4.6 Review

Understanding and overcoming trade-offs between antibody affinity, specificity, stability and solubility

Journal

BIOCHEMICAL ENGINEERING JOURNAL
Volume 137, Issue -, Pages 365-374

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bej.2018.06.003

Keywords

mAb; Fab; Fc; CDR; Aggregation; Developability

Funding

  1. National Institutes of Health [R01GM104130]
  2. National Science Foundation (CBET) [1159943, 1605266]
  3. Albert M. Mattocks Chair
  4. Directorate For Engineering [1813963] Funding Source: National Science Foundation
  5. Directorate For Engineering
  6. Div Of Chem, Bioeng, Env, & Transp Sys [1605266] Funding Source: National Science Foundation
  7. Directorate For Engineering
  8. Div Of Chem, Bioeng, Env, & Transp Sys [1159943] Funding Source: National Science Foundation
  9. Div Of Chem, Bioeng, Env, & Transp Sys [1813963] Funding Source: National Science Foundation

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The widespread use of monoclonal antibodies for therapeutic applications has led to intense interest in optimizing several of their natural properties (affinity, specificity, stability, solubility and effector functions) as well as introducing non-natural activities (bispecificity and cytotoxicity mediated by conjugated drugs). A common challenge during antibody optimization is that improvements in one property (e.g., affinity) can lead to deficits in other properties (e.g., stability). Here we review recent advances in understanding trade-offs between different antibody properties, including affinity, specificity, stability and solubility. We also review new approaches for co-optimizing multiple antibody properties and discuss how these methods can be used to rapidly and systematically generate antibodies for a wide range of applications. (C) 2018 Elsevier B.V. All rights reserved.

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