Evidence map›Paper›PMID 33684258›Full record

ArticleAngewandte Chemie (International ed. in English)2021

Neutralizing Aptamers Block S/RBD-ACE2 Interactions and Prevent Host Cell Infection.

Xiaohui Liu, Yi-Ling Wang, Jacky Wu, Jianjun Qi, Zihua Zeng, Quanyuan Wan, Zhenghu Chen, Pragya Manandhar, Victoria S Cavener, Nina R Boyle and 10 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

67 citing papers in PubMed.

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7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Xiaohui LiuDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.ORCID 0000-0002-4472-994X
Yi-Ling WangCenter for Immunotherapy Research, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Jacky WuDepartment of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signalling, University of Houston, Houston, TX, 77204, USA.
Jianjun QiDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Zihua ZengDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Quanyuan WanDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Zhenghu ChenDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Pragya ManandharDepartment of Biology and Biochemistry, University of Houston, Houston, TX, 77204, USA.
Victoria S CavenerAnimal Diagnostic Laboratory, Dept. of Veterinary and Biomedical Sciences, Huck Institutes of Life Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
Nina R BoyleAnimal Diagnostic Laboratory, Dept. of Veterinary and Biomedical Sciences, Huck Institutes of Life Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
Xinping FuDepartment of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signalling, University of Houston, Houston, TX, 77204, USA.
Eric SalazarDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Suresh V KuchipudiAnimal Diagnostic Laboratory, Dept. of Veterinary and Biomedical Sciences, Huck Institutes of Life Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
Vivek KapurDept. of Animal Science and Huck Institutes of Life Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
Xiaoliu ZhangDepartment of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signalling, University of Houston, Houston, TX, 77204, USA.
Michihisa UmetaniDepartment of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signalling, University of Houston, Houston, TX, 77204, USA.
Mehmet SenDepartment of Biology and Biochemistry, University of Houston, Houston, TX, 77204, USA.
Richard C WillsonChemical and Biomolecular Engineering, University of Houston, Houston, TX, 77204, USA.
Shu-Hsia ChenCenter for Immunotherapy Research, Houston Methodist Research Institute, Houston, TX, 77030, USA.
Youli ZuDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.ORCID 0000-0001-8574-9974

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 spike (S) protein plays a central role in mediating the first step of virus infection to cause disease: virus binding to angiotensin-converting enzyme 2 (ACE2) receptors on human host cells. Therefore, S/RBD is an ideal target for blocking and neutralization therapies to prevent and treat coronavirus disease 2019 (COVID-19). Using a target-based selection approach, we developed oligonucleotide aptamers containing a conserved sequence motif that specifically targets S/RBD. Synthetic aptamers had high binding affinity for S/RBD-coated virus mimics (K

Indexed as

COVID-19 Drug TreatmentAngiotensin-Converting Enzyme 2Antiviral AgentsAptamers, NucleotideBase SequenceCOVID-19HEK293 CellsHumansProtein Interaction Domains and MotifsProtein Interaction MapsSARS-CoV-2Spike Glycoprotein, CoronavirusACE2 protein, humanAngiotensin-Converting Enzyme 2Antiviral AgentsAptamers, NucleotideSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2aptamersCOVID-19receptor-binding domain (RBD)SARS-CoV-2virus neutralization

Identifiers

PMID33684258
PMCPMC8250721

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.