Stutz C Christopher, Georgieva Julia V, Shusta Eric V
Dept. of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, WI 53706.
AIChE J. 2018 Dec;64(12):4229-4236. doi: 10.1002/aic.16360. Epub 2018 Aug 22.
Antibodies that target the blood-brain barrier (BBB) are of particular interest for the treatment of neurological diseases. Here, we screened a phage display single-chain antibody (scFv) library by brain perfusion in an attempt to isolate scFv that target the rat BBB. After four rounds of screening, the resulting antibody pool remained highly complex and discrete clonal sampling did not identify any scFvs capable of binding to the rat BBB. Thus, the heavy chain CDR3 in the resulting pools was subjected to NGS, and the resulting data was used to identify 12 scFv clones that were of high abundance and/or enriched from round 3 to 4, signifying potential hits. Of these, two scFv, denoted scFv 4 and scFv 40, were identified that bound the rat BBB. Neither of these scFvs was identified by discrete sampling, motivating NGS as a tool to identify lead antibodies from complex screens.
靶向血脑屏障(BBB)的抗体在神经疾病治疗中具有特别的意义。在此,我们通过脑灌注筛选了一个噬菌体展示单链抗体(scFv)文库,试图分离出靶向大鼠血脑屏障的scFv。经过四轮筛选后,所得抗体库仍然高度复杂,离散克隆取样未鉴定出任何能够与大鼠血脑屏障结合的scFv。因此,对所得文库中的重链互补决定区3(CDR3)进行了二代测序(NGS),所得数据用于鉴定12个高丰度和/或从第3轮至第4轮富集的scFv克隆,这些克隆代表潜在的命中抗体。其中,鉴定出两个与大鼠血脑屏障结合的scFv,分别命名为scFv 4和scFv 40。离散取样未鉴定出这些scFv中的任何一个,这表明NGS可作为从复杂筛选中鉴定先导抗体的工具。