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蛋白质组学技术用于晶状体蛋白的研究进展 被引量:2

he progress of proteomics approaches in cataract research
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摘要 近年来,晶状体蛋白质组学的相关研究日渐广泛。蛋白质组学技术以其高通量、高效率等优势,为晶状体这一人体内蛋白质含量最高组织的蛋白质组学研究提供了可靠的技术支撑,从而为揭示年龄相关性白内障的发生机制提供了新思路和新方向。本文就蛋白质组学的分离、鉴定及相关新技术在晶状体蛋白研究中的应用进展做一系统综述。(中华腠科杂岙,2012,48:952—955) Researches on lens proteomics are becoming prevalent in recent years. Characterized by their high resolusion and efficiency, proteomics approaches provide reliable methodological support for lenses proteomic research, which demonstrates a new orientation for revealing the mechanism of cataractogenesis. This review outlines the separation, identification and some novel approaches of proteomic techniques applied in recent lenses proteomie research. (Chin J Ophthalmol , 2012,48:952-955 )
出处 《中华眼科杂志》 CAS CSCD 北大核心 2012年第10期952-955,共4页 Chinese Journal of Ophthalmology
关键词 晶状体蛋白 白内障 蛋白质组学技术 Crystallin Cataract Proteomies,methods
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  • 1Bloemendal H. Vertebrate Eye Lens. Science, 1977 ,197 : 127-138.
  • 2Takemoto L,Boyle D. Increased deamidation of asparagine duringhuman senile cataractogenesis. Mol Vis ,2000,6 : 164-168.
  • 3Wilmarth PA, Tanner S, Dasari S, et al. Age-related changes inhuman crystallins determined from comparative analysis of post-translational modifications in young and aged lens: doesdeamidation contribute to crystallin insolubility? J Proteome Res,2006,5:2554-2566.
  • 4Zhang CW, Liu P, Wang NL, et al. Comparison of two tandemmass spectrometry-based methods for analyzing the proteome ofhealthy human lens fibers. Mol Vis ,2007 ,13 : 1873-1877.
  • 5Grey AC,Schey KL. Distribution of bovine and rabbit lens alpha-crystallin products by MALDI imaging mass spectrometry. MolVis,2008,14:171-179.
  • 6吕济相,王济明,罗诗樵,黄国飞.差异蛋白质组学样品的制备[J].中华内分泌外科杂志,2010,4(2):135-137. 被引量:4
  • 7Wang Z,Han J,Schey KL. Spatial differences in an integralmembrane proteome detected in laser capture microdissectedsamples. J Proteome Res,2008 ,7 :2696-2702.
  • 8Asomugha CO, Gupta R, Srivastava OP. Identification ofcrystallin modifications in the human lens cortex and nucleus usinglaser capture microdissection and CyDye labeling. Mol Vis,2010,16:476494.
  • 9Miao A, Dai Y, Ji Y, et al. Liquid-chromatographic and mass-spectrometric identification of lens proteins using microwave-assisted digestion with trypsin-immobilized magnetic nanoparticles.Biochem Biophys Res Commun, 2009 ,380 : 603 -608.
  • 10Kibbelaar M, Bloemendal H. The topography of lens proteinsbased on chromatography and two-dimensional gel electrophoresis.Exp Eye Res,1975 ,21:25-36.

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  • 1祁磊,林媛.年龄相关性白内障的防治进展[J].海峡科学,2010(5):51-53. 被引量:3
  • 2魏湘铭,魏冠男.复明片治疗未成熟期老年性白内障临床观察[J].国际眼科杂志,2007,7(1):277-279. 被引量:4
  • 3葛坚.眼科学[M].第2版.北京:人民卫生出版社,2013:185-186.
  • 4Asornuqha CO, Gupta R, Srivastava OP, Identification of crystallin modifications in the human lens cortex and nucleus laser using laser capture microdissection and CyDye labeling[J]. Mol Vis, 2010, 16: 476-494.
  • 5MacCoss MJ,McDonald WH,Saraf A,et al. Shotgun identification of protein modifications from protein complexes and lens tissue[J]. Proc Natl Acad Sci U S A, 2002, 99(12): 7900-7905.
  • 6Schaefer H,Marcus K,Sickmann A,et al. Identification of phosphorylation and acetylation sites in alphaA-crystallin of the eye lens(mus rnusculus)after two-dimensional gel electrophoresis[J]. Anal Bioanal Chern,2003,376(7):966-972.
  • 7Ueda Y,Duncan MK,David LL. Lens proteomics: the accumulation of crystallin modifications in the mouse lens with age[J]. Invest Ophthalmol Vis Sei,2002,43(1 ):205-215.
  • 8Kamei A,Takarnura S,Nagai M,et al. Phosphoproteome analysis of hereditary cataractous rat lens alpha-crystallin[J]. Biol Pharm Bull,2004,27(12):1923-1931.
  • 9Grey AC,Schey KL. Distribution of bovine and rabbit lens alpha-crystallin products by MALDI imaging mass spectrometry[J]. Mol Vis,2008,14:171-179.
  • 10Kyselova Z. Mass spectrometry-based proteomies approaches applied in cataract research[J]. Mass Spectrom Rev,201|, 30(6):1173-1184.

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