rAbDesFlow: a novel workflow for computational recombinant antibody design for healthcare engineering.
Sowmya Ramaswamy KrishnanDivya SharmaYasin NazeerMayilvahanan BoseThangarajan RajkumarGuhan JayaramanNarayanan MadaboosiM Michael GromihaPublished in: Antibody therapeutics (2024)
Recombinant antibodies (rAbs) have emerged as a promising solution to tackle antigen specificity, enhancement of immunogenic potential and versatile functionalization to treat human diseases. The development of single chain variable fragments has helped accelerate treatment in cancers and viral infections, due to their favorable pharmacokinetics and human compatibility. However, designing rAbs is traditionally viewed as a genetic engineering problem, with phage display and cell free systems playing a major role in sequence selection for gene synthesis. The process of antibody engineering involves complex and time-consuming laboratory techniques, which demand substantial resources and expertise. The success rate of obtaining desired antibody candidates through experimental approaches can be modest, necessitating iterative cycles of selection and optimization. With ongoing advancements in technology, in silico design of diverse antibody libraries, screening and identification of potential candidates for in vitro validation can be accelerated. To meet this need, we have developed rAbDesFlow, a unified computational workflow for recombinant antibody engineering with open-source programs and tools for ease of implementation. The workflow encompasses five computational modules to perform antigen selection, antibody library generation, antigen and antibody structure modeling, antigen-antibody interaction modeling, structure analysis, and consensus ranking of potential antibody sequences for synthesis and experimental validation. The proposed workflow has been demonstrated through design of rAbs for the ovarian cancer antigen Mucin-16 (CA-125). This approach can serve as a blueprint for designing similar engineered molecules targeting other biomarkers, allowing for a simplified adaptation to different cancer types or disease-specific antigens.
Keyphrases
- cell free
- healthcare
- endothelial cells
- primary care
- public health
- squamous cell carcinoma
- magnetic resonance imaging
- electronic health record
- genome wide
- gene expression
- magnetic resonance
- drug delivery
- papillary thyroid
- young adults
- dna methylation
- cancer therapy
- risk assessment
- cystic fibrosis
- induced pluripotent stem cells
- genome wide identification