A cell–cell interaction format for selection of high-affinity antibodies to membrane proteins
Author(s) -
Zhuo Yang,
Yue Wan,
Pingdong Tao,
Min Qiang,
Xue Dong,
Chih-Wei Lin,
Guang Yang,
Tianqing Zheng,
Richard A. Lerner
Publication year - 2019
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1908571116
Subject(s) - antibody , membrane protein , phage display , yeast , cell , cell membrane , biology , membrane , microbiology and biotechnology , computational biology , cell surface receptor , biochemistry , chemistry , immunology
Significance Antibodies are an important class of drugs. We developed a simple, easy-to-use method for antibody drug discovery targeting membrane proteins including gated ion channels and G protein-coupled receptors. While phage or yeast display provides a convenient tool for antibody screening, the development of therapeutic antibodies against membrane proteins still encounters bottlenecks, because it is usually difficult to purify membrane proteins in native conformation for selecting functional antibodies. To address this challenge, we designed a whole-cell screening platform based on yeast–mammalian cell interaction, which bypasses the step of membrane protein purification and enables the direct selection of antibodies against “difficult-to-purify membrane proteins” in native state.
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