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HuProt enables that understanding of gene regulation and for developing novel therapeutics for diseases.
REQUEST INFOProtein-nucleic acid interactions play a fundamental role in various biological processes, including gene expression, DNA replication, transcription, translation, and RNA processing. These interactions involve proteins binding to nucleic acids, such as DNA or RNA, to regulate their function and activity. Understanding protein-nucleic acid interactions and developing strategies to modulate these interactions hold great promise for advancing our understanding of gene regulation and for developing novel therapeutics for various diseases, including cancer, genetic disorders, and infectious diseases.
In the featured publication below, HuProt™ microarray was used as part of a combined bioinformatics and protein microarray-based strategy to systematically characterize the human protein-DNA interactome. The paper identified 17,718 protein-DNA interactions (PDIs) between 460 DNA motifs predicted to regulate transcription and 4,191 human proteins of various functional classes. Many known PDIs for transcription factors (TFs) were recovered along with a large number of unanticipated PDIs for known TFs, as well as for previously uncharacterized TFs.
Summary
Protein-DNA interactions (PDIs) mediate a broad range of functions essential for cellular differentiation, function, and survival. However, it is still a daunting task to comprehensively identify and profile sequence-specific PDIs in complex genomes. Here, we have used a combined bioinformatics and protein microarray-based strategy to systematically characterize the human protein-DNA interactome. We identified 17,718 PDIs between 460 DNA motifs predicted to regulate transcription and 4,191 human proteins of various functional classes.
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