Mass spectrometry of native rat amelogenins: Primary transcripts, secretory isoforms, and C-terminal degradation

Cloning technologies have established unambiguously that amelogenins always seem larger in molecular weight (M-r) by gel electrophoresis (SDS-PAGE) than by mass spectrometry (MS). This has caused many problems relating cloned versions of amelogenin to proteins actually secreted by ameloblasts in vivo. In this study, discrete protein fractions at 31-20 kDa (M-r(SDS)) were prepared 60m freeze-dried rat incisor enamel by techniques optimized for preserving protein integrity. N-terminal sequence and amino acid compositional analyses indicated that the major protein forming these fractions was amelogenin. As expected, the molecular weights estimated by matrix-assisted laser desorption ionization (MALDI) and electrospray ionization (ESI) MS were significantly less than their apparent molecular weights estimated by SDS-PACE. Plots of M-r(SDS) vs. M-r(MS) for all fractions showed high linear correlation (r = 0.992). Analysis of MS data further indicated that the major protein in the 27-kDa fraction corresponded to the R180 secretory isoform of rat amelogenin, whereas some minor proteins in the 23-kDa fraction likely corresponded to a R156 secretory isoform. This was in contrast to major proteins forming the 25-, 24-, and 23-kDa fractions (M-r(SDS)), which seemed to represent proteolytic fragments of R180 progressively altered at the P-169-A(170), P-164-L-165, and F-151-S-152 C-terminal cleavage sites, respectively. Proteins in the 20-kDa fraction (M-r(SDS)) most closely matched by ESI-MS fragments of the R156 secretory isoform that were C-terminally-modified at the equivalent P-164-L-165 site.