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Effect of age on acetylcholinesterase and other hemolymph proteins in Aplysia
Authors:Malathi Srivatsan  Bertram Peretz  Brent Hallahan  Ramesh Talwalker
Institution:(1) Department of Physiology and Biophysics, University of Kentucky Medical Center, 40536-0084 Lexington, KY, USA;(2) Department of Medicine, University of Kentucky Medical Center, 40536-0084 Lexington, KY, USA
Abstract:Summary Hemolymph was examined in young (ca. 86 days old), mature (ca. 163 days old), and old (ca. 294 days old) Aplysia for age-related changes in constituent proteins. In young, mature, and old animals protein concentrations were 1.6±0.27, 1.41±0.53, and 1.45±0.43 mg·ml-1, respectively. The copper-containing respiratory protein, hemocyanin, measured by determining the copper concentration, was found to increase significantly from young (0.98±0.51 mgrg·ml-1) to mature (2.02±0.95 mgrg·ml-1) Aplysia, with little change between mature and old (1.92±0.43 mgrg·ml-1) animals. These findings were consistent with the results obtained when hemocyanin was directly measured by spectrophotometric absorption at 340 nm. Acetylcholinesterase (AChE) was present in the hemolymph of Aplysia. Its activity was highest in mature animals (3121±1627 units·mg-1) and least in old animals (1463±599 units·mg-1). Young animals had intermediate levels (2080±762 units·mg-1). SDS-PAGE revealed a distinct pattern of protein bands for hemolymph from each age group; hemolymph from the young group contained six prominent protein bands with molecular weights (MW) from 13 to 300 kDa. Hemolymph of mature and old animals exhibited four and three prominent protein bands, respectively, with MW between 45 and 300 kDa. A prominent band at 97 kDa was present in samples from the mature group, but was faint in samples from the old group and absent in samples from the young group. Under non-denaturing conditions the hemolymph protein band patterns for each group differed from the others, thereby demonstrating that the age-dependent differences in the protein profiles are intrinsic to hemolymph in vivo. Isoelectric focusing of the hemolymph samples revealed that the proteins were all acidic (pI ca. 3.0–6.5). The hemolymph from the young differed from the other two groups in having an additional acidic protein (pI ca. 4.0). A possible link between age-related changes in hemolymph proteins and age-related changes in the nervous system is proposed.Abbreviations 2-ME 2-mercaptoethanol - AChE acetylcholinesterase - FMRFamide amidated tetrapeptide containing phenylalanine, methionine, arginine and phenylalanine - MW molecular weight - PAS periodic acid-Schiff - SDS-PAGE sodium dodecyl sulfate polyacrylamide gel electrophoresis - TRIS tris-(hydroxymethyl)-aminomethane
Keywords:Acetylcholinesterase  Aging  Hemolymph proteins  Hemocyanin  Aplysia
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