Gorshkova Inna I, Svitel Juraj, Razjouyan Faezeh, Schuck Peter
Dynamics of Macromolecular Assembly, Laboratory of Bioengineering and Physical Science, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, Maryland 20892, USA.
Langmuir. 2008 Oct 21;24(20):11577-86. doi: 10.1021/la801186w. Epub 2008 Sep 24.
Once a homogeneous ensemble of a protein ligand is taken from solution and immobilized to a surface, for many reasons the resulting ensemble of surface binding sites to soluble analytes may be heterogeneous. For example, this can be due to the intrinsic surface roughness causing variations in the local microenvironment, nonuniform density distribution of polymeric linkers, or nonuniform chemical attachment producing different protein orientations and conformations. We previously described a computational method for determining the distribution of affinity and rate constants of surface sites from analysis of experimental surface binding data. It fully exploits the high signal/noise ratio and reproducibility provided by optical biosensor technology, such as surface plasmon resonance. Since the computational analysis is ill conditioned, the previous approach used a regularization strategy assuming a priori all binding parameters to be equally likely, resulting in the broadest possible parameter distribution consistent with the experimental data. We now extended this method in a Bayesian approach to incorporate the opposite assumption, i.e., that the surface sites a priori are expected to be uniform (as one would expect in free solution). This results in a distribution of binding parameters as close to monodispersity as possible given the experimental data. Using several model protein systems immobilized on a carboxymethyl dextran surface and probed with surface plasmon resonance, we show microheterogeneity of the surface sites in addition to broad populations of significantly altered affinity. The distributions obtained are highly reproducible. Immobilization conditions and the total surface density of immobilized sites can have a substantial impact on the functional distribution of the binding sites.
一旦从溶液中获取蛋白质配体的均匀集合并将其固定在表面上,由于多种原因,所得的与可溶性分析物结合的表面位点集合可能是异质的。例如,这可能是由于固有表面粗糙度导致局部微环境变化、聚合物连接体的密度分布不均匀,或化学连接不均匀导致蛋白质取向和构象不同。我们之前描述了一种计算方法,通过分析实验表面结合数据来确定表面位点的亲和力和速率常数分布。它充分利用了光学生物传感器技术(如表面等离子体共振)提供的高信噪比和可重复性。由于计算分析条件不佳,之前的方法采用了一种正则化策略,假设所有结合参数先验地具有同等可能性,从而得到与实验数据一致的最宽泛的参数分布。我们现在将这种方法扩展为贝叶斯方法,以纳入相反的假设,即表面位点先验地预期是均匀的(如同在自由溶液中所预期的那样)。这导致在给定实验数据的情况下,结合参数分布尽可能接近单分散性。使用固定在羧甲基葡聚糖表面并通过表面等离子体共振进行探测的几种模型蛋白质系统,我们除了观察到大量亲和力显著改变的群体外,还展示了表面位点的微观异质性。所获得的分布具有高度可重复性。固定条件和固定位点的总表面密度会对结合位点的功能分布产生重大影响。