Luke Erber

Assistant Professor

University of Kansas

United States

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Dr. Luke Erber is an Assistant Professor at the University of Kansas, USA. His research focuses on DNA-protein interactions, cellular metabolite effects on genome stability, and proteomic analyses related to environmental exposures and neuronal responses. Recent publications include studies on the repair of DNA-protein crosslinks and the effects of endogenous metabolites on cellular processes.

Articles (14)

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2025

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2021

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2020

Collaborators (11)

Anja Bielinsky

Professor and Chair

University of Virginia

UNITED STATES

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Ivan Rusyn

UNITED STATES

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Gunnar Boysen

Associate Professor -tenured

UNITED STATES

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Lisa Peterson

University of Minnesota

UNITED STATES

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Suresh Pujari

University of Minnesota

UNITED STATES

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Zhipeng Wang

Assistant Professor

Sylvester Comprehensive Cancer Center

UNITED STATES

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Yue Chen

University of Minnesota

UNITED STATES

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Phu V. Tran

University of Minnesota

UNITED STATES

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Natalia Y. Tretyakova

University of Minnesota

UNITED STATES

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James J. Galligan

UNITED STATES

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Scott Walmsley

University of Minnesota

UNITED STATES

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Luke Erber

Research Interests

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About

Articles (14)

BPTF Target Engagement by Acetylated H2A.Z Photoaffinity Probes

Improved detection of DNA replication fork-associated proteins

Endogenous Cellular Metabolite Methylglyoxal Induces DNA–Protein Cross-Links in Living Cells

SPRTN metalloprotease participates in repair of ROS-mediated DNA-protein crosslinks

Endogenous Metabolites and Genome Instability in Aging and Disease

HypDB

Quantitative Proteome and Transcriptome Dynamics Analysis Reveals Iron Deficiency Response Networks and Signature in Neuronal Cells

Effects of GSTT1 Genotype on the Detoxification of 1,3-Butadiene Derived Diepoxide and Formation of Promutagenic DNA–DNA Cross-Links in Human Hapmap Cell Lines

Site-Specific 5-Formyl Cytosine Mediated DNA-Histone Cross-Links

Proteome-Wide Profiling of Cellular Targets Modified by Dopamine Metabolites Using a Bio-Orthogonally Functionalized Catecholamine

Quantitative NanoLC/NSI<sup>+</sup>-HRMS Method for 1,3-Butadiene Induced <i>bis</i>-N7-guanine DNA-DNA Cross-Links in Urine

Iron Deficiency Reprograms Phosphorylation Signaling and Reduces O-GlcNAc Pathways in Neuronal Cells

Intra- and Inter-Species Variability in Urinary N7-(1-Hydroxy-3-buten-2-yl)guanine Adducts Following Inhalation Exposure to 1,3-Butadiene

Characterizing Adduct Formation of Electrophilic Skin Allergens with Human Serum Albumin and Hemoglobin

Collaborators (11)

Anja Bielinsky

Ivan Rusyn

Gunnar Boysen

Lisa Peterson

Suresh Pujari

Zhipeng Wang

Yue Chen

Phu V. Tran

Natalia Y. Tretyakova

James J. Galligan

Scott Walmsley

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