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糖胺聚糖的构象及高碘酸盐氧化后的变化

Glycosaminoglycan conformations and changes on periodate oxidation.

作者信息

Ueno N, Chakrabarti B

出版信息

Biopolymers. 1989 Nov;28(11):1891-902. doi: 10.1002/bip.360281106.

Abstract

The progressive periodate oxidation of glycosaminoglycans (GAG), including hyaluronate (HA), chondroitins (CH) (chondroitin, chondroitin 4- and 6-sulfate), dermatan sulfate (DS), and keratan sulfate (KS), were monitored by CD and high performance liquid chromatography (HPLC) using a size-exclusion column. The rate of oxidation also was measured and calculated using first- and second-order kinetics, and the data appear to fit better with first-order kinetics. In both HA and CH, the n - pi amide band at 208 nm decreases in intensity upon oxidation, but in HA it becomes positive after 16 h of periodate treatment. In CH, the band disappears, and the pi - pi amide band below 200 nm becomes optically active. Concomitantly, a second negative band near 290 nm appears for these two oxidized GAG. Oxidation causes a slight change in the CD of DS. It ordinarily displays a very weak n - pi band at 210 nm, but instead shows an intense pi - pi amide band near 190 nm. CD of KS remains unaffected by periodate. Kinetic studies, however, show a higher oxidation rate for DS than HA and CH. With the exception of KS, all other oxidized polymers shown an apparent decrease in molecular weight (higher peak retention time) in HPLC analysis. Both CD and HPLC results have been attributed to a major conformational change of HA and CH, and a minor one for DS. The ease and extent of periodate oxidation as well as the changes in molecular properties following periodate treatment are critically dependent on the configuration of the individual GAG rather than the oxidation rate. There is a distinct difference in the conformational change between HA and CH, as manifested by their dichroic behavior, that was attributed to the equatorial disposition of C-4 hydroxyl group in HA and axial disposition CH.

摘要

通过圆二色光谱(CD)和使用尺寸排阻柱的高效液相色谱法(HPLC)监测了包括透明质酸(HA)、软骨素(CH)(软骨素、硫酸软骨素4-硫酸盐和6-硫酸盐)、硫酸皮肤素(DS)和硫酸角质素(KS)在内的糖胺聚糖(GAG)的渐进高碘酸盐氧化过程。氧化速率也采用一级和二级动力学进行了测量和计算,数据似乎更符合一级动力学。在HA和CH中,208 nm处的n-π酰胺带在氧化后强度降低,但在HA中,高碘酸盐处理16小时后变为正值。在CH中,该带消失,200 nm以下的π-π酰胺带变得具有光学活性。同时,这两种氧化的GAG在290 nm附近出现第二个负带。氧化导致DS的CD略有变化。它通常在210 nm处显示一个非常弱的n-π带,但取而代之的是在190 nm附近显示一个强烈的π-π酰胺带。KS的CD不受高碘酸盐影响。然而,动力学研究表明DS的氧化速率高于HA和CH。除KS外,所有其他氧化聚合物在HPLC分析中均显示分子量明显降低(保留时间峰更高)。CD和HPLC结果均归因于HA和CH的主要构象变化以及DS的次要构象变化。高碘酸盐氧化的难易程度和程度以及高碘酸盐处理后分子性质的变化严重依赖于各个GAG的构型而非氧化速率。HA和CH之间的构象变化存在明显差异,这通过它们的二色性行为表现出来,这归因于HA中C-4羟基的赤道取向和CH中C-4羟基的轴向取向。

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