研究论文

磷脂酰胆碱SUV 的NMR 研究

  • 李楠1 ,
  • 2 ,
  • 孙鹏1 ,
  • 2 ,
  • 刘买利1 ,
  • 张许1*
展开
  • 1. 波谱与原子分子物理国家重点实验室,武汉磁共振中心(中国科学院武汉物理与数学研究所),湖北 武汉,430071;
    2. 中国科学院大学,北京 100049
李楠(1987-),女,山西运城人,硕士研究生,从事液体核磁共振研究,无线电物理专业. *通讯联系人:张许,电话:027-87197056,E-mail:zhangxu@wipm.ac.cn.

收稿日期: 2014-04-24

  修回日期: 2014-10-28

  网络出版日期: 2014-12-05

基金资助

国家自然科学基金资助项目(21075132),国家重点基础研究发展计划(“973 计划”)资助项目(2013CB910200).

An NMR Study of Phosphatidylcholine Small Unilamellar Vesicles

  • LI Nan1 ,
  • 2 ,
  • SUN Peng1 ,
  • 2 ,
  • LIU Mai-li1 ,
  • ZHANG Xu1*
Expand
  • 1. State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Center for Magnetic Resonance (Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences), Wuhan 430071, China;
    2. University of Chinese Academy Sciences, Beijing 100049, China
*Corresponding author:ZHANG Xu: Tel: 027-87197056,E-mail: zhangxu@wipm.ac.cn.

Received date: 2014-04-24

  Revised date: 2014-10-28

  Online published: 2014-12-05

Supported by

国家自然科学基金资助项目(21075132),国家重点基础研究发展计划(“973 计划”)资助项目(2013CB910200).

摘要

磷脂酰胆碱(PC)是人和动物血液中大量存在的一类具有重要生物功能的磷脂,它和鞘磷脂一起形成了不同大小的密度脂蛋白,对血液中胆固醇等分子的转运和代谢起着至关重要的作用.脂蛋白中磷脂的组成和形态变化与某些疾病,如动脉粥样硬化、癌症和老年痴呆等的发生和发展密切相关,因此研究磷脂的组成形态将有助于明确磷脂的生物化学作用.该文采用一维(1D)和二维(2D) NMR 技术对PC 所形成的SUV (small unilamellar vesicle)结构进行了分析,通过对PC 磷脂头部氮甲基的检测分析,发现PC 所形成的SUV为较为稳定的双层结构,这表明通常的磷脂脂蛋白可能是一种双层膜结构,而非通常所认为的单层结构.

本文引用格式

李楠1 , 2 , 孙鹏1 , 2 , 刘买利1 , 张许1* . 磷脂酰胆碱SUV 的NMR 研究[J]. 波谱学杂志, 2014 , 31(4) : 572 -578 . DOI: 10.11938/cjmr20140411

Abstract

Phosphatidylcholines (PC) is one of the most important phospholipids in the human and animal serum. It is the major constituent of lipoproteins that play important roles in the transport and metabolism of cholesterol. It was found that the many diseases, such as atherosclerosis, cancer, dementia and so on, were often associated with compositional and structural changes of phospholipids. Therefore, it is of interest to study the composition and structure of phospholipids. Here, small unilamellar vesicles (SUV) formed by PC were studied using 1D and 2D NMR experiments. It was found that there were two different [-N+(CH3)3] signals of PC, indicating that the SUV formed by PC may have a bilayer-spherical structure, not as previously thought to be a mono-layer structure.

参考文献

[1] Filippov A, Munavirov B, Grobner G, et al. Lateral diffusion in equimolar mixtures of natural sphingomyelins with dioleoylphosphatidylcholine[J]. Magn Reson Imaging, 2012, 30(3): 413―421.

[2] Smaby J M, Brockman H L, Brown R E. Cholesterol's interfacial interactions with sphingomyelins and phosphatidylcholines: hydrocarbon chain structure determines the magnitude of condensation[J]. Biochemistry, 1994, 33(31): 9 135―9 142.

[3] Slotte J P. Sphingomyelin-cholesterol interactions in biological and model membranes[J]. Chem Phys Lipids, 1999, 102(1-2): 13―27.

[4] Ramstedt B, Slotte J P. Interaction of cholesterol with sphingomyelins and acyl-chain-matched phosphatidylcholines: a comparative study of the effect of the chain length[J]. Biophys J, 1999, 76(2): 908―915.

[5] Brown D A, London E. Structure and function of sphingolipid- and cholesterol-rich membrane rafts[J]. J Biol Chem, 2000, 275(23): 17 221―17 224.

[6] Edidin M. The state of lipid rafts: from model membranes to cells[J]. Annu Rev Biophys Biomol Struct, 2003, 32: 257―283.

