EPR spectroscopy and spin-trapping methods were used to identify and monitor the formation and utilization of free radicals. The reaction of methyglyoxal and L-alanine was used as a model to study the mechanism of advanced glycation end-products formation. The results revealed that three types of free radicals were generated. They are: methyglyoxal dialkylimine radical cation, methylglyoxal radical anion and superoxide anion radical, formed only in the presence of oxygen. The study on the Cu,Zn-SOD mutant, SOD(G93A), reveals a gain-of-function, most likely by the enhancement of the free radical generating activity of the mutant, may involve developing ALS symptoms. Cytosolic Ca(II) oscillations were studied using HeLa cells. The results showed that Ca(II) oscillations are mediated by reversible phosphorylation cycles, which involve the phosphorylation of the IP3 receptor and the Ca(II) pump by CaMKII and the dephosphorylation by calyculin A inhibitable phosphatase(s). The frequency is regulated, directly or indirectly by Ins(1,3,4,5)P4, generated by IP3K, a Ca(II)- calmodulin regulated kinase. We showed that protein ubiquitinylation can be regulated by reversible phosphorylation. This involves the phosphorylation of ubiquitin activating enzyme, E1, and a number of ubiquitin carrier enzymes, E2s, by various kinases, including a novel protein kinase which phosphorylated E2-20kDa. Histochemical analysis showed that lung contains the highest activity of this kinase. Nitric oxide reacts with superoxide anion to form peroxynitrite under oxidative stress. Peroxynitrite is shown to nitrate tyrosine in protein and the nitrated tyrosine cannot serve as substrate for tyrosine kinase, such as lck kinase p56lck, a src-tyrosine kinase. These results revealed that nitration of tyrosine will seriously compromise the regulatory function of tyrosine phosphorylation. Kinetics of fluorescence indicators by electroporated cells reveals that the resealing process is accelerated by Ca(II) or a series of non-ionic synthetic surfactants in low salt medium. This effect is not as pronounced in high salt medium since resealing under this condition is fast.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Intramural Research (Z01)
Project #
1Z01HL000202-24
Application #
5203459
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
24
Fiscal Year
1995
Total Cost
Indirect Cost
Name
National Heart, Lung, and Blood Institute
Department
Type
DUNS #
City
State
Country
United States
Zip Code
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