“…NAD(P) + and NAD(P)H, respectively) ( Fig. 1) can provide information on the effect of dietary factors or drug candidates [2]. One of the most important coenzymes in hydride transfer reactions is nicotinamide adenine dinucleotide (NAD + ).…”
Section: Metabolism and Roles Of Pyridine Nucleotidesmentioning
confidence: 99%
“…cer.) [9,31,32], and Methylobacterium extorquens AM1 [33] was monitored, and whole blood [2,12], serum and plasma [6,7,34] urine [6], cultured cells [6-9, 30, 34, 35], cerebrospinal fluid [34], and tissues [4,6,7,31,34] were used as samples.…”
Section: Analysis Of Endogenous Pyridine Dinucleotidesmentioning
confidence: 99%
“…Caruso et al investigated the preanalytical phase of blood adenine and pyridine nucleotide determination [2]. They performed a double extraction method and two different chromatographic runs for reduced and oxidized forms of nucleotides.…”
Section: Analysis Of Endogenous Pyridine Dinucleotidesmentioning
confidence: 99%
“…Severe disturbance in the redox balance, e.g. oxidative stress, which is often caused by an external impact is an important component of the pathomechanism of cardiovascular diseases such as heart failure, myocardial ischemia, unstable angina and ischemia reperfusion injury [2]. The largely autonomous redox homeostasis of the endoplasmic reticulum (ER) is based on the co-localization of a reduced pyridine dinucleotide NAD(P) + /NAD(P)H system and an oxidized thiol-disulfide system.…”
Section: Introductionmentioning
confidence: 99%
“…This ER stress stimulates a complex signalling network referred to as the unfolded protein response (UPR), which is primarily adaptive, but it can also lead to different destructive downstream effects including inflammations, apoptosis and insulin resistance [3]. Ratio of oxidized and reduced forms of pyridine dinucleotides gives precious information about redox metabolism disorders or energetic alterations [2]. Thus, precise measurement of these nucleotides has become essential.…”
“…NAD(P) + and NAD(P)H, respectively) ( Fig. 1) can provide information on the effect of dietary factors or drug candidates [2]. One of the most important coenzymes in hydride transfer reactions is nicotinamide adenine dinucleotide (NAD + ).…”
Section: Metabolism and Roles Of Pyridine Nucleotidesmentioning
confidence: 99%
“…cer.) [9,31,32], and Methylobacterium extorquens AM1 [33] was monitored, and whole blood [2,12], serum and plasma [6,7,34] urine [6], cultured cells [6-9, 30, 34, 35], cerebrospinal fluid [34], and tissues [4,6,7,31,34] were used as samples.…”
Section: Analysis Of Endogenous Pyridine Dinucleotidesmentioning
confidence: 99%
“…Caruso et al investigated the preanalytical phase of blood adenine and pyridine nucleotide determination [2]. They performed a double extraction method and two different chromatographic runs for reduced and oxidized forms of nucleotides.…”
Section: Analysis Of Endogenous Pyridine Dinucleotidesmentioning
confidence: 99%
“…Severe disturbance in the redox balance, e.g. oxidative stress, which is often caused by an external impact is an important component of the pathomechanism of cardiovascular diseases such as heart failure, myocardial ischemia, unstable angina and ischemia reperfusion injury [2]. The largely autonomous redox homeostasis of the endoplasmic reticulum (ER) is based on the co-localization of a reduced pyridine dinucleotide NAD(P) + /NAD(P)H system and an oxidized thiol-disulfide system.…”
Section: Introductionmentioning
confidence: 99%
“…This ER stress stimulates a complex signalling network referred to as the unfolded protein response (UPR), which is primarily adaptive, but it can also lead to different destructive downstream effects including inflammations, apoptosis and insulin resistance [3]. Ratio of oxidized and reduced forms of pyridine dinucleotides gives precious information about redox metabolism disorders or energetic alterations [2]. Thus, precise measurement of these nucleotides has become essential.…”
The pyridine nucleotides NAD(H) and NADP(H) are key molecules in cellular metabolism and measuring their levels and oxidation states with spatiotemporal precision is of great value in biomedical research. Traditional methods to assess the redox state of these metabolites are intrusive and prohibit live-cell quantifications. This obstacle was surpassed by the development of genetically encoded fluorescent biosensors enabling dynamic measurements with subcellular 2 resolution in living cells. Here, we provide step-by-step protocols to monitor the intraperoxisomal NADPH levels and NAD + /NADH redox state in cellulo by using targeted variants of iNAP1 and SoNar, respectively.
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