Miranker A D
Department of Molecular Biophysics and Biochemistry, Yale University, 260 Whitney Avenue, PO Box 208114, New Haven, CT 06520, USA.
Curr Opin Struct Biol. 2000 Oct;10(5):601-6. doi: 10.1016/s0959-440x(00)00137-8.
The utility of mass spectrometry for the analysis of proteins has grown enormously in the past decade. Significant advances in detection and ionization techniques are allowing questions about noncovalent assembly to be addressed by the direct observation of gas phase complexes, their assembly in real time and their disassembly by perturbation of solution or instrument conditions. These technological innovations have plainly captured the imagination of biological researchers. Recent and novel developments include the combination of mass spectrometry with isotopic labeling, affinity labeling and genomic information. Collectively, these advances are opening new doors to the isolation of complexes, the identification of their substituents and the characterization of their conformations and assembly.
在过去十年中,质谱分析蛋白质的实用性有了极大的提高。检测和电离技术的重大进展使得通过直接观察气相复合物、它们的实时组装以及通过改变溶液或仪器条件使其解离,来解决有关非共价组装的问题成为可能。这些技术创新显然激发了生物学研究人员的想象力。最近的新进展包括将质谱与同位素标记、亲和标记和基因组信息相结合。总体而言,这些进展为复合物的分离、其取代基的鉴定以及其构象和组装的表征打开了新的大门。