Mechanical, structural, and dynamical modifications of cholesterol exposed porcine aortic elastin

被引:6
作者
Bilici, Kubra [1 ]
Morgan, Steven W. [2 ]
Silverstein, Moshe C. [1 ]
Wang, Yunjie [3 ]
Sun, Hyung Jin [3 ]
Zhang, Yanhang [3 ,4 ]
Boutis, Gregory S. [1 ,5 ]
机构
[1] CUNY Brooklyn Coll, Dept Phys, 2900 Bedford Ave, Brooklyn, NY 11210 USA
[2] Univ Minnesota, Div Sci & Math, 600 E 4th St Moris, Moris, MN USA
[3] Boston Univ, Dept Mech Engn, 110 Cummington Mall, Boston, MA 02215 USA
[4] Boston Univ, Dept Biomed Engn, 110 Cummington Mall, Boston, MA 02215 USA
[5] CUNY, Grad Ctr, Dept Phys, 365 5th Ave, New York, NY USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Elastin; C-13 MAS NMR; H-2; NMR; Cholesterol; ARTERIAL STIFFNESS; LIPID-ACCUMULATION; BIOLOGICAL ROLES; NMR; C-13; PROTEIN; WATER; TEMPERATURE; MOBILITY; H-1;
D O I
10.1016/j.bpc.2016.09.002
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
Elastin is a protein of the extracellular matrix that contributes significantly to the elasticity of connective tissues. In this study, we examine dynamical and structural modifications of aortic elastin exposed to cholesterol by NMR spectroscopic and relaxation methodologies. Macroscopic measurements are also presented and reveal that cholesterol treatment May cause a decrease in the stiffness of tissue. H-2 NMR relaxation techniques revealed differences between the relative populations of water that correlate with the swelling of the tissue following cholesterol exposure. C-13 magic-angle-spinning NMR spectroscopy and relaxation methods indicate that cholesterol treated aortic elastin is more mobile than control samples. Molecular dynamics simulations on a short elastin repeat VPGVG in the presence of cholesterol are used to investigate the energetic and entropic contributions to the retractive force, in comparison to the same peptide in water. Peptide stiffness is observed to reduce following cholesterol exposure due to a decrease in the entropic force. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 57
页数:11
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