Online education has long been suffering from high dropout rate and low achievement. However, both asynchronous and synchronous online instructions have to become effective to serve as a quick response to maintain undisrupted learning during the COVID-19 outbreak. The purpose of the present study was to examine student engagement, learning outcome, and students' perceptions of an online course featured with frequent tasks, quizzes, and tests as formative assessment. Data were collected from the first five weeks of a course that was temporarily converted from blended learning to be fully online in time of school closure. Analysis of students' learning records and scores indicated that students engaged themselves actively in all of the online learning activities and had gained high scores in all tasks, quizzes, and tests. In addition, students held positive perceptions towards the formative assessment.
The spike (S) protein plays a key role in COVID-19 (SARS-CoV-2)
infection and host-cell entry. Previous studies have systematically
analyzed site-specific glycan compositions as well as many important
structural motifs of the S protein. Here, we further provide structural-clear
N-
glycosylation of the S protein at a site-specific level
by using our recently developed structural- and site-specific
N-
glycoproteomics sequencing algorithm, StrucGP. In addition
to the common
N-
glycans as detected in previous studies,
many uncommon glycosylation structures such as LacdiNAc structures,
Lewis structures, Mannose 6-phosphate (M6P) residues, and bisected
core structures were unambiguously mapped at a total of 20 glycosites
in the S protein trimer and protomer. These data further support the
glycosylation structural–functional investigations of the COVID-19
virus spike.
N-Linked glycoproteins are rich in seminal plasma, playing various essential roles in supporting sperm function and the fertilization process. However, the detailed information on these glycoproteins, particularly site-specific glycan structures, is still limited. In this study, a precision site-specific N-glycoproteome map of human seminal plasma was established by employing the site-specific glycoproteomic approach and a recently developed glycan structure interpretation software, StrucGP. A total of 9567 unique glycopeptides identified in human seminal plasma were composed of 773 N-linked glycan structures and 1019 N-glycosites from 620 glycoproteins. These glycans were comprised of four types of core structures and 13 branch structures. The majority of identified glycoproteins functioned in response to stimulus and immunity. As we reported in human spermatozoa, heavy fucosylation (fucose residues ≥6 per glycan) was also detected on seminal plasma glycoproteins such as clusterin and galectin-3-binding protein, which were involved in the immune response of biological processes and reactome pathways. Comparison of site-specific glycans between seminal plasma and spermatozoa revealed more complicated glycan structures in seminal plasma than in spermatozoa, even on their shared glycoproteins. These present data will be greatly beneficial for the in-depth structural and functional study of glycosylation in the male reproduction system.
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