Computer-based engineering of thermostabilized antibody fragments
- Authors
- Lee, Jiwon; Der, Bryan S.; Karamitros, Christos S.; Li, Wenzong; Marshall, Nicholas M.; Lungu, Oana I.; Miklos, Aleksandr E.; Xu, Jianqing; Kang, Tae Hyun; Lee, Chang-Han; Tan, Bing; Hughes, Randall A.; Jung, Sang Taek; Ippolito, Gregory C.; Gray, Jeffrey J.; Zhang, Yan; Kuhlman, Brian; Georgiou, George; Ellington, Andrew D.
- Issue Date
- 3월-2020
- Publisher
- WILEY
- Keywords
- antibody engineering; thermostable antibodies; Rosetta; scAb; scFv
- Citation
- AICHE JOURNAL, v.66, no.3
- Indexed
- SCIE
SCOPUS
- Journal Title
- AICHE JOURNAL
- Volume
- 66
- Number
- 3
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/57593
- DOI
- 10.1002/aic.16864
- ISSN
- 0001-1541
- Abstract
- We used the molecular modeling program Rosetta to identify clusters of amino acid substitutions in antibody fragments (scFvs and scAbs) that improve global protein stability and resistance to thermal deactivation. Using this methodology, we increased the melting temperature (T-m) and resistance to heat treatment of an antibody fragment that binds to the Clostridium botulinum hemagglutinin protein (anti-HA33). Two designed antibody fragment variants with two amino acid replacement clusters, designed to stabilize local regions, were shown to have both higher T-m compared to the parental scFv and importantly to retain full antigen binding activity after 2 hr of incubation at 70 degrees C. The crystal structure of one thermostabilized scFv variants was solved at 1.6 angstrom and shown to be in close agreement with the RosettaAntibody model prediction.
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Collections - Graduate School > Department of Biomedical Sciences > 1. Journal Articles
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