单克隆抗体
粘度
概化理论
计算机科学
抗体
化学
人工智能
材料科学
数学
热力学
物理
生物
免疫学
统计
作者
Lateefat Kalejaye,Jia‐Min Chu,I-En Wu,Bismark Amofah,A. Lee,Mark R. Hutchinson,Chacko Chakiath,Andrew Dippel,Gilad Kaplan,Melissa Damschroder,Valentin Stanev,Maryam Pouryahya,Mohammad Ali Boroumand,J. Timothy Caldwell,Andrew Hinton,Madison Kreitz,Mitali Shah,Austin Gallegos,Neil Mody,Pin‐Kuang Lai
出处
期刊:mAbs
[Landes Bioscience]
日期:2025-04-01
卷期号:17 (1): 2483944-2483944
被引量:11
标识
DOI:10.1080/19420862.2025.2483944
摘要
Highly concentrated antibody solutions are necessary for developing subcutaneous injections but often exhibit high viscosities, posing challenges in antibody-drug development, manufacturing, and administration. Previous computational models were only limited to a few dozen data points for training, a bottleneck for generalizability. In this study, we measured the viscosity of a panel of 229 monoclonal antibodies (mAbs) to develop predictive models for high concentration mAb screening. We developed DeepViscosity, consisting of 102 ensemble artificial neural network models to classify low-viscosity (≤20 cP) and high-viscosity (>20 cP) mAbs at 150 mg/mL, using 30 features from a sequence-based DeepSP model. Two independent test sets, comprising 16 and 38 mAbs with known experimental viscosity, were used to assess DeepViscosity's generalizability. The model exhibited an accuracy of 87.5% and 89.5% on both test sets, respectively, surpassing other predictive methods. DeepViscosity will facilitate early-stage antibody development to select low-viscosity antibodies for improved manufacturability and formulation properties, critical for subcutaneous drug delivery. The webserver-based application can be freely accessed via https://devpred.onrender.com/DeepViscosity.
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