No evidence for basigin/CD147 as a direct SARS-CoV-2 spike binding receptor

Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation

(2020) Daniel Wrapp et al.   SCIENCE

Potential Therapeutic Targets and Promising Drugs for Combating SARS‐CoV‐2

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Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein

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SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor

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IL-6: Relevance for immunopathology of SARS-CoV-2

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COVID-19 spike-host cell receptor GRP78 binding site prediction

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Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor

(2020) Jun Lan et al.   NATURE

Virological assessment of hospitalized patients with COVID-2019

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Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV

(2020) Xiuyuan Ou et al.   Nature Communications

Hypertension, Thrombosis, Kidney Failure, and Diabetes: Is COVID-19 an Endothelial Disease? A Comprehensive Evaluation of Clinical and Basic Evidence

(2020) Celestino Sardu et al.   Journal of Clinical Medicine

TMPRSS2 and TMPRSS4 promote SARS-CoV-2 infection of human small intestinal enterocytes

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Distribution of ACE2, CD147, CD26 and other SARS‐CoV‐2 associated molecules in tissues and immune cells in health and in asthma, COPD, obesity, hypertension, and COVID‐19 risk factors

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Endothelial cell dysfunction: a major player in SARS-CoV-2 infection (COVID-19)?

(2020) Alice Huertas et al.   EUROPEAN RESPIRATORY JOURNAL

Gene expression and in situ protein profiling of candidate SARS-CoV-2 receptors in human airway epithelial cells and lung tissue

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Longitudinal analyses reveal immunological misfiring in severe COVID-19

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The MERS-CoV Receptor DPP4 as a Candidate Binding Target of the SARS-CoV-2 Spike

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Molecular basis of the potential interaction of SARS-CoV-2 spike protein to CD147 in COVID-19 associated-lymphopenia

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Optimizing high-yield production of SARS-CoV-2 soluble spike trimers for serology assays

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COVID-19 and Genetic Variants of Protein Involved in the SARS-CoV-2 Entry into the Host Cells

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Resurrection of the ancestral RH5 invasion ligand provides a molecular explanation for the origin of P. falciparum malaria in humans

(2019) Francis Galaway et al.   PLOS BIOLOGY

Middle East respiratory syndrome coronavirus and bat coronavirus HKU9 both can utilize GRP78 for attachment onto host cells

(2018) Hin Chu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Alpha-v–containing integrins are host receptors for thePlasmodium falciparumsporozoite surface protein, TRAP

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CytoML for cross‐platform cytometry data sharing

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The sterol-responsive RNF145 E3 ubiquitin ligase mediates the degradation of HMG-CoA reductase together with gp78 and Hrd1

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Approaches to identify extracellular receptor–ligand interactions

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Carcinoembryonic Antigen-Related Cell Adhesion Molecule 5 Is an Important Surface Attachment Factor That Facilitates Entry of Middle East Respiratory Syndrome Coronavirus

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Basigin (CD147), a multifunctional transmembrane glycoprotein with various binding partners

(2015) Takashi Muramatsu   JOURNAL OF BIOCHEMISTRY

Basigin is a druggable target for host-oriented antimalarial interventions

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Dose-Response Analysis Using R

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Important Functional Roles of Basigin in Thymocyte Development and T cell Activation

(2014) Hui Yao et al.   International Journal of Biological Sciences

RH5-Basigin interaction plays a major role in the host tropism of Plasmodium falciparum

(2013) M. Wanaguru et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A benchmarked protein microarray-based platform for the identification of novel low-affinity extracellular protein interactions

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Avidity-based Extracellular Interaction Screening (AVEXIS) for the Scalable Detection of Low-affinity Extracellular Receptor-Ligand Interactions

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Basigin is a receptor essential for erythrocyte invasion by Plasmodium falciparum

(2011) Cécile Crosnier et al.   NATURE

A rapid and scalable method for selecting recombinant mouse monoclonal antibodies

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Large-scale screening for novel low-affinity extracellular protein interactions

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