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The carboxylmethylation of cerebral membrane-bound proteins increases with age

O Z Sellinger1, C M Kramer, A Conger

  • 1Mental Health Research Institute, University of Michigan Medical Center, Ann Arbor 48109.

Insights

Brain membrane proteins become more methylated with age, indicating structural changes. This age-related increase in methylation suggests modifications in membrane-bound methyl-accepting proteins (MAPs) during neural aging.

Area of Science:

  • Neuroscience
  • Biochemistry
  • Molecular Biology

Background:

  • Brain protein carboxylmethyltransferase II (PCMT) methylates membrane-bound methyl-accepting proteins (MAPs).
  • Alkali treatment increases PCMT recognition of mb-MAPs, likely by forming isoaspartate residues from asparagine/aspartate deamidation.
  • This suggests isoaspartate residues are key targets for PCMT in membrane-bound MAPs.

Purpose of the Study:

  • To investigate age-related changes in membrane-bound MAPs in rat brains.
  • To determine if isoaspartate formation contributes to age-related changes in mb-MAPs.

Main Methods:

  • Prepared and purified synaptic membranes from young (3-4 months) and old (11-12 months) rat brains.
  • Measured carboxyl[3H]methylation of mb-MAPs using [3H]methyl S-adenosyl-L-methionine.
  • Treated young and old membranes/extracts with ammonium hydroxide (NH4OH) to assess carboxylmethylatable site generation.

Main Results:

  • Carboxymethylation of mb-MAPs was significantly higher in membranes from old rats compared to young rats.
  • This age-related increase in methylation was confirmed across various protein concentrations and incubation times.
  • Alkaline treatment generated fewer new carboxylmethylatable sites in proteins from old rats than in those from young rats.

Conclusions:

  • Age-related modifications in the primary structure of susceptible mb-MAPs lead to increased carboxylmethylation.
  • The reduced generation of new carboxylmethylatable sites in older proteins suggests that these sites are formed in situ during neural aging.
  • These findings highlight the role of protein modifications and isoaspartate formation in the aging of neural membrane proteins.

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