4.7 Article

Analysis of mitochondrial oxygen consumption and hydrogen peroxide release from cardiac mitochondria using electrochemical multi-sensors

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 360, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2022.131641

关键词

Enzymatic sensor; Hydrogen peroxide sensor; Oxygen sensor; Mitochondria; Biosensors

资金

  1. National Science Foundation (USA) [0841259, 1450032]
  2. Division Of Graduate Education
  3. Direct For Education and Human Resources [0841259] Funding Source: National Science Foundation

向作者/读者索取更多资源

Mitochondria are vital for oxygen consumption and energy metabolism in cells, but also produce reactive oxygen species (ROS) with various effects. This paper presents a sensitive multi-sensor device capable of measuring ROS production and oxygen consumption rate (OCR) simultaneously in biological samples. The device has been validated in scarce biological samples and shows potential utility in studying cellular metabolism and mitochondrial function.
Mitochondria are the primary sites of oxygen (O2) consumption and energy metabolism in most cell types, but also produce reactive oxygen species (ROS) that contribute to a wide array of pathological and physiological processes. Accordingly, simultaneous monitoring of mitochondrial ROS release and oxygen consumption rate (OCR) from cells and mitochondrial preparations is an attractive investigative approach in biological research, particularly when sample quantity is scarce. This paper presents the development of a sensitive multi-sensor device capable of measuring ROS production and OCR from biological samples in a single micro-chamber assay. Sensor sensitivities for O2 and hydrogen peroxide (H2O2; the major ROS species released by mitochondria and cells) are 4.32 nA/mu M and 54.89 nA/mu M, respectively, with limits of detection of 2.9 mu M and 58.36 nM, respectively. Proof-of-concept studies in isolated mitochondria from rat cardiac tissue (5 mu g protein) demonstrate an expected 3 - 4 fold increase in H2O2 release over the basal rate following addition of respiratory substrates, with a comparatively small change in OCR. The subsequent addition of adenosine diphosphate (ADP) decreased H2O2 release by 73% (p < 0.01) and increased OCR by 168% (p < 0.01), consistent with established shifts in mitochondrial membrane potential and electron flow from an ADP-limited (State 4) to ADP-stimulated (State 3) respiratory state. These studies validate the results from the use of a novel multi-sensor device capable of monitoring OCR and H2O2 simultaneously in scarce biological samples, with potential utility in the nondestructive integrative study of cellular metabolism and mitochondrial function.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据