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Designing fluorescent peptide sensors with dual specificity for the detection of hiv-1 protease

journal contribution
posted on 2024-11-01, 22:16 authored by Karla-Luise Herpoldt, Arbel Artzy-Schnirman, Andrew ChristoffersonAndrew Christofferson, Adam Makarucha, Roberto de la Rica, Irene YarovskyIrene Yarovsky, Molly Stevens
HIV-1 protease is a key enzyme in the life cycle of HIV/AIDS, as it is responsible for the formation of the mature virus particle. We demonstrate here that phage-display peptides raised against this enzyme can be used as peptide sensors for the detection of HIV-1 protease in a simple, one-pot assay. The presence of the enzyme is detected through an energy transfer between two peptide sensors when simultaneously complexed with the target protein. The multivalent nature of this assay increases the specificity of the detection by requiring all molecules to be interacting in order for there to be a FRET signal. We also perform molecular dynamics simulations to explore the interaction between the protease and the peptides in order to guide the design of these peptide sensors and to understand the mechanisms which cause these simultaneous binding events. This approach aims to facilitate the development of new assays for enzymes that are not dependent on the cleavage of a substrate and do not require multiple washing steps.

History

Journal

Chemistry of Materials

Volume

27

Issue

20

Start page

7187

End page

7195

Total pages

9

Publisher

American Chemical Society

Place published

United States

Language

English

Copyright

© 2015 American Chemical Society

Former Identifier

2006055544

Esploro creation date

2020-06-22

Fedora creation date

2015-10-20

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