High-throughput Vector Development

High-throughput vector development is the parallelized design, construction, and evaluation of biological vectors, especially those used to deliver genetic material into cells. It combines automated molecular cloning, vector libraries, scalable production, and quantitative screening to compare features such as cargo sequence, regulatory elements, tropism, expression, and delivery efficiency. Researchers can use reporter assays, sequencing, and cell-based analyses to identify vector designs that perform reliably across target cell types. This approach accelerates gene therapy research, vaccine development, functional genomics, and synthetic biology by reducing iteration time, revealing design-performance relationships, and supporting the selection of safer, more effective delivery systems.

High-throughput Vector Development - Related Videos

Research

JoVE Journal - Medicine

Development of an Alpha-synuclein Based Rat Model for Parkinson's Disease via Stereotactic Injection of a Recombinant Adeno-associated Viral Vector

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Cited by 12 •

2016

This manuscript describes how viral vector-mediated local gene delivery provides an attractive way to express transgenes in the central nervous system. The protocol outlines all crucial steps to perform a viral vector injection in the substantia nigra of the rat to develop a viral vector-based animal model for Parkinson's disease.

High-throughput Screening for Chemical Modulators of Post-transcriptionally Regulated Genes

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2015

Here we describe a cell-based reporter gene assay as a valuable tool to screen chemical libraries for compounds modulating post-transcriptional control mechanisms exerted through 3’ UTR.

Utilizing the Antigen Capsid-Incorporation Strategy for the Development of Adenovirus Serotype 5-Vectored Vaccine Approaches

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Cited by 1 •

2015

Here, we present a protocol to generate a proof-of-principle divalent adenovirus type 5 (Ad5) vector Ad5/H5-HVR1-KWAS-HVR5-His6 by utilizing the Antigen Capsid-Incorporation strategy. This vector was demonstrated to exhibit qualitative fitness, the capability to escape Ad5-positive sera in vitro, and the antigenicity as well as immunogenicity to the incorporated antigens.

High-throughput CRISPR Vector Construction and Characterization of DNA Modifications by Generation of Tomato Hairy Roots

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Cited by 37 •

2016

Using DNA assembly, multiple CRISPR vectors can be constructed in parallel in a single cloning reaction, making the construction of large numbers of CRISPR vectors a simple task. Tomato hairy roots are an excellent model system to validate CRISPR vectors and generate mutant materials.

Use of a High-throughput In Vitro Microfluidic System to Develop Oral Multi-species Biofilms

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Cited by 28 •

2014

The goal of this methods paper is to describe the use of a microfluidic system for the development of multi-species biofilms that contain species typically identified in human supragingival dental plaque. Methods to describe biofilm architecture, biofilm viability, and an approach to harvest biofilm for culture-dependent or culture-independent analyses are highlighted.

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