scholarly journals Vertical Scanning Interferometry for Label-Free Detection of Peptide-Antibody Interactions

2019 ◽  
Vol 8 (2) ◽  
pp. 7
Author(s):  
Andrea Palermo ◽  
Richard Thelen ◽  
Laura Weber ◽  
Tobias Foertsch ◽  
Simone Rentschler ◽  
...  

Peptide microarrays are a fast-developing field enabling the mapping of linear epitopes in the immune response to vaccinations or diseases and high throughput studying of protein-protein interactions. In this respect, a rapid label-free measurement of protein layer topographies in the array format is of great interest but is also a great challenge due to the extremely low aspect ratios of the peptide spots. We have demonstrated the potential of vertical scanning interferometry (VSI) for a detailed morphological analysis of peptide arrays and binding antibodies. The VSI technique is shown to scan an array area of 5.1 square millimeters within 3–4 min at a resolution of 1.4 μm lateral and 0.1 nm vertical in the full automation mode. Topographies obtained by VSI do match the one obtained by AFM measurements, demonstrating the accuracy of the technique. A detailed topology of peptide-antibody layers on single spots was measured. Two different measurement regions are distinguished according to the antibody concentration. In the case of weakly diluted serum, the thickness of the antibody layer is independent of the serum dilution and corresponds to the physical thickness of the accumulated antibody layer. In strongly diluted serum, the thickness measured via VSI is linearly proportional to the serum dilution.

2008 ◽  
Vol 80 (12) ◽  
pp. 4651-4658 ◽  
Author(s):  
Anpan Han ◽  
Marc Creus ◽  
Gregor Schürmann ◽  
Vincent Linder ◽  
Thomas R. Ward ◽  
...  

2005 ◽  
Vol 44 (34) ◽  
pp. 5480-5483 ◽  
Author(s):  
Woon-Seok Yeo ◽  
Dal-Hee Min ◽  
Robert W. Hsieh ◽  
Geoffrey L. Greene ◽  
Milan Mrksich

2009 ◽  
Vol 107 (3) ◽  
pp. 1047-1052 ◽  
Author(s):  
T.-W. Lin ◽  
P.-J. Hsieh ◽  
C.-L. Lin ◽  
Y.-Y. Fang ◽  
J.-X. Yang ◽  
...  

2005 ◽  
Vol 117 (34) ◽  
pp. 5616-5619 ◽  
Author(s):  
Woon-Seok Yeo ◽  
Dal-Hee Min ◽  
Robert W. Hsieh ◽  
Geoffrey L. Greene ◽  
Milan Mrksich

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Rommel J. Gestuveo ◽  
Jamie Royle ◽  
Claire L. Donald ◽  
Douglas J. Lamont ◽  
Edward C. Hutchinson ◽  
...  

AbstractThe escalating global prevalence of arboviral diseases emphasizes the need to improve our understanding of their biology. Research in this area has been hindered by the lack of molecular tools for studying virus-mosquito interactions. Here, we develop an Aedes aegypti cell line which stably expresses Zika virus (ZIKV) capsid proteins in order to study virus-vector protein-protein interactions through quantitative label-free proteomics. We identify 157 interactors and show that eight have potentially pro-viral activity during ZIKV infection in mosquito cells. Notably, silencing of transitional endoplasmic reticulum protein TER94 prevents ZIKV capsid degradation and significantly reduces viral replication. Similar results are observed if the TER94 ortholog (VCP) functioning is blocked with inhibitors in human cells. In addition, we show that an E3 ubiquitin-protein ligase, UBR5, mediates the interaction between TER94 and ZIKV capsid. Our study demonstrates a pro-viral function for TER94/VCP during ZIKV infection that is conserved between human and mosquito cells.


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