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Current Research Methods for the Study of Histones

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Valerie Carabetta

Valerie Carabetta

Cooper Medical School of Rowan University

Dr. Valerie Carabetta joined Cooper Medical School of Rowan University in 2018, where she educates medical students in microbiology and infectious disease. She earned her PhD from Princeton University in Molecular Biology and completed her post-doctoral research at the Public Health Research Institute, New Jersey Medical School (Rutgers University). The overarching theme of her research program is combatting antimicrobial resistance in bacteria, either by performing the basic research needed to design novel therapeutics, designing new strategies to combat infections or studying the mechanisms of resistance. One of her interests involves understanding the physiological consequences of protein acetylation in bacteria, and the underlying mechanisms that control it. Recently, Ne-lysine acetylation was realized to be a prevalent bacterial post-translational modification (PTM), contrary to the historical notion that this was a rare occurrence. Her focus is on understanding the biological consequences of the acetylation of a histone-like protein in bacteria. To study these histone-like proteins, she uses molecular genetics, biochemistry, and mass spectrometry-based techniques. With proper study, the enzymes involved in regulation (i.e. acetylases and deacetylases) or the acetylated form of a key protein (i.e. virulence factors, essential genes, etc.) may provide valuable, druggable targets.

Collection Overview

In living cells, meters of DNA must be significantly compacted to fit inside of the tiny compartment in the cell. In eukaryotic cells, the first level of chromosomal compaction occurs by wrapping the DNA around nucleosomes, which are comprised of histone proteins. The histone proteins are important regulatory proteins, as they are involved in the control of DNA replication, recombination, repair and importantly, gene expression. They contain long, highly basic, unstructured N-terminal tails, which are the sites of various post-translational modifications (PTMs). There are ~20 different PTMs that have been identified and described so far, including lysine acylation, phosphorylation, methylation, and ubiquitination. Interestingly, histones and histone-like proteins (functional homologs) have been identified in all domains of life, including the archaea and eubacteria. Many regulatory functions, and even some PTMs are evolutionarily conserved. Histones were initially discovered and identified in the 1880’s, and now there are many techniques available for histone purification and characterization. With the advances in mass spectrometry technology, mapping of PTMs with site specific resolution and determination of stoichiometry have become possible. In addition, new techniques to study chromosome structure and architecture allows for advanced DNA binding studies of histones. The purpose of this methods collection is to create a comprehensive guide on the most up-to-date protocols for purification and functional characterization of histones and histone-like proteins, and to describe new methodologies for studying DNA-histone interactions.

Articles

Identification of Modified Histones as Binding Substrates of Human Spindlin Family Member 4 (SPIN4) by Peptide Arrays and Native Nucleosome Pulldown
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Identification of Modified Histones as Binding Substrates of Human Spindlin Family Member 4 (SPIN4) by Peptide Arrays and Native Nucleosome Pulldown

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