Institute for Analytical Instrumentation, Russian Academy of Sciences, Rizhskii pr. 26, St. Petersburg 190103, Russia.
J Theor Biol. 2010 May 7;264(1):37-44. doi: 10.1016/j.jtbi.2010.01.001. Epub 2010 Jan 11.
We present the results of our comprehensive study of precipitation pattern formation by interacting immunogenic proteins in a gel medium. Formation of immunoprecipitation patterns was studied both theoretically and experimentally. Based on a system of reaction-diffusion equations, continuous deterministic description provides a quantitative model of reaction kinetics. Discrete stochastic microscopic description was used to supplement the results of reaction-diffusion model by mimicking product aggregation that contributes to a deeper understanding of the mechanism that governs the phenomenon. Our studies have shown that the mechanism of immunoprecipitation pattern formation is specific for protein precipitation and differs from such mechanisms for any inorganic or biological substances. By microscopic examination, we demonstrated that immunoprecipitation patterns can have a microstructure. We found that the microscopic structure of immunoprecipitation patterns results from multicomponent composition of antiserum.
我们展示了在凝胶介质中相互作用的免疫原性蛋白质形成沉淀模式的综合研究结果。沉淀模式的形成在理论和实验上都进行了研究。基于反应-扩散方程系统,连续确定性描述为反应动力学提供了定量模型。离散随机微观描述通过模拟产物聚集来补充反应-扩散模型的结果,这有助于更深入地了解控制该现象的机制。我们的研究表明,免疫沉淀模式形成的机制是针对蛋白质沉淀的,与任何无机或生物物质的沉淀机制不同。通过微观检查,我们证明了免疫沉淀模式可以具有微观结构。我们发现免疫沉淀模式的微观结构是由抗血清的多组分组成造成的。