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Brent L. Iverson

Researcher at University of Texas at Austin

Publications -  181
Citations -  16022

Brent L. Iverson is an academic researcher from University of Texas at Austin. The author has contributed to research in topics: Antibody & Periplasmic space. The author has an hindex of 63, co-authored 177 publications receiving 15013 citations. Previous affiliations of Brent L. Iverson include University of Texas System & Scripps Health.

Papers
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Journal ArticleDOI

Rethinking the term “pi-stacking”

TL;DR: In this paper, the authors review experimental and theoretical literature across several fields and conclude that the terms "pi stacking" and "pi-pi interactions" do not accurately describe the forces that drive association between aromatic molecules of the types most commonly studied in chemistry or biology laboratories.
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Virus-based toolkit for the directed synthesis of magnetic and semiconducting nanowires.

TL;DR: The unique ability to interchange substrate-specific peptides into the linear self-assembled filamentous construct of the M13 virus introduces a material tunability that has not been seen in previous synthetic routes, and provides a genetic toolkit for growing and organizing nanowires from semiconducting and magnetic materials.
Journal ArticleDOI

Display of heterologous proteins on the surface of microorganisms: From the screening of combinatorial libraries to live recombinant vaccines

TL;DR: Cell displaying protein receptors or antibodies are of use for analytical applications and bioseparations, and Expression of antigens on the surface of nonvirulent microorganisms is an attractive approach to the development of high-efficacy recombinant live vaccines.
Journal ArticleDOI

Viral assembly of oriented quantum dot nanowires

TL;DR: Heterostructured nucleation was achieved with a dual-peptide virus engineered to express two distinct peptides within the same viral capsid, representing a genetically controlled biological synthesis route to a semiconductor nanoscale heterostructure.
Patent

Method of expanded porphyrin-oligonucleotide conjugate synthesis

TL;DR: In this paper, a method of incorporating expanded porphyrins, and particularly of incorporating a sapphyrin or a texaphyrin, before, during, or after chemical synthesis of an oligomer to form an expanded Porphyrin-oligonucleotide conjugate, was proposed.