Novak P, Dev I K
Department of Microbiology, Wellcome Research Laboratories, Research Triangle Park, North Carolina 27709.
J Bacteriol. 1988 Nov;170(11):5067-75. doi: 10.1128/jb.170.11.5067-5075.1988.
The degradation of the prolipoprotein signal peptide in vitro by membranes, cytoplasmic fraction, and two purified major signal peptide peptidases from Escherichia coli was followed by reverse-phase liquid chromatography (RPLC). The cytoplasmic fraction hydrolyzed the signal peptide completely into amino acids. In contrast, many peptide fragments accumulated as final products during the cleavage by a membrane fraction. Most of the peptides were similar to the peptides formed during the cleavage of the signal peptide by the purified membrane-bound signal peptide peptidase, protease IV. Peptide fragments generated during the cleavage of the signal peptide by protease IV and a cytoplasmic enzyme, oligopeptidase A, were identified from their amino acid compositions, their retention times during RPLC, and knowledge of the amino acid sequence of the signal peptide. Both enzymes were endopeptidases, as neither dipeptides nor free amino acids were formed during the cleavage reactions. Protease IV cleaved the signal peptide predominantly in the hydrophobic segment (residues 7 to 14). Protease IV required substrates with hydrophobic amino acids at the primary and the adjacent substrate-binding sites, with a minimum of three amino acids on either side of the scissile bond. Oligopeptidase A cleaved peptides (minimally five residues) that had either alanine or glycine at the P'1 (primary binding site) or at the P1 (preceding P'1) site of the substrate. These results support the hypothesis that protease IV is the major signal peptide peptidase in membranes that initiates the degradation of the signal peptide by making endoproteolytic cuts; oligopeptidase A and other cytoplasmic enzymes further degrade the partially degraded portions of the signal peptide that may be diffused or transported back into the cytoplasm from the membranes.
通过反相液相色谱法(RPLC)跟踪了脂蛋白信号肽在体外被膜、细胞质组分以及来自大肠杆菌的两种纯化的主要信号肽肽酶降解的过程。细胞质组分将信号肽完全水解成氨基酸。相比之下,在膜组分切割过程中,许多肽片段作为最终产物积累下来。大多数肽与纯化的膜结合信号肽肽酶蛋白酶IV切割信号肽过程中形成的肽相似。从蛋白酶IV和细胞质酶寡肽酶A切割信号肽过程中产生的肽片段的氨基酸组成、它们在RPLC中的保留时间以及信号肽的氨基酸序列信息中鉴定出了这些肽片段。这两种酶都是内肽酶,因为在切割反应过程中既没有形成二肽也没有形成游离氨基酸。蛋白酶IV主要在疏水区段(第7至14位残基)切割信号肽。蛋白酶IV需要底物在一级和相邻的底物结合位点带有疏水氨基酸,在裂解键两侧至少各有三个氨基酸。寡肽酶A切割在底物的P'1(一级结合位点)或P1(P'1之前)位点带有丙氨酸或甘氨酸的肽(最少五个残基)。这些结果支持了这样的假说:蛋白酶IV是膜中的主要信号肽肽酶,通过进行内蛋白水解切割启动信号肽的降解;寡肽酶A和其他细胞质酶进一步降解信号肽可能从膜扩散或转运回细胞质的部分降解片段。