Dubbelman T M, De Goeij A F, Van Steveninck J
Biochim Biophys Acta. 1980;595(1):133-9. doi: 10.1016/0005-2736(80)90255-2.
Previous studies have shown that illumination of erythrocytes with visible light in the presence of protoporphyrin results in cross-linking of membrane proteins and deterioration of several membrane functions, e.g. active transport of K+ and Na+. In the present study it is shown that carrier-mediated transport of glucose, L-leucine, sulphate and glycerol is also inhibited by the photodynamic process, whereas non-specific permeability of glycerol and thiourea is increased. It is shown that these effects are not caused by lipid peroxidation, but by photooxidation of membrane proteins. The inhibition of carrier-mediated transport is caused either by photodynamic oxidation of susceptible essential amino acid residues of the carrier molecules, or by an aspectific perturbation of the membrane structure, leading to inhibition of carrier functions.
先前的研究表明,在原卟啉存在的情况下,用可见光照射红细胞会导致膜蛋白交联以及多种膜功能的恶化,例如钾离子和钠离子的主动转运。在本研究中发现,光动力过程也会抑制葡萄糖、L-亮氨酸、硫酸盐和甘油的载体介导转运,而甘油和硫脲的非特异性通透性会增加。结果表明,这些效应不是由脂质过氧化引起的,而是由膜蛋白的光氧化导致的。载体介导转运的抑制要么是由于载体分子中敏感必需氨基酸残基的光动力氧化,要么是由于膜结构的非特异性扰动,从而导致载体功能受到抑制。