Beachey E H, Seyer J M, Dale J B, Hasty D L
J Biol Chem. 1983 Nov 10;258(21):13250-7.
The complete amino acid sequences of three cyanogen bromide peptide fragments (CB3, CB4, and CB50 of type 24 M protein extracted from Streptococcus pyogenes by limited pepsin digestion were determined by automated Edman degradation of the uncleaved peptides and their tryptic peptides. CB3 and CB4 each contain 35 amino acid residues, whereas CB5 contains 37. The sequence of CB3 was found to be: (formula: see text) (where Hse represents homoserine). The sequence of CB4 was identical except for amino acid substitutions of arginine and glutamine at positions 23 and 24, respectively. The sequence of CB5 also was identical with that of CB3 except for substitutions of aspartic acids at positions 28 and 29; leucine, glutamic acid, and glycine at positions 33, 34, and 35, respectively; and an additional two amino acids, alanine and homoserine, at positions 36 and 37, respectively. A comparison of the structures of these three peptide fragments with those previously reported for CB6 and CB7 revealed as few as one to six amino acid substitutions among the five repeating peptides; CB4 and CB6 differed only by a single Asp/Glu substitution at position 26. When covalently linked to polylysine and injected as an emulsion in complete Freund's adjuvant, CB3, CB4, and CB5 each evoked high titers of type-specific opsonic and bactericidal antibodies in rabbits. A chemically synthesized peptide identical with native CB3 except that it contained methionine instead of homoserine at its COOH terminus was similarly immunogenic. None of the conjugated native or synthetic peptides raised antibodies at reacted in immunofluorescence tests with sarcolemmal membranes of human heart tissue. Mapping studies with monoclonal antibodies revealed a number of distinct protective and nonprotective epitopes. The single Asp/Glu substitution between CB4 and CB4 rendered the 35-residue peptide unrecognizable by protective monoclonal antibodies but recognizable by a nonprotective one. Our studies demonstrate that the repeating covalent structures of native and chemically synthesized polypeptide fragments of streptococcal M protein possess several unique as well as repeating epitopes that evoke opsonic and presumably protective, but not heart cross-reactive, antibodies against a rheumatogenic strain of S. pyogenes.
通过对未切割肽段及其胰蛋白酶肽段进行自动Edman降解,测定了经有限胃蛋白酶消化从化脓性链球菌中提取的24型M蛋白的三个溴化氰肽片段(CB3、CB4和CB5)的完整氨基酸序列。CB3和CB4各含35个氨基酸残基,而CB5含37个。发现CB3的序列为:(分子式:见正文)(其中Hse代表高丝氨酸)。CB4的序列除分别在第23和24位的精氨酸和谷氨酰胺发生氨基酸替换外与CB3相同。CB5的序列也与CB3相同,只是在第28和29位的天冬氨酸、第33、34和35位的亮氨酸、谷氨酸和甘氨酸分别被替换,并且在第36和37位分别额外增加了两个氨基酸丙氨酸和高丝氨酸。将这三个肽片段的结构与先前报道的CB6和CB7的结构进行比较,发现在这五个重复肽段中氨基酸替换少至一到六个;CB4和CB6仅在第26位有一个天冬氨酸/谷氨酸的单一替换不同。当与聚赖氨酸共价连接并作为乳剂注射到完全弗氏佐剂中时,CB3、CB4和CB5在兔体内均能诱导体液中高滴度的型特异性调理和杀菌抗体。一种化学合成肽,除了在其COOH末端含甲硫氨酸而非高丝氨酸外与天然CB3相同,同样具有免疫原性。无论是天然的还是合成的偶联肽,均未产生能与人心脏组织肌膜在免疫荧光试验中发生反应的抗体。用单克隆抗体进行的定位研究揭示了许多不同的保护性和非保护性表位。CB4和CB6之间的单一天冬氨酸/谷氨酸替换使这个35个残基的肽不能被保护性单克隆抗体识别,但能被一个非保护性单克隆抗体识别。我们的研究表明,化脓性链球菌M蛋白的天然和化学合成多肽片段的重复共价结构具有几个独特的以及重复的表位,这些表位能诱导体液中针对化脓性链球菌致风湿菌株的调理抗体以及推测的保护性抗体,但不产生与心脏交叉反应的抗体。