The use of display technologies to identify small molecule receptors from proteome libraries would provide a significant advantage in drug discovery. We have used mRNA display to select, based on affinity, proteins that bind to a drug of interest. A library of mRNA-protein fusion molecules was constructed from human liver, kidney, and bone marrow transcripts and selected using an immobilized FK506-biotin conjugate. Three rounds of selection produced full-length FKBP12 (FK506 binding protein 12 kDa) as the dominant clone. An analogous method was also used to map the minimal drug binding domain within FKBP12. Using this approach, it is anticipated that mRNA display could eventually play a key role in the discovery and characterization of new drug receptor interactions.

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Antibiotics can accumulate in soils via different ways, which may pose serious threat to ecological environment of soil and quality of agricultural products. In this study, the occurrence of 12 antibiotics including four sulfonamides (SAs), four tetracyclines (TETs) and four fluoroquinolones (FQs) was investigated in soils from four sampling sites of Kenya (Mai Mahiu, Narok, Mount Suswa Conservancy, and Juja), Africa. The soils in suburban area of Narok had the highest average concentrations of total 12 antibiotics with an average value of 43.64 μg kg(-1) dw (dry weight), followed by Mai Mahiu (26.70 μg kg(-1) dw), Juja (24.41 μg kg(-1) dw) and Mount Suswa Conservancy (12.21 μg kg(-1) dw). Sulfamethoxazole, sulfamethazine, oxytetracycline, and enrofloxacin were identified as the main antibiotics polluted in soils. Total organic carbon may influence the distribution of SAs in Narok and FQs in Juja. Ecological risk analysis based on the risk quotient showed that SAs detected in soils have higher risk compared to TETs and FQs.

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