Titlebook: MERS Coronavirus; Methods and Protocol Rahul Vijay Book 2020 Springer Science+Business Media, LLC, part of Springer Nature 2020 SARS-CoV.ME

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Evaluating MERS-CoV Entry Pathways be traced to its adaptable cell entry steps. The virus can bind host-cell carbohydrates as well as proteinaceous receptors. Following receptor interaction, the virus can utilize diverse host proteases for cleavage activation of virus-host cell membrane fusion and subsequent genome delivery. The fus

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Crystallization and Structural Determination of the Receptor-Binding Domain of MERS-CoV Spike Glycop(mAbs) have been determined by X-ray crystallography, providing structural information about receptor recognition and neutralizing mechanisms of mAbs at the atomic level. In this chapter, we describe the purification, crystallization, and structure determination of the MERS-CoV RBD.

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Bacterial Artificial Chromosome-Based Lambda Red Recombination with the I-SceI Homing Endonuclease fs (~30?kb) using unique reverse genetic systems. These reverse genetic systems include targeted recombination, in vitro ligation, vaccinia virus vectors, and bacterial artificial chromosomes (BACs). Quickly after the identification of Middle East respiratory syndrome-CoV (MERS-CoV), both in vitro li

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Deducing the Crystal Structure of MERS-CoV Helicaseexceptionally large RNA genome (~30?kb) and it encodes an essential replicase, the nonstructural protein 13 (nsp13), a member of superfamily 1 helicases. Nsp13 is among the evolutionary most conserved proteins not only in CoVs but also in nidovirales. Thus, it is considered as an important drug targ

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Quantification of the Middle East Respiratory Syndrome-Coronavirus RNA in Tissues by Quantitative Reed deaths had been reported to the World Health Organization. MERS-CoV is a single-stranded RNA virus that belongs to the . family. MERS-CoV infection leads to a variety of clinical outcomes in humans ranging from asymptomatic and mild infection to severe acute lung injury and multi-organ failure an

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