Ontology highlight
ABSTRACT:
INSTRUMENT(S): Orbitrap Exploris 480
ORGANISM(S): Homo Sapiens (human) Severe Acute Respiratory Syndrome Coronavirus 2
TISSUE(S): Lung, Epithelial Cell
SUBMITTER: Mehdi Bouhaddou
LAB HEAD: Nevan J. Krogan
PROVIDER: PXD026302 | Pride | 2022-01-20
REPOSITORIES: Pride
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Thorne Lucy G LG Bouhaddou Mehdi M Reuschl Ann-Kathrin AK Zuliani-Alvarez Lorena L Polacco Ben B Pelin Adrian A Batra Jyoti J Whelan Matthew V X MVX Hosmillo Myra M Fossati Andrea A Ragazzini Roberta R Jungreis Irwin I Ummadi Manisha M Rojc Ajda A Turner Jane J Bischof Marie L ML Obernier Kirsten K Braberg Hannes H Soucheray Margaret M Richards Alicia A Chen Kuei-Ho KH Harjai Bhavya B Memon Danish D Hiatt Joseph J Rosales Romel R McGovern Briana L BL Jahun Aminu A Fabius Jacqueline M JM White Kris K Goodfellow Ian G IG Takeuchi Yasu Y Bonfanti Paola P Shokat Kevan K Jura Natalia N Verba Klim K Noursadeghi Mahdad M Beltrao Pedro P Kellis Manolis M Swaney Danielle L DL García-Sastre Adolfo A Jolly Clare C Towers Greg J GJ Krogan Nevan J NJ
Nature 20211223 7897
The emergence of SARS-CoV-2 variants of concern suggests viral adaptation to enhance human-to-human transmission<sup>1,2</sup>. Although much effort has focused on the characterization of changes in the spike protein in variants of concern, mutations outside of spike are likely to contribute to adaptation. Here, using unbiased abundance proteomics, phosphoproteomics, RNA sequencing and viral replication assays, we show that isolates of the Alpha (B.1.1.7) variant<sup>3</sup> suppress innate immu ...[more]