Macromolecular Crowding and DNA: Bridging the Gap between In Vitro and In Vivo.

DNA bovine serum albumin (BSA) dextran liquid–liquid phase separation (LLPS) macromolecular crowding polyethylene glycol (PEG)

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
15 Dec 2023
Historique:
received: 13 09 2023
revised: 29 11 2023
accepted: 05 12 2023
medline: 23 12 2023
pubmed: 23 12 2023
entrez: 23 12 2023
Statut: epublish

Résumé

The cellular environment is highly crowded, with up to 40% of the volume fraction of the cell occupied by various macromolecules. Most laboratory experiments take place in dilute buffer solutions; by adding various synthetic or organic macromolecules, researchers have begun to bridge the gap between in vitro and in vivo measurements. This is a review of the reported effects of macromolecular crowding on the compaction and extension of DNA, the effect of macromolecular crowding on DNA kinetics, and protein-DNA interactions. Theoretical models related to macromolecular crowding and DNA are briefly reviewed. Gaps in the literature, including the use of biologically relevant crowders, simultaneous use of multi-sized crowders, empirical connections between macromolecular crowding and liquid-liquid phase separation of nucleic materials are discussed.

Identifiants

pubmed: 38139331
pii: ijms242417502
doi: 10.3390/ijms242417502
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : R35GM149296
Pays : United States

Auteurs

Dylan Collette (D)

Department of Physics, College of Arts & Sciences, Emory University, Atlanta, GA 30322, USA.

David Dunlap (D)

Department of Physics, College of Arts & Sciences, Emory University, Atlanta, GA 30322, USA.

Laura Finzi (L)

Department of Physics, College of Arts & Sciences, Emory University, Atlanta, GA 30322, USA.

Classifications MeSH