Chernogolov A A, Usanov S A
Institute of Bioorganic Chemistry, Academy of Sciences of Belarus, Minsk, Belarus.
Biochemistry (Mosc). 1997 Dec;62(12):1385-95.
The antigenic structure of cytochrome P450scc was investigated by immunochemical identification of the peptides formed by chymotryptic cleavage of the protein and separated by reversed-phase and cation-exchange HPLCs. These procedures resulted in isolation and structural characterization of four homogeneous immunoreactive peptides which corresponded to the sequences Asn236-Tyr241, Leu266-Leu272, Ala381-Phe388, and Ser390-Trp400. These peptides contained several positively charged residues which were previously shown to participate in electrostatic interactions with adrenodoxin. Our data indicate that the positively charged residues of cytochrome P450scc are involved in formation of antigenic sites, and the antigenic determinants of the protein molecule coincide or overlap with the regions of polypeptide chain responsible for the interaction of the heme protein with adrenodoxin.
通过对细胞色素P450scc经胰凝乳蛋白酶裂解形成的肽段进行免疫化学鉴定,并采用反相和阳离子交换高效液相色谱法进行分离,研究了细胞色素P450scc的抗原结构。这些步骤导致分离并对四个同源免疫反应性肽段进行了结构表征,它们分别对应于Asn236-Tyr241、Leu266-Leu272、Ala381-Phe388和Ser390-Trp400序列。这些肽段含有几个带正电荷的残基,先前已证明这些残基参与与肾上腺铁氧化还原蛋白的静电相互作用。我们的数据表明,细胞色素P450scc带正电荷的残基参与抗原位点的形成,并且该蛋白质分子的抗原决定簇与负责血红素蛋白与肾上腺铁氧化还原蛋白相互作用的多肽链区域重合或重叠。