Hyperphosphorylated tau is a major component of neurofibrillary tangles, one of the hallmarks of Alzheimer's disease. CDK5 is a kinase that phosphorylates the tau protein, and its endogenous activator, p35, regulates its activity. Recently, calpain was found to digest p35 to its truncated product, p25. Several lines of evidence suggest that p25-CDK5 has much more powerful kinase activity and that it may cause abnormal hyperphosphorylation of tau. In this study, we have examined the kinetic characteristics of in vitro phosphorylation of the longest isoform of human tau by CDK5 and its activators using recombinant proteins. Although the kinase activity of CDK5 in phosphorylating tau was significantly higher in the presence of p25, the affinity of CDK5 for tau was not different. Aberrant phosphorylation of the tau protein is considered to play a decisive role in the pathogenesis of neurodegenerative disorders collectively called tauopathies (1). Tau is a neuronspecific, microtubule-associated protein that plays major roles in the assembly and stabilization of microtubules. In the brains of patients with Alzheimer's disease, abnormally phosphorylated tau protein, paired helical filament (PHF) 1 tau, becomes dissociated from neuronal microtubules and accumulates in PHFs, the filamentous network generated by self-aggregation of hyperphosphorylated forms of tau. All six adult isoforms of tau are known to be hyperphosphorylated in PHFs (2).Several lines of evidence suggest that proline-directed serine/threonine kinases, together with protein phosphatases, play an important role in the hyperphosphorylation of tau (3). Candidate protein kinases include mitogen-activated protein kinase, glycogen synthase kinase-3, and cyclin-dependent kinase-5 (CDK5). None of these enzymes can generate PHF-tau alone (4).CDK5, initially known as brain proline-directed protein kinase or neuronal cdc2-like protein kinase, phosphorylates tau at a high stoichiometry (5, 6). Unlike other tau kinases, the activity of CDK5 is regulated by endogenous regulatory proteins, p35 and p39. In this respect, CDK5 is distinctly different from other tau kinases (7).Recently, calpain, a calcium-dependent protease, was found to digest both p35 and p39 to their truncated products, p25 and p29, respectively (8, 9). Furthermore, truncation of p35 to p25 and the subsequent formation of the p25-CDK5 complex result in neuronal cell death and hyperphosphorylation of tau (10). From these findings, the following hypothesis emerged. Initially, various stress signals activate calpain by recruiting intracellular Ca 2ϩ , and then the activated calpain digests p35 to p25. Finally, the p25-CDK5 complex hyperphosphorylates tau proteins, causing disruption of microtubule integrity and inevitable cell death (11).Several criticisms of this hypothesis have appeared. Among them, the observed accumulation of p25 in the brains of patients with Alzheimer's disease may be accounted for by postmortem degradation of p35 (12). In fact, p35 is notoriously unstable. Most brain-derived p35...
Development of comprehensive two-dimensional packed column supercritical fluid chromatographyA comprehensive two-dimensional supercritical fluid chromatographic system with conventional packed columns was developed. The system used a computer-controlled ten-port valve, a capillary trap, and a restrictor. The mobile phase was pure carbon dioxide. The first dimension column was operated under constant pressure in the stopped-flow mode, while the second dimension column was operated in the constant flow mode. The effluent of the first column was depressurized through the restrictor and solute was trapped within the capillary trap. Then the trapped solute was transferred into the second column by switching the valve. Since the solute transfer process is very rapid, the valve can be switched back after a short injection period in order to collect next fraction. This allowed the sampling time to be changed without changing any of the other conditions, such as the second dimension run time. The system was applied to the separation of triglycerides in fats and oils. Separations were performed using the same ODS packing materials for both columns, and the first column was operated under subcritical conditions and the second column under supercritical conditions.
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