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. Author manuscript; available in PMC: 2014 Apr 1.
Published in final edited form as: Exp Eye Res. 2013 Feb 11;109:51–59. doi: 10.1016/j.exer.2013.01.016

Table 3.

Comparison of the rate of hydrolysis of MCA-62-70 substrate in different age groups of human and young bovine lens extracts.

Type of lens Cortex Nucleus

Specific activity (nmoles/mg protein/h) Total activity in cortex (nmoles/h) Specific activity (nmoles/h) protein/h) Total activity in nucleus (nmoles/mg
Human young (20 years) 0.28 ± 0.04** 7.86 ± 0.89 0.043 ± 0.003** 0.98 ± 0.07
Human middle aged (40 years) 0.37 ± 0.04*** 6.50 ± 0.78 0.032 ± 0.001*** 0.76 ± 0.05
Human old aged (60 years) 0.29 ± 0.02** 4.92 ± 0.27 0.037 ± 0.001** 0.57 ± 0.02
Bovine young 0.68 ± 0.07*** 95.87 ± 3.26 0.035 ± 0.001*** 7.53 ± 0.31

Water-soluble cortical and nuclear extracts (1 mg protein) of young, middle-aged and old human lenses were incubated with MCA-62-70 substrate (25 μg) at 37 °C for 2 h. Difference in fluorescence intensity was measured before and after incubation in a spectrofluorometer after excitation at 326 nm and emission at 398 nm. The amount of MCA-62-70 hydrolyzed was calculated by extrapolation of standard graph prepared by tryptic digestion of different concentrations of MCA-62-70 substrate. The values presented are average ± SE of four independent experiments. The data was analyzed by one-way ANOVA followed by Tukey’s multiple comparison test where **p<0.001 and ***p<0.0001, compared within lens groups of cortex and nucleus. Differences between lens groups of different ages were not significant.