Human respiratory syncytial virus (RSV) is a major cause of severe lower respiratory tract infection in infants, immunocompromised patients, and the elderly. The RSV fusion (F) protein mediates fusion of the viral envelope with the target cell membrane during virus entry and is a primary target for antiviral drug and vaccine development. The F protein contains two heptad repeat regions, HR1 and HR2. Peptides corresponding to these regions form a six-helix bundle structure that is thought to play a critical role in membrane fusion. However, characterization of six-helix bundle formation in native RSV F protein has been hindered by the fact that a trigger for F protein conformational change has yet to be identified. Here we demonstrate that RSV F protein on the surface of infected cells undergoes a conformational change following exposure to elevated temperature, resulting in the formation of the six-helix bundle structure. We first generated and characterized six-helix bundle-specific antibodies raised against recombinant peptides modeling the RSV F protein six-helix bundle structure. We then used these antibodies as probes to monitor RSV F protein six-helix bundle formation in response to a diverse array of potential triggers of conformational changes. We found that exposure of 'membrane-anchored' RSV F protein to elevated temperature (45-55 degrees C) was sufficient to trigger six-helix bundle formation. Antibody binding to the six-helix bundle conformation was detected by both flow cytometry and cell-surface immunoprecipitation of the RSV F protein. None of the other treatments, including interaction with a number of potential receptors, resulted in significant binding by six-helix bundle-specific antibodies. We conclude that native, untriggered RSV F protein exists in a metastable state that can be converted in vitro to the more stable, fusogenic six-helix bundle conformation by an increase in thermal energy. These findings help to better define the mechanism of RSV F-mediated membrane fusion and have important implications for the identification of therapeutic strategies and vaccines targeting RSV F protein conformational changes.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789909PMC
http://dx.doi.org/10.1016/j.virol.2009.10.040DOI Listing

Publication Analysis

Top Keywords

six-helix bundle
36
rsv protein
32
bundle formation
16
elevated temperature
12
protein
12
protein six-helix
12
bundle structure
12
six-helix
11
rsv
11
bundle
9

Similar Publications

A DNA Origami Pivot Hinge Driven by DNA Intercalators.

ACS Nano

December 2024

Department of Mechanical Engineering, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Korea.

Article Synopsis
  • The DNA origami technique allows for the creation of nanoscale structures that can change shape dynamically.
  • A new design features a hinge mechanism that pivots based on the concentration of DNA intercalators, using gold nanoparticles for support.
  • This pivoting motion can be adjusted and repeated, potentially leading to the development of advanced nanosensors and actuators that amplify tiny movements caused by molecular interactions.
View Article and Find Full Text PDF

Protein mimics of fusion core from SARS-CoV-1 can inhibit SARS-CoV-2 entry.

Biochem Biophys Res Commun

December 2024

Key Laboratory of Virology and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, 430207, China; University of Chinese Academy of Sciences, Beijing, 100049, China; Hubei Jiangxia Laboratory, Wuhan, Hubei, 430200, China. Electronic address:

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a member of the genus Betacoronavirus (subgenus Sarbecovirus) and shares significant genomic and phylogenetic similarities with severe acute respiratory syndrome coronavirus 1 (SARS-CoV-1). SARS-CoV-2 infection occurs through membrane fusion between the virus and host cell membranes, which is facilitated by the spike glycoprotein subunit 2 (S2). The folding of three heptad-repeat regions 1 (HR1) into a central trimeric core structure, along with the binding of three heptad-repeat regions 2 (HR2) in an antiparallel manner within the groove formed between the HR1 regions, which provides the driving force for membrane fusion.

View Article and Find Full Text PDF

Cryo-EM structure and polar assembly of the PS2 S-layer of .

bioRxiv

September 2024

Structural and Molecular Microbiology, VIB-VUB Center for Structural Biology, VIB, Pleinlaan 2, 1050 Brussels, Belgium.

Article Synopsis
  • - The study focuses on Corynebacteriales, which have a unique outer membrane structure made of mycolic acids, and explores the mysterious 'S-layer' that enhances this membrane.
  • - Researchers isolated the PS2 S-layer and used advanced 3D cryoEM techniques to reveal its structure, consisting of hexameric core units and trimeric lattice arrangements that contribute to a semipermeable membrane.
  • - The findings provide insights into S-layer functions and evolution within Corynebacteriales, suggesting potential for developing bioengineered materials that utilize these membrane properties.
View Article and Find Full Text PDF

Alpaca-derived nanobody targeting the hydrophobic pocket of the HIV-1 gp41 NHR broadly neutralizes HIV-1 by blocking six-helix bundle formation.

Curr Res Microb Sci

July 2024

Shanghai Institute of Infectious Disease and Biosecurity, Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS), School of Basic Medical Sciences, Shanghai Frontiers Science Center of Pathogenic Microbes and Infection, Fudan University, Shanghai, China.

Article Synopsis
  • The hydrophobic pocket of HIV-1 gp41 NHR is essential for forming a six-helix bundle during viral fusion, making it a prime target for drug design.
  • However, the size of traditional antibodies like IgG prevents them from fitting into this pocket during the crucial fusion process.
  • Nanobodies (Nbs), specifically Nb-172, have been developed to target this region and show promising neutralizing effects against various HIV-1 strains, suggesting their potential as a therapeutic option.
View Article and Find Full Text PDF

ADS-J21 is a novel HIV-1 entry inhibitor targeting gp41.

Curr Res Microb Sci

July 2024

Hebei Key Laboratory of Analysis and Control of Zoonotic Pathogenic Microorganism, College of Life Sciences, Hebei Agricultural University, Baoding, 071001, China.

Article Synopsis
  • HIV-1 envelope glycoprotein gp41 is crucial for the virus to fuse with host cells, making it a target for anti-HIV drugs.
  • A new compound named ADS-J21 has been developed, which shares a similar Y-shaped structure with the previously studied ADS-J1 but has a lower molecular weight and shows effective activity against various HIV-1 strains.
  • Research showed that ADS-J21 works by blocking the formation of a critical structure (the six-helix bundle) in gp41, paving the way for it to be optimized as a small-molecule fusion inhibitor.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!