High affinity ligands from in vitro selection:: Complex targets

被引:269
作者
Morris, KN [1 ]
Jensen, KB
Julin, CM
Weil, M
Gold, L
机构
[1] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
[2] NeXstar Pharmaceut Inc, Boulder, CO 80301 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Radiat Oncol, Denver, CO 80262 USA
关键词
D O I
10.1073/pnas.95.6.2902
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
Human red blood cell membranes were used as a model system to determine if the systematic evolution of ligands by exponential enrichment (SELEX) methodology, an in vitro protocol for isolating high-affinity oligonucleotides that bind specifically to virtually any single protein, could be used with a complex mixture of potential targets, Ligands to multiple targets were generated simultaneously during the selection process, and the binding affinities of these ligands for their targets are comparable to those found in similar experiments against pure targets, A secondary selection scheme, deconvolution-SELEX, facilitates rapid isolation of the ligands to targets of special interest within the mixture, SELEX provides high-affinity compounds for multiple targets in a mixture and might allow a means for dissecting complex biological systems.
引用
收藏
页码:2902 / 2907
页数:6
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