Ion mobility-mass spectrometry and orthogonal gas-phase techniques to study amyloid formation and inhibition

被引:37
|
作者
Hoffmann, Waldemar [1 ,2 ]
von Helden, Gert [2 ]
Pagel, Kevin [1 ,2 ]
机构
[1] Free Univ Berlin, Inst Chem & Biochem, Takustr 3, D-14195 Berlin, Germany
[2] Max Planck Gesell, Fritz Haber Inst, Faradayweg 4-6, D-14195 Berlin, Germany
关键词
ALZHEIMERS-DISEASE; FIBRIL FORMATION; INFRARED-SPECTROSCOPY; PROTEIN AGGREGATION; MOLECULAR TWEEZERS; BETA; PEPTIDE; OLIGOMERS; A-BETA-42; INSIGHTS;
D O I
10.1016/j.sbi.2017.03.002
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
Amyloidogenic peptide oligomers are responsible for a variety of neurodegenerative disorders such as Alzheimer's and Parkinson's disease. Due to their dynamic, polydisperse, and polymorphic nature, these oligomers are very challenging to characterize using traditional condensed-phase methods. In the last decade, ion mobility-mass spectrometry (IM-MS) and related gas-phase techniques have emerged as a powerful alternative to disentangle the structure and assembly characteristics of amyloid forming systems. This review highlights recent advances in which IM-MS was used to characterize amyloid oligomers and their underlying assembly pathway. In addition, we summarize recent studies in which IM-MS was used to size- and mass-select species for a further spectroscopic investigation and outline the potential of IM-MS as a tool for the screening of amyloid inhibitors.
引用
收藏
页码:7 / 15
页数:9
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