TY - JOUR
T1 - Accelerating high-concentration monoclonal antibody development with large-scale viscosity data and ensemble deep learning
AU - Kalejaye, Lateefat A.
AU - Chu, Jia Min
AU - Wu, I. En
AU - Amofah, Bismark
AU - Lee, Amber
AU - Hutchinson, Mark
AU - Chakiath, Chacko
AU - Dippel, Andrew
AU - Kaplan, Gilad
AU - Damschroder, Melissa
AU - Stanev, Valentin
AU - Pouryahya, Maryam
AU - Boroumand, Mehdi
AU - Caldwell, Jenna
AU - Hinton, Alison
AU - Kreitz, Madison
AU - Shah, Mitali
AU - Gallegos, Austin
AU - Mody, Neil
AU - Lai, Pin Kuang
N1 - Publisher Copyright:
© 2025 The Author(s). Published with license by Taylor & Francis Group, LLC.
PY - 2025
Y1 - 2025
N2 - 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.
AB - 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.
KW - Antibody viscosity
KW - ensemble deep learning
KW - high-concentration formulations
KW - monoclonal antibodies
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U2 - 10.1080/19420862.2025.2483944
DO - 10.1080/19420862.2025.2483944
M3 - Article
C2 - 40170162
AN - SCOPUS:105001870143
SN - 1942-0862
VL - 17
JO - mAbs
JF - mAbs
IS - 1
M1 - 2483944
ER -