Microfluidic Low-Input Fluidized-Bed Enabled ChIP-seq Device for Automated and Parallel Analysis of Histone Modifications
Affiliations
Genome-wide epigenetic changes, such as histone modifications, form a critical layer of gene regulations and have been implicated in a number of different disorders such as cancer and inflammation. Progress has been made to decrease the input required by gold-standard genome-wide profiling tools like chromatin immunoprecipitation followed by sequencing (i.e., ChIP-seq) to allow scarce primary tissues of a specific type from patients and lab animals to be tested. However, there has been practically no effort to rapidly increase the throughput of these low-input tools. In this report, we demonstrate LIFE-ChIP-seq (low-input fluidized-bed enabled chromatin immunoprecipitation followed by sequencing), an automated and high-throughput microfluidic platform capable of running multiple sets of ChIP assays on multiple histone marks in as little as 1 h with as few as 50 cells per assay. Our technology will enable testing of a large number of samples and replicates with low-abundance primary samples in the context of precision medicine.
Alexandre L, Araya-Farias M, Nguyen M, Naoumi N, Gropplero G, Gizeli E Microsyst Nanoeng. 2023; 9:109.
PMID: 37680311 PMC: 10480215. DOI: 10.1038/s41378-023-00582-4.
Alexandre L, Bendali A, Pereiro I, Azimani M, Dumas S, Malaquin L Sci Rep. 2022; 12(1):9468.
PMID: 35676309 PMC: 9176165. DOI: 10.1038/s41598-022-13304-z.
nMOWChIP-seq: low-input genome-wide mapping of non-histone targets.
Liu Z, Naler L, Zhu Y, Deng C, Zhang Q, Zhu B NAR Genom Bioinform. 2022; 4(2):lqac030.
PMID: 35402909 PMC: 8988714. DOI: 10.1093/nargab/lqac030.
Joint single-cell multiomic analysis in Wnt3a induced asymmetric stem cell division.
Sun Z, Tang Y, Zhang Y, Fang Y, Jia J, Zeng W Nat Commun. 2021; 12(1):5941.
PMID: 34642323 PMC: 8511096. DOI: 10.1038/s41467-021-26203-0.
Dirks R, Thomas P, Wu H, Jones R, Stunnenberg H, Marks H Genome Res. 2021; 31(5):919-933.
PMID: 33707229 PMC: 8092002. DOI: 10.1101/gr.260745.120.