Scot O

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Associate Professor

University of Nebraska Medical Center

United States

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Recent Grants

Grant: Close

Role of the Clp Protease Systems in the Growth and Pathogenesis of Chlamydia

Open Date: 2020-09-01

Close Date: 2021-08-31

Grant: Close

Development of Tools for Conditional Knockouts in Chlamydia

Open Date: 2019-07-01

Close Date: 2021-06-30

Grant: Close

Regulatory Role of Tandem Tryptophan Codons in Chlamydial Persistence

Open Date: 2019-02-08

Close Date: 2024-01-31

Grant: Close

Collaborative Research: Mechanism of Polarized Budding in Chlamydia

Open Date: 2018-08-15

Close Date: 2021-07-31

Grant: Close

CAREER: Effects of Reductive Evolution on Amino Acid Stress Responses in Bacteria

Open Date: 2017-10-26

Close Date: 2022-06-30

Articles (13)

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2021

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2021

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University of Nebraska Medical Center

UNITED STATES

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Scot O

Research Interests

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Recent Grants

Articles (13)

Metabolic model guided CRISPRi identifies a central role for phosphoglycerate mutase in Chlamydia trachomatis persistence

Targeted repression of topA by CRISPRi reveals a critical function for balanced DNA topoisomerase I activity in the Chlamydia trachomatis developmental cycle

Molecular Characterization of the ClpC AAA+ ATPase in the Biology of Chlamydia trachomatis

The Periplasmic Tail-Specific Protease, Tsp, Is Essential for Secondary Differentiation in <i>Chlamydia trachomatis</i>.

The Unique N-Terminal Domain of Chlamydial Bactofilin Mediates Its Membrane Localization and Ring-Forming Properties

Tryptophan Availability during Persistence of Chlamydia trachomatis Directly Impacts Expression of Chlamydial Cell Division Proteins

Identification of the alternative sigma factor regulons of Chlamydia trachomatis using multiplexed CRISPR interference

The structure of caseinolytic protease subunit ClpP2 reveals a functional model of the caseinolytic protease system from Chlamydia trachomatis

Tag-Dependent Substrate Selection of ClpX Underlies Secondary Differentiation of Chlamydia trachomatis

A Dynamic, Ring-Forming Bactofilin Critical for Maintaining Cell Size in the Obligate Intracellular Bacterium Chlamydia trachomatis

Codon-Dependent Transcriptional Changes in Response to Tryptophan Limitation in the Tryptophan Auxotrophic Pathogens Chlamydia trachomatis and Streptococcus pyogenes

CRISPR Interference To Inducibly Repress Gene Expression in Chlamydia trachomatis

Inclusion Membrane Growth and Composition Are Altered by Overexpression of Specific Inclusion Membrane Proteins in Chlamydia trachomatis L2

Collaborators (5)

Rajib Saha

Nicholas Wood

Derek Fisher

George Liechti

REY CARABEO

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