scholarly journals High-throughput sequencing allows the identification of binding molecules isolated from DNA-encoded chemical libraries

2008 ◽  
Vol 105 (46) ◽  
pp. 17670-17675 ◽  
Author(s):  
Luca Mannocci ◽  
Yixin Zhang ◽  
Jörg Scheuermann ◽  
Markus Leimbacher ◽  
Gianluca De Bellis ◽  
...  

DNA encoding facilitates the construction and screening of large chemical libraries. Here, we describe general strategies for the stepwise coupling of coding DNA fragments to nascent organic molecules throughout individual reaction steps as well as the first implementation of high-throughput sequencing for the identification and relative quantification of the library members. The methodology was exemplified in the construction of a DNA-encoded chemical library containing 4,000 compounds and in the discovery of binders to streptavidin, matrix metalloproteinase 3, and polyclonal human IgG.

2010 ◽  
Vol 20 (14) ◽  
pp. 4188-4192 ◽  
Author(s):  
Fabian Buller ◽  
Martina Steiner ◽  
Jörg Scheuermann ◽  
Luca Mannocci ◽  
Ina Nissen ◽  
...  

2014 ◽  
Vol 20 (2) ◽  
pp. 202-211 ◽  
Author(s):  
Dae Song Jang ◽  
Narsimha R. Penthala ◽  
Eugene O. Apostolov ◽  
Xiaoying Wang ◽  
Tariq Fahmi ◽  
...  

Deoxyribonuclease I (DNase I), the most active and abundant apoptotic endonuclease in mammals, is known to mediate toxic, hypoxic, and radiation injuries to the cell. Neither inhibitors of DNase I nor high-throughput methods for screening of high-volume chemical libraries in search of DNase I inhibitors are, however, available. To overcome this problem, we developed a high-throughput DNase I assay. The assay is optimized for a 96-well plate format and based on the increase of fluorescence intensity when fluorophore-labeled oligonucleotide is degraded by the DNase. The assay is highly sensitive to DNase I compared to other endonucleases, reliable (Z’ ≥ 0.5), and operationally simple, and it has low operator, intraassay, and interassay variability. The assay was used to screen a chemical library, and several potential DNase I inhibitors were identified. After comparison, 2 hit compounds were selected and shown to protect against cisplatin-induced kidney cell death in vitro. This assay will be suitable for identifying inhibitors of DNase I and, potentially, other endonucleases.


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