Why the Orientational Mobility in Arginine and Lysine Spacers of Peptide Dendrimers Designed for Gene Delivery Is Different?

被引:6
|
作者
Bezrodnyi, Valeriy V. [1 ,2 ,3 ]
Shavykin, Oleg V. [1 ,2 ,3 ]
Mikhtaniuk, Sofia E. [2 ,3 ]
Neelov, Igor M. [2 ,3 ]
Sheveleva, Nadezhda N. [1 ]
Markelov, Denis A. [1 ]
机构
[1] St Petersburg State Univ, 7-9 Univ Skaya Nab, St Petersburg 199034, Russia
[2] ITMO Univ, St Petersburg Natl Res Univ Informat Technol Mech, Fac Appl Opt, Kronverkskiy Pr 49, St Petersburg 197101, Russia
[3] ITMO Univ, St Petersburg Natl Res Univ Informat Technol Mech, Bioengn Inst, Kronverkskiy Pr 49, St Petersburg 197101, Russia
基金
俄罗斯科学基金会;
关键词
peptide dendrimer; computer simulation; molecular dynamics; zeta potential; NMR; spin-lattice relaxation time; MOLECULAR-DYNAMICS SIMULATION; LATTICE NMR RELAXATION; POLY-L-LYSINE; BROWNIAN DYNAMICS; HYPERBRANCHED POLYMERS; PAMAM DENDRIMERS; LOCAL DYNAMICS; SIRNA; CHAIN; FIELD;
D O I
10.3390/ijms21249749
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
New peptide dendrimer with Lys-2Arg repeating units was recently studied experimentally by NMR (RSC Advances, 2019, 9, 18018) and tested as gene carrier successfully (Int. J. Mol. Sci., 2020, 21, 3138). The unusual slowing down of the orientational mobility of 2Arg spacers in this dendrimer was revealed. It has been suggested that this unexpected behavior is caused by the Arg-Arg pairing effect in water, which leads to entanglements between dendrimer branches. In this paper, we determine the reason for this slowing down using atomistic molecular dynamics simulation of this dendrimer. We present that the structural properties of Lys-2Arg dendrimer are close to those of the Lys-2Lys dendrimer at all temperatures (Polymers, 2020, 12, 1657). However, the orientational mobility of the H-H vector in CH2-N groups of 2Arg spacers in Lys-2Arg dendrimer is significantly slower than the mobility of the same vector in the Lys-2Lys dendrimer. This result is in agreement with the recent NMR experiments for the same systems. We revealed that this difference is not due to the arginine-arginine pairing, but is due to the semiflexibility effect associated with the different contour length from CH2-N group to the end of the side arginine or lysine segment in spacers.
引用
收藏
页码:1 / 22
页数:22
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