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- Creators: Ira A. Fulton Schools of Engineering
- Resource Type: Text
- Status: Published
Viral protein U (Vpu) is a type-III integral membrane protein encoded by Human Immunodeficiency Virus-1 (HIV- 1). It is expressed in infected host cells and plays several roles in viral progeny escape from infected cells, including down-regulation of CD4 receptors. But key structure/function questions remain regarding the mechanisms by which the Vpu protein contributes to HIV-1 pathogenesis. Here we describe expression of Vpu in bacteria, its purification and characterization. We report the successful expression of PelB-Vpu in Escherichia coli using the leader peptide pectate lyase B (PelB) from Erwinia carotovora. The protein was detergent extractable and could be isolated in a very pure form. We demonstrate that the PelB signal peptide successfully targets Vpu to the cell membranes and inserts it as a type I membrane protein. PelB-Vpu was biophysically characterized by circular dichroism and dynamic light scattering experiments and was shown to be an excellent candidate for elucidating structural models.
Eigenvalues of the 3D critical point equation (∇u)ν = λν are normally computed numerically. In the letter, we present analytic solutions for 3D swirling strength in both compressible and incompressible flows. The solutions expose functional dependencies that cannot be seen in numerical solutions. To illustrate, we study the difference between using fluctuating and total velocity gradient tensors for vortex identification. Results show that mean shear influences vortex detection and that distortion can occur, depending on the strength of mean shear relative to the vorticity at the vortex center.