Hyperoxia Induces Intracellular Acidification in Neonatal Mouse Lung Fibroblasts: Real-Time Investigation Using Plasmonically Enhanced Raman Spectroscopy

被引:32
|
作者
Panikkanvalappil, Sajanlal R. [1 ]
James, Masheika [2 ]
Hira, Steven M. [1 ]
Mobley, James [3 ]
Jilling, Tamas [2 ]
Ambalavanan, Namasivayam [2 ]
El-Sayed, Mostafa A. [1 ,4 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Laser Dynam Lab, Atlanta, GA 30332 USA
[2] Univ Alabama Birmingham, Dept Pediat, Birmingham, AL 35233 USA
[3] Univ Alabama Birmingham, Dept Surg, Birmingham, AL 35233 USA
[4] King Abdulaziz Univ, Dept Chem, Jeddah 21589, Saudi Arabia
基金
美国国家科学基金会;
关键词
UNFOLDED PROTEIN RESPONSE; EXCITATION PROFILES; GOLD NANOPARTICLES; PULMONARY-FIBROSIS; OXIDATIVE STRESS; PRETERM INFANTS; OXYGEN-TOXICITY; AMINO-ACIDS; CELL-DEATH; CANCER;
D O I
10.1021/jacs.5b13177
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is important to understand the molecular mechanisms underlying oxygen toxicity, which contributes to multiple human disorders. The archetype model of oxygen toxicity is neonatal lung injury induced by hyperoxia exposure. Here, we utilized plasmonically enhanced Raman spectroscopy (PERS) in combination with fluorescence and proteomic analysis to provide comprehensive information on hyperoxia-induced biomolecular modifications in neonatal mouse lung fibroblasts (nMLFs). During this study, we made the novel observation that hyperoxia induces intracellular acidification in nMLF, which we probed in real-time using label-free PERS. We found that intracellular acidification induces conformational modifications in proteins followed by significant changes in Raman vibrations corresponding to aromatic amino acids such as phenylalanine and tryptophan as well as cysteine moieties. Hyperoxia-induced intracellular pH changes and subsequent modifications in protein expression and associated post-translational modifications within the cells were further validated by fluorescence and proteomic analysis. These new insights may help identifying unique oxidant stress-induced mechanisms in disease processes and may guide the development of more efficient therapeutic strategies.
引用
收藏
页码:3779 / 3788
页数:10
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