Van Regenmortel M H, Altschuh D, Zeder-Lutz G
Laboratoire d'Immunochimie, Institut de Biologie Moléculaire et Cellulaire du CNRS, Strasbourg, France.
Biochimie. 1993;75(8):731-9. doi: 10.1016/0300-9084(93)90104-z.
For more than 50 years, tobacco mosaic virus (TMV) has been used as a model system for studying various aspects of virus-antibody interactions. Distinct epitopes called neotopes and cryptotopes have been identified in intact TMV particles and dissociated viral protein respectively and a correlation has been found to exist between the location of continuous epitopes and the extent of segmental mobility along the viral polypeptide chain. The occurrence of bivalent antibody binding was shown to influence the observed affinity of TMV antibodies and kinetic measurements of antibody binding to viral peptides made it possible to analyze the mechanism of binding of monoclonal antibodies. It seems likely that the TMV model will continue to yield a rich harvest of immunochemical data relevant to many viral systems.
五十多年来,烟草花叶病毒(TMV)一直被用作研究病毒与抗体相互作用各个方面的模型系统。在完整的TMV颗粒和解离的病毒蛋白中分别鉴定出了称为新表位和隐蔽表位的不同表位,并且发现连续表位的位置与沿病毒多肽链的片段移动程度之间存在相关性。二价抗体结合的出现被证明会影响所观察到的TMV抗体亲和力,并且抗体与病毒肽结合的动力学测量使得分析单克隆抗体的结合机制成为可能。TMV模型似乎很可能会继续产生与许多病毒系统相关的丰富免疫化学数据。