[7] Mayor S, Rao M. Rafts: Scale-dependent, active lipid organization at the cell surface[J]. Traffic, 2004, 5(4): 231―240.

[8] Pike L J. Lipid rafts: heterogeneity on the high seas[J]. Biochem J, 2004, 378: 281―292.

[9] Simons K, Ikonen E. Functional rafts in cell membranes[J]. Nature, 1997, 387(6633): 569―572.

[10] Niemela P, Hyvonen M T, Vattulainen I. Structure and dynamics of sphingomyelin bilayer: Insight gained through systematic comparison to phosphatidylcholine[J]. Biophys J, 2004, 87(5): 2 976―2 989.

[11] Niemela P S, Hyvonen M T, Vattulainen I. Influence of chain length and unsaturation on sphingomyelin bilayers[J]. Biophys J, 2006, 90(3): 851―863.

[12] Barenholz Y, Thompson T E. Sphingomyelin: biophysical aspects[J]. Chem Phys Lipids, 1999, 102(1-2): 29―34.

[13] Murphy H C, AlaKorpela M, White J J, et al. Evidence for distinct behaviour of phosphatidylcholine and sphingomyelin at the low density lipoprotein surface[J]. Biochem Bioph Res Co, 1997, 234(3): 733―737.

[14] Bi Yun-chen(毕允晨), Wang Yu-juan(王玉娟), Wang Jun-feng(王俊峰). The nanodics: A novel tool to study membrane protein structure and function(Nanodisc 体系在膜蛋白结构与功能研究中的应用)[J]. Chinese J Magn Reson(波谱学杂志), 2011, 28(2): 177―189.

[15] Campos H, Genest J J Jr., Blijlevens E, et al. Low density lipoprotein particle size and coronary artery disease[J]. Arterioscler Thromb, 1992, 12(2): 187―195.

[16] Havel R J. Citation classic - the distribution and chemical-composition of ultracentrifugally separated lipoproteins in human-serum[J]. Cc/Life Sci, 1983(46): 23―23.

[17] Tall A R. Plasma high density lipoproteins. Metabolism and relationship to atherogenesis[J]. J Clin Invest, 1990, 86(2): 379―384.

[18] Reichl D, Miller N E. The anatomy and physiology of reverse cholesterol transport[J]. Clin Sci, 1986, 70(3): 221―231.

[19] Gordon D J, Rifkind B M. High-density lipoprotein - the clinical implications of recent studies[J]. New Engl J Med, 1989, 321(19): 1 311―1 316.

[20] Miller N E. HDL metabolism and its role in lipid transport[J]. Eur Heart J, 1990, 11: 1―3.


[21] Johnson W J, Mahlberg F H, Rothblat G H, et al. Cholesterol transport between cells and high-density-lipoproteins[J]. Biochimica et biophysica Acta, 1991, 1 085(3): 273―298.

[22] Huang Y D, Voneckardstein A, Assmann G. Cell-derived unesterified cholesterol cycles between different HDLs and LDL for its effective esterification in plasma[J]. Arterioscler Thromb, 1993, 13(3): 445―458.

[23] Fajardo V A, McMeekin L, LeBlanc P J. Influence of phospholipid species on membrane fluidity: a meta-analysis for a novel phospholipid fluidity index[J]. J Membr Biol, 2011, 244(2): 97―103.

[24] Schneider P B. Permanent sensitive stain for choline-containing phospholipids on thin-layer chromatograms[J]. J Lipid Res, 1966, 7(1): 169―170.

[25] Jungalwala F B, Evans J E, McCluer R H. High-performance liquid chromatography of phosphatidylcholine and sphingomyelin with detection in the region of 200 nm[J]. Biochem J, 1976, 155(1): 55―60.

[26] Mallol R, Rodriguez M A, Brezmes J, et al. Human serum/plasma lipoprotein analysis by NMR: application to the study of diabetic dyslipidemia[J]. Prog Nucl Magn Reson Spectr, 2013, 70: 1―24.

[27] Mao J, Jiang L, Jiang B, et al. 1H-14N HSQC detection of choline-containing compounds in solutions[J]. J Magn Reson, 2010, 206(1): 157―160.

[28] Mao Xi-an(毛希安). A simple method for clean water signal suppression(一个获得压水峰良好效果的简单方法)[J]. Chinese J Magn Reson(波谱学杂志), 2014, 31(1): 1―6

[29] Schmidt C F, Barenholz Y, Thompson T E. A nuclear magnetic resonance study of sphingomyelin in bilayer systems[J]. Biochemistry, 1977, 16(12): 2 649―2 656.

文章导航

/