Dudley M A, Henkens R W, Rowlands D T
Proc Natl Acad Sci U S A. 1970 Jan;65(1):88-95. doi: 10.1073/pnas.65.1.88.
The neutralization of bacteriophage f2 by intact gammaG-immunoglobulin or fragments is first order with respect to both bacteriophage and antibody. Minimum values for the rate constants are of the order of 10(7)M(-1) sec(-1). The temperature dependence of the rates corresponds to the activation parameters: DeltaHdouble dagger = 6.7 kcal mole(-1) and DeltaSdouble dagger = -4 cal deg(-1) mole(-1) (gammaG-immunoglobulin); DeltaHdouble dagger = 8.0 kcal mole(-1) and DeltaSdouble dagger = -0.9 cal deg(-1) mole(-1) (5S pepsin fragment); and DeltaHdouble dagger = 13.3 kcal mole(-1) and DeltaSdouble dagger = 12 cal deg(-1) mole(-1) (3.5S fragment). The kinetic observations are consistent with the view that the binding of a single antibody molecule can bring about phage neutralization. There are two ways in which a single antibody molecule can affect neutralization: (1) binding at or near some critical site on the phage may block its function, (2) binding may disturb the general architectural design of the protein shell of the phage. Although the rate of neutralization varied directly with antibody size, consideration of the activation parameters speaks against the dependence of neutralization on simple steric factors. Addition of antibodies directed against rabbit gammaG-immunoglobulin or the 5S pepsin fragment caused approximately a threefold neutralization enhancement. This enhancement may result from the detection of a class of infectious bacteriophage antibody complexes.
完整的γG-免疫球蛋白或其片段对噬菌体f2的中和作用,相对于噬菌体和抗体均呈一级反应。速率常数的最小值约为10(7)M(-1)秒(-1)。反应速率的温度依赖性符合以下活化参数:ΔH‡ = 6.7千卡/摩尔,ΔS‡ = -4卡/度·摩尔(γG-免疫球蛋白);ΔH‡ = 8.0千卡/摩尔,ΔS‡ = -0.9卡/度·摩尔(5S胃蛋白酶片段);以及ΔH‡ = 13.3千卡/摩尔,ΔS‡ = 12卡/度·摩尔(3.5S片段)。动力学观察结果与单个抗体分子的结合可导致噬菌体中和的观点一致。单个抗体分子影响中和作用有两种方式:(1) 在噬菌体上的某个关键位点或其附近结合可能会阻断其功能,(2) 结合可能会扰乱噬菌体蛋白质外壳的整体结构设计。尽管中和速率与抗体大小直接相关,但对活化参数的考量表明中和作用并非依赖于简单的空间因素。添加针对兔γG-免疫球蛋白或5S胃蛋白酶片段的抗体可使中和作用增强约三倍。这种增强可能是由于检测到一类感染性噬菌体-抗体复合物所致。