Phage-display technology--finding a needle in a vast molecular haystack.

Screening of phage-displayed libraries of proteins and peptides has, for nearly a decade, proven to be a highly effective method for finding much needed 'needles' in a vast molecular 'haystack'. Over the past year, it has been used to solve an increasing diversity of problems, including identification of binding motifs for much smaller targets and the use of novel screening methods to identify chemical activities.

DNA damage, micronucleus formation, and cell death from 125I decays in DNA.

CHO cells were pulse-labeled with 125I-iododeoxyuridine, harvested 30 min or 5 h after labeling, and stored at -196 degrees C for accumulation of 125I decays. The 30- min groups yielded low-LET survival curves (large shoulder, D0 136 decays/cell); 5-h groups showed a high-LET pattern of cell killing (no shoulder, D0 45 decay/cell). Surprisingly, the shift in 125I action was abolished in cells exposed to HAT medium; both 30-min and 5-h cell groups exhibited high-LET-type killing (no shoulder, D0 52 decays/cell).