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1.
Biotechnol J ; 19(6): e2300685, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38900035

ABSTRACT

Recombinant adeno-associated virus (rAAV) is the leading vector for the delivery of gene therapies. However, low viral genome (VG) titers are common and the proportion of "full" capsids containing the therapeutic gene payload can be highly variable. The coordinated molecular design of plasmids encoding viral components and Helper functions remains a major challenge for rAAV manufacturing. Here we present the design of improved Rep/Cap and Helper plasmids for rAAV2/8 production, (i) a Rep/Cap expression vector harboring independently controllable rep and cap genes and (ii) an improved Helper plasmid harboring E4 gene deletion variants. First, an optimized Rep/Cap vector utilized a truncated p5 promoter, a p5 cis-regulatory element at the 3' end in combination with a heterologous promoter to drive Cap expression and an additional copy of the rep52/40 gene to overexpress short Rep proteins. We demonstrate that Rep78 is essential for efficient rAAV2/8 production in HEK293 cells, and a higher ratio of short Rep to long Rep proteins enhances genome packaging. Second, we identified regulators and open reading frames within the Helper plasmid that contribute to increased rAAV2/8 production. While L4-33k/22k is integral to optimal production, the use of E4orf6-6/7 subset significantly enhanced VG titer. Together, an optimal combination of engineered Rep/Cap and Helper plasmid variants increased VG titer by 3.1-fold. This study demonstrates that configuring and controlling the expression of the different AAV genetic elements contributes toward high rAAV production and product quality (full/empty capsid ratio).


Subject(s)
Dependovirus , Genetic Vectors , Dependovirus/genetics , HEK293 Cells , Humans , Genetic Vectors/genetics , Plasmids/genetics , Promoter Regions, Genetic/genetics , Genome, Viral/genetics , Viral Proteins/genetics
2.
Meas Sci Technol ; 27(8): 084012, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27499587

ABSTRACT

Obtaining pressure field data from particle image velocimetry (PIV) is an attractive technique in fluid dynamics due to its noninvasive nature. The application of this technique generally involves integrating the pressure gradient or solving the pressure Poisson equation using a velocity field measured with PIV. However, very little research has been done to investigate the dynamics of error propagation from PIV-based velocity measurements to the pressure field calculation. Rather than measure the error through experiment, we investigate the dynamics of the error propagation by examining the Poisson equation directly. We analytically quantify the error bound in the pressure field, and are able to illustrate the mathematical roots of why and how the Poisson equation based pressure calculation propagates error from the PIV data. The results show that the error depends on the shape and type of boundary conditions, the dimensions of the flow domain, and the flow type.

3.
Phys Rev Lett ; 106(24): 244501, 2011 Jun 17.
Article in English | MEDLINE | ID: mdl-21770573

ABSTRACT

Rigorous upper limits on the vertical heat transport in two-dimensional Rayleigh-Bénard convection between stress-free isothermal boundaries are derived from the Boussinesq approximation of the Navier-Stokes equations. The Nusselt number Nu is bounded in terms of the Rayleigh number Ra according to Nu≤0.2891Ra(5/12) uniformly in the Prandtl number Pr. This scaling challenges some theoretical arguments regarding asymptotic high Rayleigh number heat transport by turbulent convection.

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