J</submitter><funding>Coalition for Epidemic Preparedness Innovations (CEPI)</funding><funding>Coalition for Epidemic Preparedness Innovations</funding><pagination>1455-1464</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9878482</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>415(8)</volume><pubmed_abstract>COVID-19 is caused by SARS-CoV-2 infection and remains one of the biggest pandemics around the world since 2019. Vaccination has proved to be an effective way of preventing SARS-CoV-2 infection and alleviating the hospitalization burden. Among different forms of COVID-19 vaccine design, the spike protein of SARS-CoV-2 virus is widely used as a candidate vaccine antigen. As a surface protein on the virus envelop, the spike was reported to be heavily N-glycosylated and glycosylation had a great impact on its immunogenicity and efficacy. Besides, N-glycosylation might vary greatly on different expression systems and sequence variant designs. Therefore, comprehensive analysis of spike N-glycosylation is of great significance for better vaccine understanding and quality control. In this study, </pubmed_abstract><journal>Analytical and bioanalytical chemistry</journal><pubmed_title>In-depth characterization of protein N-glycosylation for a COVID-19 variant-design vaccine spike protein.</pubmed_title><pmcid>PMC9878482</pmcid><funding_grant_id>RRZE2101</funding_grant_id><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Zhou C</pubmed_authors><pubmed_authors>An J</pubmed_authors><pubmed_authors>Hou S</pubmed_authors></additional><is_claimable>false</is_claimable><name>In-depth characterization of protein N-glycosylation for a COVID-19 variant-design vaccine spike protein.</name><description>COVID-19 is caused by SARS-CoV-2 infection and remains one of the biggest pandemics around the world since 2019. Vaccination has proved to be an effective way of preventing SARS-CoV-2 infection and alleviating the hospitalization burden. Among different forms of COVID-19 vaccine design, the spike protein of SARS-CoV-2 virus is widely used as a candidate vaccine antigen. As a surface protein on the virus envelop, the spike was reported to be heavily N-glycosylated and glycosylation had a great impact on its immunogenicity and efficacy. Besides, N-glycosylation might vary greatly on different expression systems and sequence variant designs. Therefore, comprehensive analysis of spike N-glycosylation is of great significance for better vaccine understanding and quality control. In this study, </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-05-28T03:48:11.626Z</modification><creation>2024-12-03T21:40:31.079Z</creation></dates><accession>S-EPMC9878482</accession><cross_references><pubmed>36698045</pubmed><doi>10.1007/s00216-023-04533-w</doi></cross_references></HashMap>