Prenylation of HDAg and Antiviral Drug Development

Author(s):  
J. S. Glenn
Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2157
Author(s):  
Norbert Odolczyk ◽  
Ewa Marzec ◽  
Maria Winiewska-Szajewska ◽  
Jarosław Poznański ◽  
Piotr Zielenkiewicz

Severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) is a positive-strand RNA virus that causes severe respiratory syndrome in humans, which is now referred to as coronavirus disease 2019 (COVID-19). Since December 2019, the new pathogen has rapidly spread globally, with over 65 million cases reported to the beginning of December 2020, including over 1.5 million deaths. Unfortunately, currently, there is no specific and effective treatment for COVID-19. As SARS-CoV-2 relies on its spike proteins (S) to bind to a host cell-surface receptor angiotensin-converting enzyme-2(ACE2), and this interaction is proved to be responsible for entering a virus into host cells, it makes an ideal target for antiviral drug development. In this work, we design three very short peptides based on the ACE2 sequence/structure fragments, which may effectively bind to the receptor-binding domain (RBD) of S protein and may, in turn, disrupt the important virus-host protein–protein interactions, blocking early steps of SARS-CoV-2 infection. Two of our peptides bind to virus protein with affinity in nanomolar range, and as very short peptides have great potential for drug development.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Chia-Lin Liu ◽  
Hui-Chen Hung ◽  
Shou-Chen Lo ◽  
Ching-Hui Chiang ◽  
I-Jung Chen ◽  
...  

2008 ◽  
Vol 3 (6) ◽  
pp. 529-532
Author(s):  
Dimitrios Coutsinos ◽  
Richard Sloan ◽  
Mark A Wainberg

2005 ◽  
Vol 13 (14) ◽  
pp. 4443-4449 ◽  
Author(s):  
Atanu Roy ◽  
Stewart W. Schneller ◽  
Kathy A. Keith ◽  
Caroll B. Hartline ◽  
Earl R. Kern

2015 ◽  
Vol 118 ◽  
pp. 148-158 ◽  
Author(s):  
Dahai Luo ◽  
Subhash G. Vasudevan ◽  
Julien Lescar

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