Yeast display biopanning identifies human antibodies targeting glioblastoma stem-like cells

被引:14
作者
Zorniak, Michael [1 ,2 ]
Clark, Paul A. [2 ]
Umlauf, Benjamin J. [3 ]
Cho, Yongku [3 ]
Shusta, Eric V. [3 ,4 ]
Kuo, John S. [1 ,2 ,4 ]
机构
[1] Univ Wisconsin, Neurosci Training Program, Sch Med & Publ Hlth, Madison, WI 53792 USA
[2] Univ Wisconsin, Dept Neurol Surg, Sch Med & Publ Hlth, Madison, WI 53792 USA
[3] Univ Wisconsin, Dept Chem & Biol Engn, Sch Med & Publ Hlth, Madison, WI 53792 USA
[4] Univ Wisconsin, Carbone Canc Ctr, Sch Med & Publ Hlth, Madison, WI 53792 USA
关键词
BLOOD-BRAIN-BARRIER; SACCHAROMYCES-CEREVISIAE; DIRECTED EVOLUTION; SURFACE DISPLAY; INITIATING CELLS; T-CELLS; CANCER; EXPRESSION; PROTEINS; AFFINITY;
D O I
10.1038/s41598-017-16066-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Glioblastoma stem-like cells (GSC) are hypothesized to evade current therapies and cause tumor recurrence, contributing to poor patient survival. Existing cell surface markers for GSC are developed from embryonic or neural stem cell systems; however, currently available GSC markers are suboptimal in sensitivity and specificity. We hypothesized that the GSC cell surface proteome could be mined with a yeast display antibody library to reveal novel immunophenotypes. We isolated an extensive collection of antibodies that were differentially selective for GSC. A single domain antibody VH-9.7 showed selectivity for five distinct patient-derived GSC lines and visualized orthotopic GBM xenografts in vivo after conjugation with a near-infrared dye. These findings demonstrate a previously unexplored high-throughput strategy for GSC-selective antibody discovery, to aid in GSC isolation, diagnostic imaging, and therapeutic targeting.
引用
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页数:12
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