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囊性纤维化气管支气管分泌物中一种次要粘蛋白成分的物理化学特性

Physicochemical characterization of a minor mucin component from cystic fibrosis tracheobronchial secretions.

作者信息

Padhye N V, Naziruddin B, Desai V C, Reyes de la Rocha S, Sachdev G P

机构信息

College of Pharmacy, University of Oklahoma Health Sciences Center, Oklahoma City 73190.

出版信息

Biochim Biophys Acta. 1991 Apr 29;1077(3):332-8. doi: 10.1016/0167-4838(91)90548-e.

Abstract

A minor mucin glycoprotein component (HTM-2) was purified from the tracheobronchial secretions of two cystic fibrosis patients using a protocol established in our laboratory. The secretions were solubilized in 0.1 M Tris-HCl buffer (pH 7.5) containing 0.22 M potassium thiocyanate and fractionated on a Bio-Gel A-5m column, followed by digestion with DNAase, rechromatography on the same column and chromatography on hydroxyapatite which resolved the major mucin (HTM-1) from the minor mucin component (HTM-2). The mucin component HTM-2 was further purified using Superose 6 chromatography. SDS-composite gel (2% polyacrylamide + 0.5% agarose) and 6% polyacrylamide gel electrophoresis showed that the purified HTM-2 was totally free of low-molecular-weight contaminants. Equilibrium density sedimentation centrifugation of purified HTM-2 using CsCl gradients also showed the absence of proteoglycans and other low-molecular-weight proteins. Comparison of carbohydrate and amino acid compositions of the two mucin components indicated that HTM-2 was quite different from the major mucin, HTM-1, reported earlier from our laboratory (Biochemistry, 24, 7334, 1985). This suggested that HTM-2 has a different polypeptide core and is perhaps a different gene product. The effects of 6 M guanidine-HCl and different concentrations of NaCl on the molecular size of HTM-2 and its ability to form aggregates was also investigated using the technique of static light scattering. In buffer containing 6 M guanidine-HCl, HTM-2 had a weight-average molecular weight of approximately 4.5 x 10(6). However, in the presence of buffer containing 0.03, 0.10 or 0.15 M NaCl, the molecular weight of HTM-2 was estimated to be approximately 11 x 10(6). These data suggest aggregation of HTM-2 in the presence of a range of NaCl concentrations. In contrast to HTM-1, which is a more anionic glycoprotein, the apparent molecular size of HTM-2 did not decrease at the higher NaCl concentration.

摘要

采用我们实验室建立的方法,从两名囊性纤维化患者的气管支气管分泌物中纯化出一种次要的粘蛋白糖蛋白成分(HTM-2)。分泌物溶解于含有0.22 M硫氰酸钾的0.1 M Tris-HCl缓冲液(pH 7.5)中,在Bio-Gel A-5m柱上进行分级分离,随后用DNA酶消化,在同一柱上重新色谱分离,并在羟基磷灰石柱上进行色谱分离,从而将主要粘蛋白(HTM-1)与次要粘蛋白成分(HTM-2)分离。使用Superose 6色谱法进一步纯化粘蛋白成分HTM-2。SDS复合凝胶(2%聚丙烯酰胺 + 0.5%琼脂糖)和6%聚丙烯酰胺凝胶电泳显示,纯化后的HTM-2完全不含低分子量污染物。使用CsCl梯度对纯化后的HTM-2进行平衡密度沉降离心,也表明不存在蛋白聚糖和其他低分子量蛋白质。两种粘蛋白成分的碳水化合物和氨基酸组成比较表明,HTM-2与我们实验室先前报道的主要粘蛋白HTM-1(《生物化学》,24,7334,1985)有很大不同。这表明HTM-2具有不同的多肽核心,可能是一种不同的基因产物。还使用静态光散射技术研究了6 M盐酸胍和不同浓度的氯化钠对HTM-2分子大小及其形成聚集体能力的影响。在含有6 M盐酸胍的缓冲液中,HTM-2的重均分子量约为4.5×10⁶。然而,如果存在含有0.03、0.10或0.15 M氯化钠的缓冲液,HTM-2的分子量估计约为1.1×10⁶。这些数据表明,在一定范围的氯化钠浓度下,HTM-2会发生聚集。与更具阴离子性的糖蛋白HTM-1不同,在较高氯化钠浓度下,HTM-2的表观分子大小并未减小。

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