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结合曲线查看器:可视化蛋白质-配体结合和竞争结合的平衡和动力学。

Binding Curve Viewer: Visualizing the Equilibrium and Kinetics of Protein-Ligand Binding and Competitive Binding.

机构信息

Department of Clinical Laboratory, The Second Affiliated Hospital of Jiaxing University, Huancheng North Road 1518, Jiaxing, Zhejiang 314000, China.

The Key Laboratory, The Second Affiliated Hospital of Jiaxing University, Huancheng North Road 1518, Jiaxing, Zhejiang 314000, China.

出版信息

J Chem Inf Model. 2024 May 27;64(10):4180-4192. doi: 10.1021/acs.jcim.4c00130. Epub 2024 May 8.

Abstract

Understanding the thermodynamics and kinetics of the protein-ligand interaction is essential for biologists and pharmacologists. To visualize the equilibrium and kinetics of the binding reaction with 1:1 stoichiometry and no cooperativity, we obtained the exact relationship of the concentration of the protein-ligand complex and the time in the second-order binding process and numerically simulated the process of competitive binding. First, two common concerns in measuring protein-ligand interactions were focused on how to avoid the titration regime and how to establish the appropriate incubation time. Then, we gave examples of how the commonly used experimental conditions of [L] ≫ [P] and [I] ≫ [P] affected the estimation of the kinetic and thermodynamic properties. Theoretical inhibition curves were calculated, and the apparent IC and IC were estimated accordingly under predefined conditions. Using the estimated apparent IC, we compared the apparent and calculated by using the Cheng-Prusoff equation, Lin-Riggs equation, and Wang's group equation. We also applied our tools to simulate high-throughput screening and compare the results of real experiments. The visualization tool for simulating the saturation experiment, kinetic experiments of binding and competitive binding, and inhibition curve, "Binding Curve Viewer," is available at www.eplatton.net/binding-curve-viewer.

摘要

理解蛋白质 - 配体相互作用的热力学和动力学对于生物学家和药理学家来说至关重要。为了可视化具有 1:1 化学计量比且无协同性的结合反应的平衡和动力学,我们获得了二级结合过程中蛋白质 - 配体复合物浓度与时间的精确关系,并对竞争结合过程进行了数值模拟。首先,我们关注了在测量蛋白质 - 配体相互作用时两个常见的问题,即如何避免滴定范围以及如何确定适当的孵育时间。然后,我们给出了在 [L] ≫ [P] 和 [I] ≫ [P] 等常用实验条件下如何影响对动力学和热力学性质的估计的示例。计算了理论抑制曲线,并根据预设条件估算了表观 IC 和 IC。使用估算的表观 IC,我们比较了使用 Cheng-Prusoff 方程、Lin-Riggs 方程和 Wang 组方程计算得到的表观 和 。我们还应用我们的工具来模拟高通量筛选,并比较实际实验的结果。用于模拟饱和实验、结合动力学实验和竞争性结合实验以及抑制曲线的可视化工具“Binding Curve Viewer”可在 www.eplatton.net/binding-curve-viewer 获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a649/11134506/316b40aa2619/ci4c00130_0001.jpg

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