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Inhibition of HIV Entry by Targeting the Envelope Transmembrane Subunit gp41. | LitMetric

Inhibition of HIV Entry by Targeting the Envelope Transmembrane Subunit gp41.

Curr HIV Res

Department of Microbiology and Immunology, School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, New York, USA.

Published: December 2016

AI Article Synopsis

  • The HIV envelope protein gp41 is a key target for inhibiting HIV entry, but existing treatments like T20 (Fuzeon) face issues like drug resistance and poor absorption.
  • Researchers are exploring various strategies to improve gp41 inhibitors, focusing on peptide modifications, small compounds, and broadly neutralizing antibodies.
  • Despite the challenges posed by the transient exposure of vulnerable protein conformations, advancements in research are enhancing understanding of gp41, aiming for better treatment options.

Article Abstract

Background: The transmembrane subunit of the HIV envelope protein, gp41 is a vulnerable target to inhibit HIV entry. There is one fusion inhibitor T20 (brand name: Fuzeon, generic name: enfuvirtide) available by prescription. However, it has several drawbacks such as a high level of development of drug resistance, a short-half life in vivo, rapid renal clearance, low oral bioavailability, and it is only used as a salvage therapy. Therefore, investigators have been studying a variety of different modalities to attempt to overcome these limitations.

Methods: Comprehensive literature searches were performed on HIV gp41, inhibition mechanisms, and inhibitors. The latest structural information was collected, and multiple inhibition strategies targeting gp41 were reviewed.

Results: Many of the recent advances in inhibitors were peptide-based. Several creative modification strategies have also been performed to improve inhibitory efficacy of peptides and to overcome the drawbacks of T20 treatment. Small compounds have also been an area of intense research. There is a wide variety in development from those identified by virtual screens targeting specific regions of the protein to natural products. Finally, broadly neutralizing antibodies have also been important area of research. The inaccessible nature of the target regions for antibodies is a challenge, however, extensive efforts to develop better neutralizing antibodies are ongoing.

Conclusion: The fusogenic protein, gp41 has been extensively studied as a promising target to inhibit membrane fusion between the virus and target cells. At the same time, it is a challenging target because the vulnerable conformations of the protein are exposed only transiently. However, advances in biochemical, biophysical, structural, and immunological studies are coming together to move the field closer to an understanding of gp41 structure and function that will lead to the development of novel drugs and vaccines.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909398PMC
http://dx.doi.org/10.2174/1570162x14999160224103908DOI Listing

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