Yu H, Soong N, Anderson W F
Gene Therapy Laboratories, Norris Cancer Center, University of Southern California School of Medicine, Los Angeles 90033, USA.
J Virol. 1995 Oct;69(10):6557-62. doi: 10.1128/JVI.69.10.6557-6562.1995.
A quantitative analysis of the binding kinetics of intact Moloney murine leukemia retrovirus (MoMuLV) particles with NIH 3T3 cells was performed with an immunofluorescence flow cytometry assay. The virus-cell binding equilibrium dissociation constant (KD), expressed in terms of virus particle concentration, was measured to be 8.5 (+/- 6.4) x 10(-12) M at 4 degrees C and was three- to sixfold lower at temperatures above 15 degrees C. The KD of virus binding is about 1,000-fold lower than the KD of purified MoMuLV envelope. The association rate constant was determined to be 2.5 (+/- 0.9) x 10(9) M-1 min-1 at 4 degrees C and was 5- to 10-fold higher at temperatures above 15 degrees C. The apparent dissociation rate constant at 4 degrees C was 1.1 (+/- 0.4) x 10(-3) min-1 and was doubled for every 10 degrees C increase in temperature over the range tested (15 to 37 degrees C).
采用免疫荧光流式细胞术对完整的莫洛尼鼠白血病病毒(MoMuLV)颗粒与NIH 3T3细胞的结合动力学进行了定量分析。以病毒颗粒浓度表示的病毒-细胞结合平衡解离常数(KD)在4℃时测得为8.5(±6.4)×10⁻¹² M,在15℃以上温度时低三至六倍。病毒结合的KD比纯化的MoMuLV包膜的KD低约1000倍。结合速率常数在4℃时测定为2.5(±0.9)×10⁹ M⁻¹ min⁻¹,在15℃以上温度时高5至10倍。4℃时的表观解离速率常数为1.1(±0.4)×10⁻³ min⁻¹,在所测试的温度范围(15至37℃)内,温度每升高10℃,该常数就增加一倍。