Fenyo David, Wang Qingjun, DeGrasse Jeffrey A, Padovan Julio C, Cadene Martine, Chait Brian T
Laboratory of Mass Spectrometry and Gaseous Ion Chemistry, Rockefeller University, USA.
J Vis Exp. 2007(3):192. doi: 10.3791/192. Epub 2007 Apr 29.
This video demonstrates the preparation of an ultra-thin matrix/analyte layer for analyzing peptides and proteins by Matrix-Assisted Laser Desorption Ionization Mass Spectrometry (MALDI-MS) (1, 2). The ultra-thin layer method involves the production of a substrate layer of matrix crystals (alpha-cyano-4-hydroxycinnamic acid) on the sample plate, which serves as a seeding ground for subsequent crystallization of a matrix/analyte mixture. Advantages of the ultra-thin layer method over other sample deposition approaches (e.g. dried droplet) are that it provides (i) greater tolerance to impurities such as salts and detergents, (ii) better resolution, and (iii) higher spatial uniformity. This method is especially useful for the accurate mass determination of proteins. The protocol was initially developed and optimized for the analysis of membrane proteins and used to successfully analyze ion channels, metabolite transporters, and receptors, containing between 2 and 12 transmembrane domains (2). Since the original publication, it has also shown to be equally useful for the analysis of soluble proteins. Indeed, we have used it for a large number of proteins having a wide range of properties, including those with molecular masses as high as 380 kDa (3). It is currently our method of choice for the molecular mass analysis of all proteins. The described procedure consistently produces high-quality spectra, and it is sensitive, robust, and easy to implement.
本视频展示了用于通过基质辅助激光解吸电离质谱法(MALDI-MS)分析肽和蛋白质的超薄基质/分析物层的制备方法(1,2)。超薄层方法包括在样品板上制备基质晶体(α-氰基-4-羟基肉桂酸)的底物层,该层作为基质/分析物混合物后续结晶的晶种层。与其他样品沉积方法(如干滴法)相比,超薄层方法的优点在于它(i)对盐和去污剂等杂质具有更高的耐受性,(ii)具有更好的分辨率,以及(iii)具有更高的空间均匀性。该方法对于蛋白质的精确质量测定特别有用。该方案最初是为分析膜蛋白而开发和优化的,并用于成功分析含有2至12个跨膜结构域的离子通道、代谢物转运体和受体(2)。自最初发表以来,它已被证明对可溶性蛋白质的分析同样有用。实际上,我们已将其用于大量具有广泛特性的蛋白质,包括分子量高达380 kDa的蛋白质(3)。它目前是我们用于所有蛋白质分子量分析的首选方法。所描述的程序始终能产生高质量的光谱,并且它灵敏、稳健且易于实施。