Walker B, Krishnasastry M, Bayley H
Worcester Foundation for Experimental Biology, Shrewsbury, MA 01545.
J Biol Chem. 1993 Mar 5;268(7):5285-92.
The final steps in assembly of the lytic pore formed by staphylococcal alpha-hemolysin (alpha HL) involve the formation of a nonlytic oligomeric pore precursor, followed by the formation of a transmembrane channel. In this study, truncation mutants of alpha HL encompassing the NH2-terminal or COOH-terminal half of the polypeptide chain and all, part, or none of the central glycine-rich loop were obtained by in vitro, coupled transcription and translation of mutant plasmid DNAs. These polypeptides were unable to oligomerize upon or cause lysis of rabbit erythrocytes (rRBCs). Twenty-one pairs of the same truncation mutants constituting discontinuous alpha HL chains with overlaps, nicks, and gaps in the central loop were obtained by cotranslation. When incubated with rRBCs, many of the pairs were able to form hetero-oligomers with wild-type alpha-hemolysin (s-alpha HL) and most of these formed homo-oligomers in the absence of s-alpha HL. However, only members of a subset of these pairs were able to lyse the cells. The lytic combinations contained overlaps, nicks, or gaps, but only two pairs, with nicks between amino acid residues 128 and 129 and between 131 and 132 had hemolytic activities approaching that of the wild-type polypeptide. Active combinations could also be obtained by separately translating NH2- and COOH-terminal truncation mutants and then combining them. These findings suggest that the integrity of the central loop is of little significance for oligomer formation but that it is more important for the final step in pore assembly or alternatively for determining the correct structure of the conductive channel. Our findings disagree with previous reports of NH2- and COOH-terminal fragments with hemolytic activity and of the prevention of hemolysis by proteolytic cleavage in the central loop. This discord is attributed to experimental and interpretative ambiguities in the earlier protein chemistry. For example, we show that loss of hemolytic activity after treatment with trypsin is not due to cleavage after Lys-131, as previously proposed, but to the removal of a small NH2-terminal peptide through cleavage after Lys-8.
由葡萄球菌α-溶血素(αHL)形成的裂解孔组装的最后步骤包括形成非裂解性寡聚孔前体,随后形成跨膜通道。在本研究中,通过对突变体质粒DNA进行体外偶联转录和翻译,获得了αHL的截短突变体,这些突变体涵盖多肽链的NH2末端或COOH末端一半以及中央富含甘氨酸环的全部、部分或无。这些多肽不能在兔红细胞(rRBCs)上寡聚化或导致其裂解。通过共翻译获得了21对相同的截短突变体,它们构成了中央环有重叠、切口和间隙的不连续αHL链。当与rRBCs一起孵育时,许多对能够与野生型α-溶血素(s-αHL)形成异源寡聚体,并且其中大多数在没有s-αHL的情况下形成同源寡聚体。然而,只有这些对中的一个子集的成员能够裂解细胞。裂解组合包含重叠、切口或间隙,但只有两对,在氨基酸残基128和129之间以及131和132之间有切口,其溶血活性接近野生型多肽。通过分别翻译NH2-和COOH-末端截短突变体然后将它们组合也可以获得活性组合。这些发现表明中央环的完整性对寡聚体形成意义不大,但对孔组装的最后步骤或确定导电通道的正确结构更重要。我们的发现与先前关于具有溶血活性的NH2-和COOH-末端片段以及中央环中蛋白水解切割可防止溶血的报道不一致。这种不一致归因于早期蛋白质化学中的实验和解释模糊性。例如,我们表明用胰蛋白酶处理后溶血活性的丧失不是如先前提出的那样由于Lys-131之后的切割,而是由于Lys-8之后的切割去除了一个小的NH2-末端肽。