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A Bimodal Nanosensor for Probing Influenza Fusion Protein Activity Using Magnetic Relaxation.
Jain, Vedant; Shelby, Tyler; Patel, Truptiben; Mekhedov, Elena; Petersen, Jennifer D; Zimmerberg, Joshua; Ranaweera, Ahinsa; Weliky, David P; Dandawate, Prasad; Anant, Shrikant; Sulthana, Shoukath; Vasquez, Yolanda; Banerjee, Tuhina; Santra, Santimukul.
Afiliación
  • Jain V; Department of Chemistry, Pittsburg State University, Pittsburg, Kansas 66762, United States.
  • Shelby T; Department of Chemistry, Pittsburg State University, Pittsburg, Kansas 66762, United States.
  • Patel T; Department of Chemistry, Pittsburg State University, Pittsburg, Kansas 66762, United States.
  • Mekhedov E; Section on Integrative Biophysics, Division of Basic and Translational Biophysics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, United States.
  • Petersen JD; Section on Integrative Biophysics, Division of Basic and Translational Biophysics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, United States.
  • Zimmerberg J; Section on Integrative Biophysics, Division of Basic and Translational Biophysics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, United States.
  • Ranaweera A; Department of Chemistry, Michigan State University, East Lansing, Michigan 48824, United States.
  • Weliky DP; Department of Chemistry, Michigan State University, East Lansing, Michigan 48824, United States.
  • Dandawate P; Department of Molecular and Integrative Physiology and Department of Surgery, The University of Kansas Medical Center, Kansas City, Kansas 66160, United States.
  • Anant S; Department of Molecular and Integrative Physiology and Department of Surgery, The University of Kansas Medical Center, Kansas City, Kansas 66160, United States.
  • Sulthana S; Department of Chemistry, Oklahoma State University, Stillwater, Oklahoma 74078, United States.
  • Vasquez Y; Department of Chemistry, Oklahoma State University, Stillwater, Oklahoma 74078, United States.
  • Banerjee T; Department of Chemistry, Pittsburg State University, Pittsburg, Kansas 66762, United States.
  • Santra S; Department of Chemistry, Pittsburg State University, Pittsburg, Kansas 66762, United States.
ACS Sens ; 6(5): 1899-1909, 2021 05 28.
Article en En | MEDLINE | ID: mdl-33905237
ABSTRACT
Viral fusion is a critical step in the entry pathway of enveloped viruses and remains a viable target for antiviral exploration. The current approaches for studying fusion mechanisms include ensemble fusion assays, high-resolution cryo-TEM, and single-molecule fluorescence-based methods. While these methods have provided invaluable insights into the dynamic events underlying fusion processes, they come with their own limitations. These often include extensive data and image analysis in addition to experimental time and technical requirements. This work proposes the use of the spin-spin T2 relaxation technique as a sensitive bioanalytical method for the rapid quantification of interactions between viral fusion proteins and lipids in real time. In this study, new liposome-coated iron oxide nanosensors (LIONs), which mimic as magnetic-labeled host membranes, are reported to detect minute interactions occurring between the membrane and influenza's fusion glycoprotein, hemagglutinin (HA). The influenza fusion protein's interaction with the LION membrane is detected by measuring changes in the sensitive spin-spin T2 magnetic relaxation time using a bench-top NMR instrument. More data is gleaned from including the fluorescent dye DiI into the LION membrane. In addition, the effects of environmental factors on protein-lipid interaction that affect fusion such as pH, time of incubation, trypsin, and cholesterol were also examined. Furthermore, the efficacy and sensitivity of the spin-spin T2 relaxation assay in quantifying similar protein/lipid interactions with more native configurations of HA were demonstrated using virus-like particles (VLPs). Shorter domains derived from HA were used to start a reductionist path to identify the parts of HA responsible for the NMR changes observed. Finally, the known fusion inhibitor Arbidol was employed in our spin-spin T2 relaxation-based fusion assay to demonstrate the application of LIONs in real-time monitoring of this aspect of fusion for evaluation of potential fusion inhibitors.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Gripe Humana Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: ACS Sens Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Gripe Humana Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: ACS Sens Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos