Regulation of chromatin architecture by protein binding: insights from molecular modeling

被引:2
作者
Portillo-Ledesma, Stephanie [1 ,4 ]
Schlick, Tamar [1 ,2 ,3 ,4 ]
机构
[1] NYU, Dept Chem, 100 Washington Sq East,Silver Bldg, New York, NY 10003 USA
[2] NYU, Courant Inst Math Sci, 251 Mercer St, New York, NY 10012 USA
[3] NYU, NYU Shanghai, East China Normal Univ, Ctr Computat Chem, Shanghai 200122, Peoples R China
[4] NYU, Simons Ctr Computat Phys Chem, 24 Waverly Pl,Silver Bldg, New York, NY 10003 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Histone and non-histone proteins; Molecular modeling; Nucleosome; Chromatin; Chromosome; HISTONE METHYLTRANSFERASE ACTIVITY; LINKER HISTONE; SOMATIC MUTATIONS; RECOGNIZING DNA; LYSINE; 9; NUCLEOSOME; DYNAMICS; RECOGNITION; COMPLEX; H3;
D O I
10.1007/s12551-024-01195-5
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Histone and non-histone proteins play key roles in the activation and repression of genes. In addition to experimental studies of their regulation of gene expression, molecular modeling at the nucleosome, chromatin, and chromosome levels can contribute insights into the molecular mechanisms involved. In this review, we provide an overview for protein-bound chromatin modeling, and describe how our group has integrated protein binding into genome systems across the scales, from all-atom to coarse-grained models, using explicit to implicit descriptions. We describe the associated applications to protein binding effects and biological mechanisms of genome folding and gene regulation. We end by illustrating the application of machine learning tools like AlphaFold2 to proteins relevant to chromatin systems.
引用
收藏
页码:331 / 343
页数:13
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