Brewer C F, Brown R D, Koenig S H
Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York 10461.
J Biomol Struct Dyn. 1983 Dec;1(4):961-97. doi: 10.1080/07391102.1983.10507497.
The affinity of the lectin Concanavalin A (Con A) for saccharides, and its requirement for metal ions such as Mn2+ and Ca2+, have been known for about 50 years. However the relationship between metal ion binding and the saccharide binding activity of Con A has only recently been examined in detail. Brown et al. (Biochemistry 16, 3883 (1977)) showed that Con A exists as a mixture of two conformational states: a "locked" form and an "unlocked" form. The unlocked form of the protein weakly binds metal ions and saccharide, and is the predominate conformation of demetallized Con A (apo-Con A) at equilibrium. The locked form binds two metal ions per monomer with the resulting complex(es) possessing full saccharide binding activity. Brown and coworkers measured the kinetics of the transition of the unlocked form to the fully metallized locked conformation containing Mn2+ and Ca2+. They also demonstrated that Mn2+ alone could form a locked ternary complex with Con A, and that rapid removal of the ions resulted in a metastable form of apo-Con A in the locked conformation which slowly (hours at 25 degrees C) reverted back to (predominantly) the unlocked conformation. The ability to form either conformation in the absence or presence of metal ions has thus allowed us to explore the relationship between metal ion binding and conformational transitions in Con A as determinants of the saccharide binding activity of the lectin. Based on the kinetics of the transition of unlocked apo-Con A to fully metallized locked Con A, and X-ray crystallographic data, it appears that the transition between the two conformations of Con A involves a cis-trans isomerization of an Ala-Asp peptide bond in the backbone of the protein, near one of the two metal ion binding sites. The relatively large activation energy for the transition (approximately 22 kcal M-1) results in relatively slow interconversions between the conformations (from minutes to days), whereas the equilibria with metal ions and saccharide are rapid. Thus, many metastable complexes can be formed and a variety of transition pathways between the two conformations studied. We have identified and characterized binary, ternary, and quaternary complexes of both conformations of Con A containing Mn2+ and saccharide, and have determined both metal ion and saccharide dissociation constants for all of them, as well as equilibrium and kinetic values for the conformational transitions between them.(ABSTRACT TRUNCATED AT 400 WORDS)
伴刀豆球蛋白A(Con A)对糖类的亲和力及其对锰离子(Mn2+)和钙离子(Ca2+)等金属离子的需求,至今已有约50年的研究历史。然而,金属离子结合与Con A的糖类结合活性之间的关系直到最近才得到详细研究。Brown等人(《生物化学》16卷,3883页(1977年))表明,Con A以两种构象状态的混合物形式存在:“锁定”形式和“未锁定”形式。蛋白质的未锁定形式与金属离子和糖类的结合较弱,并且是去金属化的Con A(脱辅基Con A,apo-Con A)在平衡状态下的主要构象。锁定形式每个单体结合两个金属离子,形成的复合物具有完全的糖类结合活性。Brown及其同事测量了未锁定形式向含有Mn2+和Ca2+的完全金属化锁定构象转变的动力学。他们还证明,单独的Mn2+可以与Con A形成锁定的三元复合物,并且快速去除离子会导致apo-Con A处于锁定构象的亚稳态形式,这种形式会缓慢地(在25℃下数小时)恢复为(主要是)未锁定构象。在有无金属离子的情况下形成两种构象的能力,使我们能够探索Con A中金属离子结合与构象转变之间的关系,这些关系是凝集素糖类结合活性的决定因素。基于未锁定的apo-Con A向完全金属化的锁定Con A转变的动力学以及X射线晶体学数据,Con A的两种构象之间的转变似乎涉及蛋白质主链中靠近两个金属离子结合位点之一的丙氨酸-天冬氨酸肽键的顺反异构化。转变的相对较大的活化能(约22千卡摩尔-1)导致构象之间的相互转化相对较慢(从几分钟到几天),而与金属离子和糖类的平衡则很快。因此,可以形成许多亚稳复合物,并研究两种构象之间的各种转变途径。我们已经鉴定并表征了含有Mn2+和糖类的Con A两种构象的二元、三元和四元复合物,并确定了它们所有的金属离子和糖类解离常数,以及它们之间构象转变的平衡和动力学值。(摘要截选至400字)