[PSB0739 inhibits formation of semen-derived amyloid fibril]

Yan Lan1, Zichao Yang1, Han Liu1

  • 1School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China.

Abstract

Insights

PSB0739 effectively inhibits the formation of semen-derived amyloid fibrils (SEVI) in a dose-dependent manner. This compound also demonstrates antiviral activity against HIV-1, with no significant cytotoxicity observed in Hela cells at tested concentrations.

Area of Science:

  • Biochemistry
  • Virology
  • Materials Science

Background:

  • Semen-derived amyloid fibrils (SEVI) are implicated in enhancing HIV-1 transmission.
  • Understanding inhibitors of SEVI formation is crucial for developing novel prevention strategies.

Purpose of the Study:

  • To investigate the inhibitory effect of PSB0739 on the formation of SEVI.
  • To evaluate the antiviral activity and cytotoxicity of PSB0739.

Main Methods:

  • Congo red staining and transmission electron microscopy were used to assess SEVI fibril formation.
  • Virus infection assays and Zeta potential measurements evaluated the impact of PSB0739 on SEVI and HIV-1.
  • MTT assays determined the cytotoxicity of PSB0739 in Hela cells.

Main Results:

  • PSB0739 inhibited SEVI fibril formation in a dose-dependent manner.
  • Transmission electron microscopy confirmed that PSB0739 prevented fibril assembly.
  • PSB0739 antagonized SEVI-mediated enhancement of HIV-1 infection and showed direct anti-HIV activity (IC50 = 21.77±5.15 μmol/L).
  • No significant cytotoxicity was observed at concentrations below 62.5 μmol/L.

Conclusions:

  • PSB0739 is an effective inhibitor of semen-derived amyloid fibril formation in vitro.
  • PSB0739 exhibits potential as an antiviral agent against HIV-1, with a favorable safety profile.

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