Molecular dynamics simulation of shear- and stretch-induced dissociation of P-selectin/PSGL-1 complex
文献类型:期刊论文
作者 | Kang YY(康英永)![]() ![]() ![]() |
刊名 | BIOPHYSICAL JOURNAL
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出版日期 | 2012-01-04 |
卷号 | 102期号:1页码:112-120 |
通讯作者邮箱 | huobo@imech.ac.cn;mlong@imech.ac.cn |
关键词 | Selectin Glycoprotein Ligand-1 Granule Membrane-Protein P-Selectin Cell-Adhesion Beta-Switch Endothelial-Cells Catch Bonds Ib-Alpha Flow Transition |
ISSN号 | 0006-3495 |
产权排序 | [Kang, Yingyong;Lv, Shouqin;Ren, Peng;Huo, Bo;Long, Mian] Chinese Acad Sci, Inst Mech, Key Lab Micrograv, Natl Micrograv Lab, Beijing 100080, Peoples R China;[Kang, Yingyong;Lv, Shouqin;Ren, Peng;Huo, Bo;Long, Mian]Chinese Acad Sci, Inst Mech, Ctr Biomech & Bioengn, Beijing 100080, Peoples R China |
通讯作者 | Huo, B (reprint author), Chinese Acad Sci, Inst Mech, Key Lab Micrograv, Natl Micrograv Lab, Beijing 100080, Peoples R China. |
中文摘要 | By mediating the tethering and rolling of leukocytes on vascular surfaces, the interactions between P-selectin and the P-selectin glycoprotein ligand 1 (PSGL-1) play crucial roles during inflammation cascade. Tensile stretch produced by rolling leukocytes and shear stress exerted by blood flow constitute the two types of mechanical forces that act on the P-selectin/PSGL-1 bond. These forces modulate not only dissociation kinetics of this bond, but also the leukocyte adhesion dynamics. However, the respective contribution of the two forces to bond dissociation and to the corresponding microstructural bases remains unclear. To mimic the mechanical microenvironment, we developed two molecular dynamics approaches;namely, an approach involving the shear flow field with a controlled velocity gradient, and the track dragging approach with a defined trajectory. With each approach or with both combined, we investigate the microstructural evolution and dissociation kinetics of the P-LE/SGP-3 construct, which is the smallest functional unit of the P-selectin/PSGL-1 complex. The results demonstrate that both shear flow and tensile stretch play important roles in the collapse of the construct and that, before bond dissociation, the former causes more destruction of domains within the construct than the latter. Dissociation of the P-LE/SGP-3 construct features intramolecular destruction of the epidermal-growth-factor (EGF) domain and the breaking of hydrogen-bond clusters at the P-selectin-lectin/EGF interface. Thus, to better understand how mechanics impacts the dissociation kinetics of the P-selectin/PSGL-1 complex, we propose herein two approaches to mimic its physiological mechanical environment. |
学科主题 | 生物力学 |
分类号 | 一类 |
收录类别 | SCI |
资助信息 | This work was supported by the National Natural Science Foundation of China (30970707, 10702075, and 30730032), the National High-Technology Research and Development Program of China 2009AA02Z407), the National Key Basic Research Foundation of China (2011CB710904), and the Knowledge Innovation Project of the Chinese Academy of Sciences (KJCX2-YW-L08). |
原文出处 | http://dx.doi.org/10.1016/j.bpj.2011.11.4002 |
语种 | 英语 |
WOS记录号 | WOS:000298825400014 |
公开日期 | 2013-01-18 |
源URL | [http://dspace.imech.ac.cn/handle/311007/46556] ![]() |
专题 | 力学研究所_国家微重力实验室 |
推荐引用方式 GB/T 7714 | Kang YY,Lv SQ,Ren P,et al. Molecular dynamics simulation of shear- and stretch-induced dissociation of P-selectin/PSGL-1 complex[J]. BIOPHYSICAL JOURNAL,2012,102(1):112-120. |
APA | Kang YY,Lv SQ,Ren P,Huo B,&Long M.(2012).Molecular dynamics simulation of shear- and stretch-induced dissociation of P-selectin/PSGL-1 complex.BIOPHYSICAL JOURNAL,102(1),112-120. |
MLA | Kang YY,et al."Molecular dynamics simulation of shear- and stretch-induced dissociation of P-selectin/PSGL-1 complex".BIOPHYSICAL JOURNAL 102.1(2012):112-120. |
入库方式: OAI收割
来源:力学研究所
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