Vogel Carl-Wilhelm
Cancer Research Center of Hawaii, University of Hawaii, Honolulu, USA.
Methods Mol Biol. 2004;283:87-108. doi: 10.1385/1-59259-813-7:087.
Heterobifunctional crosslinking reagents are small molecular weight chemicals containing two different reactive groups that have become important tools in generating conjugates of two different biomolecules, such as two proteins. The resulting bioconjugates are hybrid molecules or proteins, a new category of biomolecules that exhibit the combined functions of the two parent biomolecules. An important category of hybrid proteins are conjugates of antibodies with other effector molecules, such as drugs or toxins. These antibody conjugates or immunoconjugates have a variety of the applications in medicine, with particular emphasis on the treatment of cancer. The most commonly used heterobifunctional crosslinking reagents for the synthesis of antibody conjugates contain an N-hydroxysuccinimide ester moiety, which allows derivatization of amino groups in proteins. The chemical modification of a functionally important amino group in the antigen-binding region of an antibody causes impairment or loss of the antigen binding function, resulting in a defective antibody conjugate that lacks one of its component functions. Furthermore, even if the chemical derivatization does not affect the antigen binding function, the subsequent coupling of an effector protein at or near the antigen-binding region can also cause the loss of the antigen binding function for steric reasons. In this chapter, heterobifunctional crosslinking reagents are described that allow the generation of antibody conjugates where the effector proteins are coupled to the antibody carbohydrate moieties. Because antibody carbohydrate moieties are distal from the antigen-binding region, the use of carbohydrate-directed heterobifunctional crosslinking reagents, such as S-(2-thiopyridyl)-L-cysteine hydrazide (TPCH), prevents inactivation of the antigen-binding function. The synthesis of two carbohydrate-directed heterobifunctional crosslinking reagents is described. Coupling protocols for the preparation of antibody conjugates with effector proteins of different sizes using carbohydrate-directed heterobifunctional crosslinking reagents are also provided.
异双功能交联剂是一类小分子化学物质,含有两个不同的反应基团,已成为生成两种不同生物分子(如两种蛋白质)共轭物的重要工具。所得的生物共轭物是杂合分子或蛋白质,这是一类新的生物分子,展现出两种亲本生物分子的综合功能。一类重要的杂合蛋白质是抗体与其他效应分子(如药物或毒素)的共轭物。这些抗体共轭物或免疫共轭物在医学上有多种应用,尤其侧重于癌症治疗。用于合成抗体共轭物最常用的异双功能交联剂含有N - 羟基琥珀酰亚胺酯部分,它能使蛋白质中的氨基进行衍生化。抗体抗原结合区域中功能重要的氨基发生化学修饰会导致抗原结合功能受损或丧失,从而产生缺乏其一种组成功能的有缺陷的抗体共轭物。此外,即使化学衍生化不影响抗原结合功能,效应蛋白在抗原结合区域或其附近的后续偶联也可能由于空间位阻原因导致抗原结合功能丧失。在本章中,将描述能生成效应蛋白与抗体碳水化合物部分偶联的抗体共轭物的异双功能交联剂。由于抗体碳水化合物部分远离抗原结合区域,使用碳水化合物定向的异双功能交联剂,如S -(2 - 吡啶硫基)-L - 半胱氨酸酰肼(TPCH),可防止抗原结合功能失活。文中描述了两种碳水化合物定向的异双功能交联剂的合成方法。还提供了使用碳水化合物定向的异双功能交联剂制备与不同大小效应蛋白的抗体共轭物的偶联方案。