Yuzhen Liu, Christopher D McGann, Mary Krebs, Thomas A Perkins, Rose Fields, Conor K Camplisson, Chris Hsu, Shayan Avanessian, Ashley F Tsue, Evan E Kania, David M Shechner, Brian J Beliveau, Devin K. Schweppe
{"title":"DNA O-MAP uncovers the molecular neighborhoods associated with specific genomic loci","authors":"Yuzhen Liu, Christopher D McGann, Mary Krebs, Thomas A Perkins, Rose Fields, Conor K Camplisson, Chris Hsu, Shayan Avanessian, Ashley F Tsue, Evan E Kania, David M Shechner, Brian J Beliveau, Devin K. Schweppe","doi":"10.1101/2024.07.24.604987","DOIUrl":null,"url":null,"abstract":"The accuracy of crucial nuclear processes such as transcription, replication, and repair, depends on the local composition of chromatin and the regulatory proteins that reside there. Understanding these DNA-protein interactions at the level of specific genomic loci has remained challenging due to technical limitations. Here, we introduce a method termed \"DNA O-MAP\", which uses programmable peroxidase-conjugated oligonucleotide probes to biotinylate nearby proteins. We show that DNA O-MAP can be coupled with sample multiplexed quantitative proteomics and next-generation sequencing to quantify DNA-protein and DNA-DNA interactions at specific genomic loci.","PeriodicalId":501213,"journal":{"name":"bioRxiv - Systems Biology","volume":"42 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Systems Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.07.24.604987","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The accuracy of crucial nuclear processes such as transcription, replication, and repair, depends on the local composition of chromatin and the regulatory proteins that reside there. Understanding these DNA-protein interactions at the level of specific genomic loci has remained challenging due to technical limitations. Here, we introduce a method termed "DNA O-MAP", which uses programmable peroxidase-conjugated oligonucleotide probes to biotinylate nearby proteins. We show that DNA O-MAP can be coupled with sample multiplexed quantitative proteomics and next-generation sequencing to quantify DNA-protein and DNA-DNA interactions at specific genomic loci.