Related Experiment Videos
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.
Abstract:
Recently, we have characterized a membrane-bound (mb) component of brain protein carboxylmethyltransferase II (PCMT) which effectively carboxylmethylates endogenous mb methyl-accepting proteins (MAPs). (Neurochem. Int., 10 (1987) 155). We have also shown that exposing mb-MAPs to mild alkali leads to a marked increase in their recognition by PCMT. Since one of the likely consequences of the alkaline treatment appears to be the deamidation of selected protein-bound asparagines or aspartates, followed by the formation, in their place, of D-or L-isoaspartates, it is reasonable to assume that mb-MAPs constitute unique targets for the mb-PCMT because they contain such unnatural aspartate residues. Testing the relevance of this notion to the aging of cerebral mb-MAPs we focus in this report on age-related changes involving mb-MAPs. When two-or six-times washed (in 50 mM NaPO4 buffer, pH 6.5) 17,500 g, 30-min membranes or Percoll-gradient purified synaptic membranes were prepared from young (3-4 months) and old (11-12 months) rat brains and were incubated with 20 microM [3H]methyl S-adenosyl-L-methionine at pH 6.0, mb-MAP carboxyl[3H]methylation was significantly more intense in the old than in the young membranes, no additional increase being noted at 28-35 months. Mb-MAP carboxylmethylation increases were confirmed over a wide range of membrane protein concentrations and incubation times and are taken to reflect age-related modifications of the primary structure of susceptible mb-MAPs. To investigate these, we incubated young and old membranes, as well as their Lubrol-Px (1%) extracts (30 min, 0 degree C), with 0.05 M NH4OH for 90 min at 37 degrees C, a treatment which left PCMT activity largely unaffected. Our findings reveal that the effect of the NH4OH treatment on the generation of carboxylmethylatable sites was markedly smaller in "old" than in "young" proteins, suggesting that "new" carboxylmethylatable sites are generated in susceptible mb-MAPs in situ, by a process accompanying, or otherwise marking, the natural aging of neural membrane proteins.
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.