Horiuchi M, Caughey B
Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, NIAID, NIH, 903 S 4th Street, Hamilton, MT 59840, USA.
EMBO J. 1999 Jun 15;18(12):3193-203. doi: 10.1093/emboj/18.12.3193.
In the transmissible spongiform encephalopathies, normal prion protein (PrP-sen) is converted to a protease-resistant isoform, PrP-res, by an apparent self-propagating activity of the latter. Here we describe new, more physiological cell-free systems for analyzing the initial binding and subsequent conversion reactions between PrP-sen and PrP-res. These systems allowed the use of antibodies to map the sites of interaction between PrP-sen and PrP-res. Binding of antibodies (alpha219-232) to hamster PrP-sen residues 219-232 inhibited the binding of PrP-sen to PrP-res and the subsequent generation of PK-resistant PrP. However, antibodies to several other parts of PrP-sen did not inhibit. The alpha219-232 epitope itself was not required for PrP-res binding; thus, inhibition by alpha219-232 was likely due to steric blocking of a binding site that is close to, but does not include the epitope in the folded PrP-sen structure. The selectivity of the binding reaction was tested by incubating PrP-res with cell lysates or culture supernatants. Only PrP-sen was observed to bind PrP-res. This highly selective binding to PrP-res and the localized nature of the binding site on PrP-sen support the idea that PrP-sen serves as a critical ligand and/or receptor for PrP-res in the course of PrP-res propagation and pathogenesis in vivo.
在传染性海绵状脑病中,正常的朊病毒蛋白(PrP-sen)通过后者明显的自我增殖活性转化为蛋白酶抗性异构体PrP-res。在此,我们描述了用于分析PrP-sen和PrP-res之间初始结合及后续转化反应的新型、更具生理性的无细胞系统。这些系统允许使用抗体来定位PrP-sen和PrP-res之间的相互作用位点。抗体(α219-232)与仓鼠PrP-sen的219-232位残基结合会抑制PrP-sen与PrP-res的结合以及随后PK抗性PrP的产生。然而,针对PrP-sen其他几个部位的抗体则没有抑制作用。PrP-res结合并不需要α219-232表位本身;因此,α219-232的抑制作用可能是由于在折叠的PrP-sen结构中靠近但不包括该表位的结合位点受到空间位阻。通过将PrP-res与细胞裂解物或培养上清液孵育来测试结合反应的选择性。仅观察到PrP-sen与PrP-res结合。这种与PrP-res的高度选择性结合以及PrP-sen上结合位点的局限性支持了这样一种观点,即PrP-sen在PrP-res体内传播和发病过程中作为PrP-res的关键配体和/或受体。