Brunisholz R A, Wiemken V, Suter F, Bachofen R, Zuber H
Hoppe Seylers Z Physiol Chem. 1984 Jul;365(7):689-701. doi: 10.1515/bchm2.1984.365.2.689.
The unspecific proteinase K and the specific proteases alpha-chymotrypsin, trypsin and S. aureus V 8 protease were used in order to determine the orientation of the polypeptides B 870-alpha and B 870-beta from the major antenna complex B 870 of Rs. rubrum G-9+ within the chromatophore membrane (inside-out vesicle). Although B 870-alpha exhibits cleavable peptide bonds, treatment with specific proteases yielded splitting only in B 870-beta within the N-terminal region. In the case of proteinase K, which was most effective, mainly 6 (B 870-alpha) and 16 (B 870-beta) amino acid residues were removed from their N-terminal parts as proved by means of Edman degradation of cleavage products. The major peptide bonds cleaved were identified as Gln6-Leu7 in B 870-alpha and as Lys16-Glu17 in B 870-beta. The central hydrophobic stretch regions and the relatively hydrophilic C-terminal parts of both light-harvesting polypeptides were not affected by proteinase K. On the basis of these degradation experiments a transmembrane orientation of B 870-alpha and B 870-beta is postulated, with their N-terminal towards the cytoplasm and their C-termini towards periplasm with regard to the photosynthetic membrane. This hypothesis is supported by the transmembrane model proposed by Brunisholz et al. (Hoppe-Seyler's Z., Physiol. Chem., (1984) 365, 675-688) in which the hydrophobic stretch of B 870-alpha and of B 870-beta forming an alpha-helix would span the membrane once. Organic solvent extraction of chromatophores treated with proteinase K yielded a fairly pure polypeptide fragment with an apparent molecular mass of 14000 Da. Its N-terminal amino-acid sequence is identical with the sequence within the N-terminal region of the reaction centre subunit L of Rs. rubrum G-9+. Thus it is most likely that as in the case of B 870-beta, proteinase K removed 16 amino acid residues from the N-terminal part of subunit L. This subunit therefore also seems to be exposed at the surface of the cytoplasmic side of the chromatophore membrane.
为了确定来自深红螺菌G-9 +主要天线复合物B 870的多肽B 870-α和B 870-β在色素体膜(内翻囊泡)中的方向,使用了非特异性蛋白酶K和特异性蛋白酶α-胰凝乳蛋白酶、胰蛋白酶和金黄色葡萄球菌V 8蛋白酶。尽管B 870-α表现出可切割的肽键,但用特异性蛋白酶处理仅在N端区域的B 870-β中产生了裂解。在最有效的蛋白酶K的情况下,通过对裂解产物进行埃德曼降解证明,主要从它们的N端部分去除了6个(B 870-α)和16个(B 870-β)氨基酸残基。裂解的主要肽键在B 870-α中被鉴定为Gln6-Leu7,在B 870-β中被鉴定为Lys16-Glu17。两种捕光多肽的中央疏水延伸区域和相对亲水的C端部分均不受蛋白酶K的影响。基于这些降解实验,推测B 870-α和B 870-β具有跨膜方向,就光合膜而言,它们的N端朝向细胞质,C端朝向周质。这一假设得到了Brunisholz等人提出的跨膜模型(Hoppe-Seyler's Z., Physiol. Chem., (1984) 365, 675 - 688)的支持,在该模型中,形成α-螺旋的B 870-α和B 870-β的疏水延伸将跨膜一次。用蛋白酶K处理的色素体的有机溶剂提取产生了一个表观分子量为14000 Da的相当纯的多肽片段。其N端氨基酸序列与深红螺菌G-9 +反应中心亚基L的N端区域内的序列相同。因此,很可能与B 870-β的情况一样,蛋白酶K从亚基L的N端部分去除了16个氨基酸残基。因此,该亚基似乎也暴露在色素体膜细胞质侧的表面。