Self-Dimerization Induced Proximity Targeting Chimeras (SDIPTAC) Lead to DCAF1 Loss of Function and Inhibition of HIV Replication

DCAF1 is a donut shaped WD40 repeat protein and a substrate receptor of two distinct E3 ligases. In HIV-1 infection, the viral protein Vpr binds to the top surface of DCAF1, changes its substrate specificity to degrade human proteins involved in antiviral activities, enabling HIV-1 to replicate. We hypothesized that artificial top-to-top self-dimerization of DCAF1 could result in DCAF1 loss-of-function and blocking of the Vpr-DCAF1 interaction. We designed and synthesized seven compounds we call SDIPTACs (Self-dimerization Induced Proximity Targeting Chimeras) which artificially induce DCAF1 self-dimerization through the Vpr interaction surface. Interestingly, SDIPTACs C8 and C9, inhibited Vpr-dependent HIV replication in CD4+ T cells. Biophysical data and crystal structures of four DCAF1-SDIPTAC-DCAF1 ternary complexes revealed more details on DCAF1-DCAF1 complex stability, conformation, and their contribution to compound efficacy. Using SDIPTACs with unique mechanism may therefore be an efficient strategy in the development of future therapeutics for HIV infection and other diseases.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-05-18
DOI
https://doi.org/10.1021/acs.jmedchem.6c00126
Primary Topic
Cancer-related Molecular Pathways
Type
article
Field-Weighted Citation Impact
0.00

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article

Self-Dimerization Induced Proximity Targeting Chimeras (SDIPTAC) Lead to DCAF1 Loss of Function and Inhibition of HIV Replication

Taira Kiyota, Zichong Li, Mark F. Mabanglo, Masoud Vedadi et al.
Journal of Medicinal Chemistry
Cancer-related Molecular Pathways
article

Self-Dimerization Induced Proximity Targeting Chimeras (SDIPTAC) Lead to DCAF1 Loss of Function and Inhibition of HIV Replication

Taira Kiyota, Zichong Li, Mark F. Mabanglo, Masoud Vedadi, David Uehling, Ahmed Mamai, Taraneh Hajian, Yusuke Matsui, Justin P. Pogmore, Laurent Hoffer, Jailall Ramnauth, Smriti Srivastava, Fatemeh Taherian, Ahmed Aman, Rima Al-awar, Mahmoud Noureldin, Sarah Tucker, Melanie Ott, Richard Marcellus
article en

Abstract

DCAF1 is a donut shaped WD40 repeat protein and a substrate receptor of two distinct E3 ligases. In HIV-1 infection, the viral protein Vpr binds to the top surface of DCAF1, changes its substrate specificity to degrade human proteins involved in antiviral activities, enabling HIV-1 to replicate. We hypothesized that artificial top-to-top self-dimerization of DCAF1 could result in DCAF1 loss-of-function and blocking of the Vpr-DCAF1 interaction. We designed and synthesized seven compounds we call SDIPTACs (Self-dimerization Induced Proximity Targeting Chimeras) which artificially induce DCAF1 self-dimerization through the Vpr interaction surface. Interestingly, SDIPTACs C8 and C9, inhibited Vpr-dependent HIV replication in CD4+ T cells. Biophysical data and crystal structures of four DCAF1-SDIPTAC-DCAF1 ternary complexes revealed more details on DCAF1-DCAF1 complex stability, conformation, and their contribution to compound efficacy. Using SDIPTACs with unique mechanism may therefore be an efficient strategy in the development of future therapeutics for HIV infection and other diseases.

Journal of Medicinal Chemistry
Ontario Institute for Cancer Research (CA), Gladstone Institutes (US), 3M (United States) (US), University of Toronto (CA), University of California System (US), Chan Zuckerberg Biohub San Francisco (US)
Gladstone Institutes, Roddenberry Foundation, James B. Pendleton Charitable Trust, Government of Ontario, University of California, San Francisco, National Institute on Drug Abuse, National Institute of Allergy and Infectious Diseases
Good health and well-being
Openalex Percentile: Top 6%
Cancer-related Molecular Pathways
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