Sellinger O Z, Kramer C M, Conger A, Duboff G S
Mental Health Research Institute, University of Michigan Medical Center, Ann Arbor 48109.
Mech Ageing Dev. 1988 May;43(2):161-73. doi: 10.1016/0047-6374(88)90044-9.
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.
最近,我们已鉴定出脑蛋白羧甲基转移酶II(PCMT)的一种膜结合(mb)成分,它能有效地将内源性mb甲基受体蛋白(MAPs)羧甲基化。(《神经化学国际》,10(1987)155)。我们还表明,将mb-MAPs暴露于弱碱中会导致PCMT对它们的识别显著增加。由于碱处理的一个可能后果似乎是选定的蛋白质结合天冬酰胺或天冬氨酸脱酰胺,随后在其位置形成D-或L-异天冬氨酸,因此有理由假设mb-MAPs构成mb-PCMT的独特靶点,因为它们含有这种非天然的天冬氨酸残基。为了检验这一概念与脑mb-MAPs衰老的相关性,在本报告中,我们关注涉及mb-MAPs的与年龄相关的变化。当从年轻(3 - 4个月)和年老(11 - 12个月)大鼠脑制备的17,500 g、30分钟的膜或Percoll梯度纯化的突触膜用50 mM NaPO4缓冲液(pH 6.5)洗涤2次或6次后,在pH 6.0下与20 microM [3H]甲基S-腺苷-L-甲硫氨酸孵育时,年老膜中mb-MAP羧基[3H]甲基化明显比年轻膜强烈,在28 - 35个月时未观察到进一步增加。在广泛的膜蛋白浓度和孵育时间范围内均证实了mb-MAP羧甲基化增加,这被认为反映了易感mb-MAPs一级结构的与年龄相关的修饰。为了研究这些,我们将年轻和年老的膜及其Lubrol-Px(1%)提取物(30分钟,0℃)在37℃下用0.05 M NH4OH孵育90分钟,该处理对PCMT活性影响不大。我们的研究结果表明,NH4OH处理对可羧甲基化位点产生的影响在“年老”蛋白质中明显小于“年轻”蛋白质,这表明在易感mb-MAPs中原位产生“新的”可羧甲基化位点,是伴随神经膜蛋白自然衰老的一个过程,或以其他方式标记该过程。