TY - JOUR
T1 - Microfluidic chip-based online screening coupled to mass spectrometry: Identification of inhibitors of thrombin and factor Xa
AU - Iyer, J.
AU - Ötvös, R.A.
AU - Kool, J.
AU - Kini, R.M.
PY - 2016/2
Y1 - 2016/2
N2 - Thrombin and factor Xa (FXa) are critical enzymes of the blood coagulation cascade and are excellent targets of anticoagulant agents. Natural sources present an array of anticoagulants that can be developed as antithrombotic drugs. High-resolution, online screening techniques have been developed for the identification of drug leads from complex mixtures. In this study, we have developed and optimized a microfluidic online screening technique coupled to nano–liquid chromatography (LC) and in parallel with a mass spectrometer for the identification of thrombin and FXa inhibitors in mixtures. Inhibitors eluting from the nano-LC were split postcolumn in a 1:1 ratio; half was fed into a mass spectrometer (where its mass is detected), and the other half was fed into a microfluidic chip (which acts as a microreactor for the online assays). With our platform, thrombin and FXa inhibitors were detected in the assay in parallel with their mass identification. These methods are suitable for the identification of inhibitors from sample amounts as low as sub-microliter volumes.
AB - Thrombin and factor Xa (FXa) are critical enzymes of the blood coagulation cascade and are excellent targets of anticoagulant agents. Natural sources present an array of anticoagulants that can be developed as antithrombotic drugs. High-resolution, online screening techniques have been developed for the identification of drug leads from complex mixtures. In this study, we have developed and optimized a microfluidic online screening technique coupled to nano–liquid chromatography (LC) and in parallel with a mass spectrometer for the identification of thrombin and FXa inhibitors in mixtures. Inhibitors eluting from the nano-LC were split postcolumn in a 1:1 ratio; half was fed into a mass spectrometer (where its mass is detected), and the other half was fed into a microfluidic chip (which acts as a microreactor for the online assays). With our platform, thrombin and FXa inhibitors were detected in the assay in parallel with their mass identification. These methods are suitable for the identification of inhibitors from sample amounts as low as sub-microliter volumes.
UR - https://www.scopus.com/pages/publications/84954542313
UR - https://www.scopus.com/inward/citedby.url?scp=84954542313&partnerID=8YFLogxK
U2 - 10.1177/1087057115602648
DO - 10.1177/1087057115602648
M3 - Article
SN - 1087-0571
VL - 21
SP - 212
EP - 220
JO - Journal of Biomolecular Screening
JF - Journal of Biomolecular Screening
IS - 2
ER -