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Methods in Genetic Engineering

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Louay Hallak

Louay Hallak

Consultant and Advisor for Ohio State University and Nationwide Children’s hospital

Dr. Hallak is a scientist and entrepreneur with interests in molecular biology, gene therapy, and related fields. He serves as an advisor on the boards of two biotechnology companies and a consultant for several institutions including Ohio State University and Nationwide Children’s hospital. His initial work was focused on understanding the mechanisms of negative-strand RNA virus interaction and entry into susceptible cells. This led to the discovery that certain cell-surface anchored carbohydrates play an important role in respiratory syncytial virus attachment and subsequent entry to the cell as opposed to the more common protein-protein interaction route between viral glycoproteins and cell surface receptors. He used this extensive examination of virus-cell interaction and the reverse genetics of negative-strand RNA viruses to design recombinant viral vectors based on the vaccine strain of measles virus for targeting tumors and resulting in the successful creation of one of the first targeted live replicating viral vectors for gene therapy. As a byproduct of working with viral genomes, Dr. Hallak invented URMAC, a set of fast and reliable PCR-based methods for cloning and mutagenesis of large DNA plasmids containing intact viral genomes in vitro. He is an alumnus of Rush University, Chicago, IL, and Mayo Clinic, Rochester, MN.

Collection Overview

The genetic makeup of an organism is the foundation for its existence; as such, naturally occurring changes in this makeup result in evolution, adaptation, diversity, or sometimes genetic defects and disease. Methods and molecular tools used to introduce changes to this genetic makeup (for the purpose of understanding the role of genes and to modulate their functions) have been growing since the discovery and isolation of DNA. This purposeful genetic manipulation has accelerated and emerged as a distinct field of science known as genetic engineering. Therefore, genetic engineering simply refers to genetic modification in process and application. In this collection, we aim to collect relevant process methods such as (1) recombinant DNA and cloning, (2) genome editing, and (3) delivery techniques including viral vectors. Since the application of genetic engineering is ever-expanding in very diverse fields (including medicine, agriculture, and marine biology), we will limit the applications in this collection to gene therapy in medicine. Methods in this collection may include a new approach or modified version of an existing technique that imparts significant improvement(s) such as (1) cost, (2) accuracy, (3) speed, (4) quality, or (5) efficiency. Examples of acceptable methods include: (1) PCR-based technologies (2) DNA mutagenesis and gene editing techniques including traditional site-directed, TALEN, and CRISPR/cas9 (3) introduction of genetic materials into cells, organs, or organisms such as transformation and transduction using chemical, viral or non-viral vectors, and (4) methods identifying new molecular tools or functions such as enzymes, plasmids, probes, and tags.

 

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High-Throughput Metabolic Profiling for Model Refinements of Microalgae
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High-Throughput Metabolic Profiling for Model Refinements of Microalgae

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2021

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