Achievements and perspectives of top-down proteomics

被引:57
|
作者
Armirotti, Andrea [1 ]
Damonte, Gianluca [2 ,3 ]
机构
[1] Adv Biotechnol Ctr, I-16132 Genoa, Italy
[2] Univ Genoa, Dept Expt Med, Genoa, Italy
[3] Ctr Excellence Biomed Res, Genoa, Italy
关键词
ESI; LC-MS; MALDI; Phosphorylation; Technology; Top-down; ELECTRON-CAPTURE DISSOCIATION; TANDEM MASS-SPECTROMETRY; COLLISIONALLY ACTIVATED DISSOCIATION; PROTEIN IDENTIFICATION TECHNOLOGY; CHROMATOGRAPHIC TIME-SCALE; MULTIPLY-CHARGED IONS; IN-SOURCE DECAY; INTACT PROTEINS; BOTTOM-UP; REVERSED-PHASE;
D O I
10.1002/pmic.201000245
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Over the last years, top-down (TD) MS has gained a remarkable space in proteomics, rapidly trespassing the limit between a promising approach and a solid, established technique. Several research groups worldwide have implemented TD analysis in their routine work on proteomics, deriving structural information on proteins with the level of accuracy that is impossible to achieve with classical bottom-up approaches. Complete maps of PTMs and assessment of single aminoacid polymorphisms are only a few of the results that can be obtained with this technique. Despite some existing technical and economical limitations, TD analysis is at present the most powerful instrument for MS-based proteomics and its implementation in routine workflow is a rapidly approaching turning point in proteomics. In this review article, the state-of-the-art of TD approach is described along with its major advantages and drawbacks and the most recent trends in TD analysis are discussed. References for all the covered topics are reported in the text, with the aim to support both newcomers and mass spectrometrists already introduced to TD proteomics.
引用
收藏
页码:3566 / 3576
页数:11
相关论文
共 50 条
  • [1] Top-down proteomics
    Roberts, David S.
    Loo, Joseph A.
    Tsybin, Yury O.
    Liu, Xiaowen
    Wu, Si
    Chamot-Rooke, Julia
    Agar, Jeffrey N.
    Pasa-Tolic, Ljiljana
    Smith, Lloyd M.
    Ge, Ying
    [J]. NATURE REVIEWS METHODS PRIMERS, 2024, 4 (01):
  • [2] Top-down proteomics
    不详
    [J]. NATURE REVIEWS METHODS PRIMERS, 2024, 4 (01):
  • [3] Top-down proteomics
    Kelleher, NL
    [J]. ANALYTICAL CHEMISTRY, 2004, 76 (11) : 196A - 203A
  • [4] Advancements in Top-Down Proteomics
    Zhou, Hu
    Ning, Zhibing
    Starr, Amanda E.
    Abu-Farha, Mohamed
    Figeys, Daniel
    [J]. ANALYTICAL CHEMISTRY, 2012, 84 (02) : 720 - 734
  • [5] Tearing the Top Off 'Top-Down' Proteomics
    Perkel, Jeffrey M.
    [J]. BIOTECHNIQUES, 2012, 53 (02) : 75 - +
  • [6] Top-down proteomics for the analysis of proteolytic events - Methods, applications and perspectives
    Tholey, Andreas
    Becker, Alexander
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2017, 1864 (11): : 2191 - 2199
  • [7] Editorial: Breakthroughs in top-down proteomics
    Penque, Deborah
    Marcus, Katrin
    Torres, Vukosaca Milic
    [J]. JOURNAL OF PROTEOMICS, 2018, 175 : 1 - 2
  • [8] An FDR metric for top-down proteomics
    Doerr, Allison
    [J]. NATURE METHODS, 2019, 16 (03) : 218 - 218
  • [9] Special Focus on Top-down Proteomics
    Huber, Christian
    Huber, Lukas
    [J]. PROTEOMICS, 2010, 10 (20) : 3564 - 3565
  • [10] A photocleavable surfactant for top-down proteomics
    Kyle A. Brown
    Bifan Chen
    Tania M. Guardado-Alvarez
    Ziqing Lin
    Leekyoung Hwang
    Serife Ayaz-Guner
    Song Jin
    Ying Ge
    [J]. Nature Methods, 2019, 16 : 417 - 420