Analysis of water-soluble crystallins from human lenses, ages 32 week fetal to 55 years has led to identification of the major modifications of the proteins comprising the lens. These modifications were identified by the masses of the proteins determined by electrospray ionization mass spectrometry after the proteins were separated by gel filtration and reversed phase high performance liquid chromatography. Examination of all the proteins isolated from the water soluble portion demonstrated that the major agerelated modifications causing significant alteration in the molecular weights of the lens crystallins include truncation of the N-termini of βB1, βA3 and βA1, and partial phosphorylation and C-terminal degradation of α- crystallins. N-terminal degradation of βB1, βA3 and βA1 was evident in human lenses less than one year old, and the proportion of these truncated proteins became greater with age. Phosphorylation of αA- and αB-crystallins increased from the fetal to the 3 year old lens, but did not change with further aging. Minor components indicating truncation of the C-termini of α- crystallins were found in older lenses. In contrast to βB1, βA3 and βA1, the masses of the major species of αA, αB, βB2. βA4, γS, γC, and γD did not change with aging. This suggested that the major modifications to these crystallins are limited to deamidation and possibly intra-molecular disulfide bonds. These data in conjunction with the data in the accompanying manuscript, established deamidation as a common modification, since deamidation, which causes only a one dalton change in mass, is the only modification that is consistent with the absence of a detectable change in molecular weight and the observed increased acidity demonstrated in the two- dimensional gels of the accompanying paper. Other age related changes included a decrease in βB3 (M(r) 2424), a major component of the fetal lens, which was not detected m lenses older than 3 years, and increases in the ratios of αB:αA and γS:γC.
- Mass spectrometry
- Modifications of lens crystallins
ASJC Scopus subject areas
- Sensory Systems
- Cellular and Molecular Neuroscience