Interaction of deoxyribonucleic acid with deoxyribonucleic acid-binding protein from starved cells: cluster formation and crystal growing as a model of initial stages of nucleoid biocrystallization.
Eduard TereshkinKsenia TereshkinaNatalia LoikoAlexei ChulichkovVladislav KovalenkoYurii KrupyanskiiPublished in: Journal of biomolecular structure & dynamics (2018)
The paper represents the study of interaction between deoxyribonucleic acid (DNA) and deoxyribonucleic acid-binding protein from starved cells (DPS) cluster formation and crystal growing within a cell. This study is a part of the project that includes European Synchrotron Radiation Facility (ESRF) investigations of in vivo and in vitro nanocrystallization processes of Escherichia coli (E. coli) nucleoid under stress condition combined with theoretical molecular dynamics approaches. Nucleoid biocrystallization is an adaptive mechanism of bacterial cells under stress. It is poorly understood at the present time. Understanding crystal formation process is a very important for molecular biology, pharmacology and other areas. In the simulation part the coarse-grained modeling of various combinations of the following molecules was used: DPS proteins (from 1 to 108 DPS dodecamers in simulation box), short DNA fragments with a length of 24 base pairs (b.p., from 1 to 100 DNA fragments in simulation box) and a part of pBluescript SK(+) plasmide with a length of 161 b.p., in the presence of ions. We defined structural, energetic and dynamic properties of DPS-DPS and DPS-DNA complexes in clusters and crystals that allow us to predict crystal formation and the structure of these crystals in experimental systems. Communicated by Ramaswamy H. Sarma.
Keyphrases
- molecular dynamics
- binding protein
- induced apoptosis
- escherichia coli
- circulating tumor
- single molecule
- cell cycle arrest
- cell free
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- stem cells
- density functional theory
- transcription factor
- radiation therapy
- cell proliferation
- cell death
- pseudomonas aeruginosa
- quantum dots
- cystic fibrosis
- biofilm formation
- staphylococcus aureus
- virtual reality
- molecular dynamics simulations