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Melanie Koehler

Researcher at Université catholique de Louvain

Publications -  33
Citations -  1003

Melanie Koehler is an academic researcher from Université catholique de Louvain. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 8, co-authored 25 publications receiving 438 citations. Previous affiliations of Melanie Koehler include Johannes Kepler University of Linz.

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Molecular interaction and inhibition of SARS-CoV-2 binding to the ACE2 receptor.

TL;DR: It is demonstrated, both on model surfaces and on living cells, that the receptor binding domain (RBD) serves as the binding interface within the S-glycoprotein with the ACE2 receptor and the kinetic and thermodynamic properties of this binding pocket are extracted.
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A molecular mechanism for Wnt ligand-specific signaling

TL;DR: It is demonstrated that ligand selectivity is conferred by Reck, which mediates Wnt7-specific binding in a Frizzled-independent manner, and the Wnt decoding capacities of vertebrate cells and the functional diversification of Wnt family members are elucidated.
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Initial Step of Virus Entry: Virion Binding to Cell-Surface Glycans

TL;DR: This review provides a detailed overview of the role of glycans in viral infection and highlights experimental approaches to study virus-glycan binding along with specific examples and highlights the development of the atomic force microscope to investigate interactions with glycans at the single-virion level directly on living mammalian cells.
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Combining confocal and atomic force microscopy to quantify single-virus binding to mammalian cell surfaces

TL;DR: Detailed procedures for probing the specific interactions of viruses with living cells are described; these procedures cover tip preparation, cell sample preparation, step-by-step FD-based AFM imaging and data analysis, and should be able to master the entire set of protocols in 1 month.
Posted ContentDOI

Molecular insights into receptor binding energetics and neutralization of SARS-CoV-2 variants

TL;DR: There is a direct link between increased RBD—ACE2 complex stability and the greater transmissibility observed for the variants of concern and insight into the impact of viral mutations on infection-induced immunity is provided.