Engineering High Affinity Protein-Protein Interactions Using a High-Throughput Microcapillary Array Platform

被引:12
作者
Lim, Sungwon [1 ]
Chen, Bob [1 ]
Kariolis, Mihalis S. [1 ]
Dimov, Ivan K. [2 ]
Baer, Thomas M. [3 ]
Cochran, Jennifer R. [1 ,4 ]
机构
[1] Stanford Univ, Dept Bioengn, 450 Serra Mall, Stanford, CA 94305 USA
[2] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, 450 Serra Mall, Stanford, CA 94305 USA
[3] Stanford Univ, Stanford Photon Res Ctr, 450 Serra Mall, Stanford, CA 94305 USA
[4] Stanford Univ, Chem Engn, 450 Serra Mall, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
YEAST SURFACE DISPLAY; POLYPEPTIDE LIBRARIES; DIRECTED EVOLUTION; HUMAN-ANTIBODIES; PCR;
D O I
10.1021/acschembio.6b00794
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Affinity maturation of protein protein interactions requires iterative rounds of protein library generation and high-throughput screening to identify variants that bind with increased affinity to a target of interest. We recently developed a multipurpose protein engineering platform, termed mu SCALE (Microcapillary Single Cell Analysis and Laser Extraction). This technology enables high-throughput screening of libraries of millions of cell-expressing protein variants based on their binding properties or functional activity. Here, we demonstrate the first use of the mu SCALE platform for affinity maturation of a protein protein binding, interaction. In this proof-of-concept study, we engineered an extracellular domain of the Axl receptor tyrosine kinase to bind tighter to its ligand Gas6. Within 2 weeks, two iterative rounds of library generation and screening resulted in engineered Axl variants with a 50-fold decrease in kinetic dissociation rate, highlighting the use of mu SCALE as a new tool for directed evolution.
引用
收藏
页码:336 / 341
页数:6
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