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Book Chapter: In Vitro Chromatin Assembly: Strategies and Quality Control

TitleIn Vitro Chromatin Assembly: Strategies and Quality Control
Authors
KeywordsAnalytical ultracentrifugation
Atomic force microscopy
Fluorescence labeling
Histone
Micrococcal nuclease digestion
Native polyacrylamide gel electrophoresis
Nucleosomal array
Nucleosome
SEC-MALS
Small-angle X-ray scattering
Issue Date2016
Citation
In Vitro Chromatin Assembly: Strategies and Quality Control. In Marmorstein, R (Ed.), Enzymes of Epigenetics, Part A, p. 3-41. Amsterdam: Elsevier/Academic Press, 2016 How to Cite?
AbstractChromatin accessibility is modulated by structural transitions that provide timely access to the genetic and epigenetic information during many essential nuclear processes. These transitions are orchestrated by regulatory proteins that coordinate intricate structural modifications and signaling pathways. In vitro reconstituted chromatin samples from defined components are instrumental in defining the mechanistic details of such processes. The bottleneck to appropriate in vitro analysis is the production of high quality, and quality-controlled, chromatin substrates. In this chapter, we describe methods for in vitro chromatin reconstitution and quality control. We highlight the strengths and weaknesses of various approaches and emphasize quality control steps that ensure reconstitution of a bona fide homogenous chromatin preparation. This is essential for optimal reproducibility and reliability of ensuing experiments using chromatin substrates.
Persistent Identifierhttp://hdl.handle.net/10722/313354
ISBN
ISSN
2021 Impact Factor: 1.682
2023 SCImago Journal Rankings: 0.133
PubMed Central ID
ISI Accession Number ID
Series/Report no.Methods in Enzymology ; 573

 

DC FieldValueLanguage
dc.contributor.authorMuthurajan, U.-
dc.contributor.authorMattiroli, F.-
dc.contributor.authorBergeron, S.-
dc.contributor.authorZhou, K.-
dc.contributor.authorGu, Y.-
dc.contributor.authorChakravarthy, S.-
dc.contributor.authorDyer, P.-
dc.contributor.authorIrving, T.-
dc.contributor.authorLuger, K.-
dc.date.accessioned2022-06-13T04:17:33Z-
dc.date.available2022-06-13T04:17:33Z-
dc.date.issued2016-
dc.identifier.citationIn Vitro Chromatin Assembly: Strategies and Quality Control. In Marmorstein, R (Ed.), Enzymes of Epigenetics, Part A, p. 3-41. Amsterdam: Elsevier/Academic Press, 2016-
dc.identifier.isbn9780128053652-
dc.identifier.issn0076-6879-
dc.identifier.urihttp://hdl.handle.net/10722/313354-
dc.description.abstractChromatin accessibility is modulated by structural transitions that provide timely access to the genetic and epigenetic information during many essential nuclear processes. These transitions are orchestrated by regulatory proteins that coordinate intricate structural modifications and signaling pathways. In vitro reconstituted chromatin samples from defined components are instrumental in defining the mechanistic details of such processes. The bottleneck to appropriate in vitro analysis is the production of high quality, and quality-controlled, chromatin substrates. In this chapter, we describe methods for in vitro chromatin reconstitution and quality control. We highlight the strengths and weaknesses of various approaches and emphasize quality control steps that ensure reconstitution of a bona fide homogenous chromatin preparation. This is essential for optimal reproducibility and reliability of ensuing experiments using chromatin substrates.-
dc.languageeng-
dc.relation.ispartofEnzymes of Epigenetics-
dc.relation.ispartofseriesMethods in Enzymology ; 573-
dc.subjectAnalytical ultracentrifugation-
dc.subjectAtomic force microscopy-
dc.subjectFluorescence labeling-
dc.subjectHistone-
dc.subjectMicrococcal nuclease digestion-
dc.subjectNative polyacrylamide gel electrophoresis-
dc.subjectNucleosomal array-
dc.subjectNucleosome-
dc.subjectSEC-MALS-
dc.subjectSmall-angle X-ray scattering-
dc.titleIn Vitro Chromatin Assembly: Strategies and Quality Control-
dc.typeBook_Chapter-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/bs.mie.2016.01.002-
dc.identifier.pmid27372747-
dc.identifier.pmcidPMC5098222-
dc.identifier.scopuseid_2-s2.0-84976388653-
dc.identifier.volume573-
dc.identifier.spage3-
dc.identifier.epage41-
dc.identifier.eissn1557-7988-
dc.identifier.isiWOS:000382281500002-
dc.publisher.placeAmsterdam-

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