McLafferty F W, Kelleher N L, Begley T P, Fridriksson E K, Zubarev R A, Horn D M
Baker Chemistry Laboratory, Cornell University, Ithaca, NY 14853-1301, USA.
Curr Opin Chem Biol. 1998 Oct;2(5):571-8. doi: 10.1016/s1367-5931(98)80085-9.
Multiple dimensions of unique molecular structure information can now be obtained from proteins and DNA using mass spectrometry. Less than 10(-16) mol of the active major histocompatibility complex signaling peptide in a mixture of thousands can be identified. For large proteins (> 40 kDa), the high resolving power (> 10(5) and 10(-17) mol sensitivity of Fourier-transform mass spectrometry provide exact molecular weight values (+/- 1 or 2 Da) for mixture components, indicating error or modifications compared with the predicted DNA sequence. Selecting a specific molecular species, its two-dimensional spectrum indicates the part of the molecule that is modified; a three-dimensional spectrum of that fragment further isolates the modification site.