Paul S
Department of Pathology, University of Texas Medical School, Houston, Texas 77030, USA.
Ann N Y Acad Sci. 1998 Dec 11;865:238-46. doi: 10.1111/j.1749-6632.1998.tb11183.x.
Autoantibody catalysis is now a well-established phenomenon, but the initial finding of autoantibody-catalyzed VIP cleavage was suspected to be an artefact by certain practitioners of designer antibody catalysis, mainly because of conceptual complexities not foreseen in our training about the immune system and about the mechanisms of biological catalysis. Confirmation that antibodies can acquire proteolytic activity by entirely natural means has emerged, ironically, in part from the field of designer catalytic antibodies. Recent studies have provided insight into the molecular strategies whereby antibodies can combine antigen binding with chemical catalysis, and the contributions of innate and adaptive immune mechanisms in the proteolytic activity. The history of this field illustrates the dangers of assuming that novel observations must fit into the simple confines of established theories. Scientific theories are changeable entities, dependent on empirical data and interpretations of the data, and their growth is better served by keeping an open mind.
自身抗体催化如今已是一个公认的现象,但最初发现的自身抗体催化血管活性肠肽(VIP)裂解,被某些设计抗体催化领域的从业者怀疑是一种人为现象,主要是因为在我们关于免疫系统和生物催化机制的培训中未曾预见的概念复杂性。具有讽刺意味的是,抗体可通过完全自然的方式获得蛋白水解活性这一事实的确认,部分源于设计催化抗体领域。最近的研究深入探讨了抗体将抗原结合与化学催化相结合的分子策略,以及先天免疫和适应性免疫机制在蛋白水解活性中的作用。该领域的历史说明了假定新观察结果必须符合既定理论的简单范畴所带来的危险。科学理论是可变的实体,依赖于经验数据和对数据的解释,保持开放的心态更有利于它们的发展。