Lin S Y, Li M J, Liang R C, Lee S M
Spectrochim Acta A Mol Biomol Spectrosc. 1998 Sep;54A(10):1509-17. doi: 10.1016/s1386-1425(98)00175-9.
Previous study has supposed a possible mechanism of exacerbating cataract formation in cataractous human lens capsules induced by hypertension or glaucoma. To clarify the glaucoma-induced cataract formation of the eyes lens, changes in the human lens lipid and protein structures of immature cataractous patients with or without glaucoma were investigated. Two normal lenses, ten immature cataractous lenses without any complication and four immature cataractous lenses with glaucoma were used after surgical operation. Each de-capsulated human lens sample was sliced with a number 15 surgical blade. The intact nuclear lens regions were used for non-destructive analysis. The lens lipid and protein structures, as well as compositions of these lens samples, were determined using a Fourier transform infrared (FTIR) microspectroscopy with second-derivative, de-convolution and curve-fitting methods. The results indicate that the IR spectrum of glaucomatous lenses appeared as a shoulder only at 2853 cm-1, thus the composition of the symmetric CH2 stretching band at 2853 (2852) cm-1 decreased more significantly in glaucomatous lens to only one half of that in normal and immature cataractous lenses. The composition of the asymmetric CH3 stretching band at 2965 cm-1 for normal lens decreases markedly from 32 to 20% for immature cataractous lenses with or without glaucoma. The compositional ratio of component at 2965 cm-1 to component at 2928 (2930) cm-1 for normal lenses was about 0.702, and that ratio for cataractous lenses without glaucoma was 0.382 but for glaucomatous lenses was 0.377. The maximum peak position of amide I band for IR spectra of the normal lens, immature cataractous lenses without complications or glaucomatous lenses appeared respectively at 1632, 1630 or 1622 cm-1, assigned to beta sheet structure. A marked difference in peak intensity of amide I band for the normal lenses and immature cataractous human lenses with or without glaucoma was observed. The peak intensity ratio of amide I/amide II (1632/1545 cm-1) for normal lenses was in the range of 2.20-2.33, whereas in the spectra of immature cataractous lenses without glaucoma this ratio (1630/1545 cm-1) was 1.28-1.41 but was 1.04-1.13 for glaucomatous lens in the intensity ratio of 1622/1545 cm-1. The intensity of the glycogen bands in the wavenumber region 1135-1076 and 1069-1032 cm-1 was found to increase for the immature cataractous lenses with or without glaucoma, as compared with the normal ones. The peaks ranging from 1633 to 1610 cm-1 assigned to beta-sheet structure also exhibited a pronounced compositional difference, particularly in glaucomatous lenses. The human lens lipid and protein secondary structures were more affected by glaucoma. Higher protein side chains and reduced lipid content contributed predominantly to the CH stretching vibrations of normal lens structure, whereas high lipid content and less protein side chains dominated the CH stretching vibrations of cataractous lenses with or without glaucoma. Decrease alpha-helix and random coil structures but enhanced beta-sheet structure in the immature cataractous human lens induced by glaucoma might result from the formation of intermolecular hydrogen-bonding insoluble protein aggregates that modify the secondary structure of protein in lenses.
先前的研究推测了高血压或青光眼导致人类白内障晶状体中白内障形成加剧的一种可能机制。为了阐明青光眼导致的眼晶状体白内障形成,对患有或未患有青光眼的未成熟白内障患者的人类晶状体脂质和蛋白质结构变化进行了研究。手术切除后,使用了两枚正常晶状体、十枚无任何并发症的未成熟白内障晶状体以及四枚患有青光眼的未成熟白内障晶状体。每个去包膜的人类晶状体样本用15号手术刀片切片。完整的晶状体核区域用于无损分析。使用傅里叶变换红外(FTIR)显微光谱仪,采用二阶导数、去卷积和曲线拟合方法,测定这些晶状体样本的脂质和蛋白质结构以及组成。结果表明,青光眼晶状体的红外光谱仅在2853 cm-1处出现一个肩峰,因此,青光眼晶状体中2853(2852)cm-1处对称CH2伸缩带的组成下降更为显著,仅为正常和未成熟白内障晶状体的一半。正常晶状体在2965 cm-1处不对称CH3伸缩带的组成,对于患有或未患有青光眼的未成熟白内障晶状体,从32%显著降至20%。正常晶状体在2965 cm-1处的成分与在2928(2930)cm-1处的成分的组成比约为0.702,无青光眼的白内障晶状体的该比值为0.382,而青光眼晶状体的该比值为0.377。正常晶状体、无并发症的未成熟白内障晶状体或青光眼晶状体的红外光谱中酰胺I带的最大峰位分别出现在1632、1630或1622 cm-1处,归属于β折叠结构。观察到正常晶状体与患有或未患有青光眼的未成熟白内障人类晶状体的酰胺I带峰强度存在显著差异。正常晶状体的酰胺I/酰胺II(1632/1545 cm-1)峰强度比在2.20 - 2.33范围内,而在无青光眼的未成熟白内障晶状体光谱中,该比值(1630/1545 cm-1)为1.28 - 1.41,在青光眼晶状体光谱中,以1622/1545 cm-1的强度比为1.04 - 1.13。与正常晶状体相比,发现患有或未患有青光眼的未成熟白内障晶状体在波数区域1135 - 1076和1069 - 1032 cm-1处的糖原带强度增加。归属于β折叠结构的1633至1610 cm-1范围内的峰也表现出明显的组成差异,尤其是在青光眼晶状体中。青光眼对人类晶状体脂质和蛋白质二级结构的影响更大。较高的蛋白质侧链和较低的脂质含量主要促成了正常晶状体结构的CH伸缩振动,而较高的脂质含量和较少的蛋白质侧链主导了患有或未患有青光眼的白内障晶状体的CH伸缩振动。青光眼诱导的未成熟白内障人类晶状体中α螺旋和无规卷曲结构减少,但β折叠结构增强,这可能是由于分子间氢键不溶性蛋白质聚集体的形成,从而改变了晶状体中蛋白质的二级结构。