TY - JOUR
T1 - The Viral protein Corona Directs Viral Pathogenesis and Amyloid Aggregation
AU - Ezzat, Kariem
AU - Pernemalm, Maria
AU - Palsson, Sandra
AU - Roberts, Thomas C.
AU - Jarver, Peter
AU - Dondalska, Aleksandra
AU - Bestas, Burcu
AU - Sobkowiak, Michal J.
AU - Levanen, Bettina
AU - Skold, Magnus
AU - Thompson, Elizabeth A.
AU - Saher, Osama
AU - Kari, Otto K.
AU - Lajunen, Tatu
AU - Ekstrom, Eva Sverremark
AU - Nilsson, Caroline
AU - Ishchenko, Yevheniia
AU - Malm, Tarja
AU - Wood, Matthew J.A.
AU - Power, Ultan
AU - Masich, Sergej
AU - Linden, Anders
AU - Sandberg, Johan K.
AU - Lehtio, Janne
AU - Spetz, Anna-Lena
AU - Andaloussi, Samir EL
PY - 2019/5/27
Y1 - 2019/5/27
N2 - Artificial nanoparticles accumulate a protein corona layer in biological fluids, which significantly influences their bioactivity. As nanosized obligate intracellular parasites, viruses share many biophysical properties with artificial nanoparticles in extracellular environments and here we show that respiratory syncytial virus (RSV) and herpes simplex virus 1 (HSV-1) accumulate a rich and distinctive protein corona in different biological fluids. Moreover, we show that corona pre-coating differentially affects viral infectivity and immune cell activation. Additionally, we demonstrate that viruses bind amyloidogenic peptides in their corona and catalyze amyloid formation via surface-assisted heterogeneous nucleation. Importantly, we show that HSV-1 catalyzes the aggregation of the amyloid beta peptide (Aβ42), a major constituent of amyloid plaques in Alzheimer's disease, in-vitro and in animal models. Our results highlight the viral protein corona as an acquired structural layer that is critical for viral-host interactions and illustrate a mechanistic convergence between viral and amyloid pathologies.
AB - Artificial nanoparticles accumulate a protein corona layer in biological fluids, which significantly influences their bioactivity. As nanosized obligate intracellular parasites, viruses share many biophysical properties with artificial nanoparticles in extracellular environments and here we show that respiratory syncytial virus (RSV) and herpes simplex virus 1 (HSV-1) accumulate a rich and distinctive protein corona in different biological fluids. Moreover, we show that corona pre-coating differentially affects viral infectivity and immune cell activation. Additionally, we demonstrate that viruses bind amyloidogenic peptides in their corona and catalyze amyloid formation via surface-assisted heterogeneous nucleation. Importantly, we show that HSV-1 catalyzes the aggregation of the amyloid beta peptide (Aβ42), a major constituent of amyloid plaques in Alzheimer's disease, in-vitro and in animal models. Our results highlight the viral protein corona as an acquired structural layer that is critical for viral-host interactions and illustrate a mechanistic convergence between viral and amyloid pathologies.
U2 - 10.1038/s41467-019-10192-2
DO - 10.1038/s41467-019-10192-2
M3 - Article
SN - 2041-1723
VL - 10
JO - Nature Communications
JF - Nature Communications
M1 - 2331
ER -