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Molecular Biophysics
2 Results
- Research ArticleOpen Access
The ganglioside GM1a functions as a coreceptor/attachment factor for dengue virus during infection
Journal of Biological ChemistryVol. 298Issue 11102570Published online: October 6, 2022- Sarala Neomi Tantirimudalige
- Palur Venkata Raghuvamsi
- Kamal Kant Sharma
- Jonathan Chua Wei Bao
- Ganesh S. Anand
- Thorsten Wohland
Cited in Scopus: 0Dengue virus (DENV) is a flavivirus causing an estimated 390 million infections per year around the world. Despite the immense global health and economic impact of this virus, its true receptor(s) for internalization into live cells has not yet been identified, and no successful antivirals or treatments have been isolated to this date. This study aims to improve our understanding of virus entry routes by exploring the sialic acid–based cell surface molecule GM1a and its role in DENV infection. We studied the interaction of the virus with GM1a using fluorescence correlation spectroscopy, fluorescence crosscorrelation spectroscopy, imaging fluorescence correlation spectroscopy, amide hydrogen/deuterium exchange mass spectrometry, and isothermal titration calorimetry. - Research ArticleOpen Access
The N-terminal disease–associated R5L Tau mutation increases microtubule shrinkage rate due to disruption of microtubule-bound Tau patches
Journal of Biological ChemistryVol. 298Issue 11102526Published online: September 23, 2022- Alisa Cario
- Sanjula P. Wickramasinghe
- Elizabeth Rhoades
- Christopher L. Berger
Cited in Scopus: 0Regulation of the neuronal microtubule cytoskeleton is achieved through the coordination of microtubule-associated proteins (MAPs). MAP-Tau, the most abundant MAP in the axon, functions to modulate motor motility, participate in signaling cascades, as well as directly mediate microtubule dynamics. Tau misregulation is associated with a class of neurodegenerative diseases, known as tauopathies, including progressive supranuclear palsy, Pick's disease, and Alzheimer's disease. Many disease-associated mutations in Tau are found in the C-terminal microtubule-binding domain.