TY - JOUR
T1 - Geometry-Based Self-Assembly of Histone–DNA Nanostructures at Single-Nucleotide Resolution
AU - Serag, Maged F.
AU - Aikeremu, Aimaiti
AU - Tsukamoto, Ryoko
AU - Piwonski, Hubert Marek
AU - Abadi, Maram
AU - Kaji, Noritada
AU - Dwyer, Jason R.
AU - Baba, Yoshinobu
AU - Habuchi, Satoshi
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: We thank Dr. R. Sougrat for the TEM and cryo-TEM images of histones and histone–DNA complexes. We thank Prof. E. Yashima for providing access to the dry-phase AFM facility in his lab. We thank Dr. M. Shuaib for the helpful discussions. Schematic illustrations in the figures were created by H. Hwang, scientific illustrator at King Abdullah University of Science and Technology. The research reported in this publication was supported by funding from King Abdullah University of Science and Technology (KAUST) and from Nagoya University.
PY - 2019/6/25
Y1 - 2019/6/25
N2 - Histones are basic protein monomers capable of interacting with DNA, providing the mechanism of DNA compaction inside the cell nucleus. The well-ordered assembly process of histone and DNA is a potential candidate as the approach for building DNA–protein nanostructures. Here, utilizing the sequence-independent histone–DNA interaction, we present an approach to self-assemble histones and single-stranded DNA (ssDNA) to form well-defined histone–DNA (sHD) nanoparticles and their multidimensional cross-linked complexes (cHD). By using various molecular biology and microscopy techniques, we elucidate the structure of these complexes, and we show that they are formed at carefully controlled conditions of temperature, ionic strength, concentration, and incubation time. We also demonstrate using a set of ssDNA molecular rulers and a geometric accommodation model that the assembly of sHD and cHD particles proceeds with precise geometry so that the number of ssDNA in these particles can be programmed by the length of ssDNA. We further show that the formation of cHD amplifies the effect of the length of ssDNA on the self-assembly, allowing for distinguishing ssDNA of different lengths at single nucleotide resolution. We envision that our geometry-directed approach of self-assembling histone–DNA nanostructures and the fundamental insights can serve as a structural platform to advance building precisely ordered DNA–protein nanostructures.
AB - Histones are basic protein monomers capable of interacting with DNA, providing the mechanism of DNA compaction inside the cell nucleus. The well-ordered assembly process of histone and DNA is a potential candidate as the approach for building DNA–protein nanostructures. Here, utilizing the sequence-independent histone–DNA interaction, we present an approach to self-assemble histones and single-stranded DNA (ssDNA) to form well-defined histone–DNA (sHD) nanoparticles and their multidimensional cross-linked complexes (cHD). By using various molecular biology and microscopy techniques, we elucidate the structure of these complexes, and we show that they are formed at carefully controlled conditions of temperature, ionic strength, concentration, and incubation time. We also demonstrate using a set of ssDNA molecular rulers and a geometric accommodation model that the assembly of sHD and cHD particles proceeds with precise geometry so that the number of ssDNA in these particles can be programmed by the length of ssDNA. We further show that the formation of cHD amplifies the effect of the length of ssDNA on the self-assembly, allowing for distinguishing ssDNA of different lengths at single nucleotide resolution. We envision that our geometry-directed approach of self-assembling histone–DNA nanostructures and the fundamental insights can serve as a structural platform to advance building precisely ordered DNA–protein nanostructures.
UR - http://hdl.handle.net/10754/656041
UR - http://pubs.acs.org/doi/10.1021/acsnano.9b03259
UR - http://www.scopus.com/inward/record.url?scp=85070485879&partnerID=8YFLogxK
U2 - 10.1021/acsnano.9b03259
DO - 10.1021/acsnano.9b03259
M3 - Article
C2 - 31244030
SN - 1936-0851
VL - 13
SP - 8155
EP - 8168
JO - ACS Nano
JF - ACS Nano
IS - 7
ER -