A homogeneous time-resolved fluorescence-based high-throughput screening for discovery of inhibitors of Nef-sdAb19 interaction.

The human immunodeficiency virus (HIV) protein negative factor (Nef) is important for AIDS pathogenesis. An anti-Nef single-domain antibody (sdAb19) derived from camelids has been previously generated and shown to effectively block the physiological functions of Nef in vitro and in vivo in nef-transgenic mice. However, sdAb19 must be ectopically expressed within the target cell to be able to exert its neutralizing effect on Nef, while the extra-cellular administration method turned out to be ineffective. This might suggest a default of the stability or/and deliverability of sdAb19. The identification of small molecule compounds capable of inhibiting the Nef-sdAb19 interaction and mimicking the neutralizing activity of sdAb19 in vivo would therefore be the means of circumventing the problem encountered with sdAb19. Here we describe the development of a high-throughput screening method combining the homogeneous time-resolved fluorescence (HTRF) and the microscale thermophoresis (MST) techniques for the identification of small-molecule compounds inhibiting the Nef-sdAb19 interaction by binding to Nef protein. Eight small-molecule compounds have been selected for their ability to significantly inhibit the Nef-sdAb19 interaction and to bind to Nef. These molecules could be further assessed for their potential of being the Nef-neutralizing agents in the future.

New method for the simultaneous analysis of types A and B trichothecenes by ultrahigh-performance liquid chromatography coupled with tandem mass spectrometry in potato tubers inoculated with Fusarium sulphureum.

A reliable and sensitive method for rapid simultaneous determination of two type A (T-2 and diacetoxyscirpenol) and two type B (3-acetyldeoxynivalenol and Fusarenon X) trichothecenes was developed and successfully applied for detecting trichothecenes in potato tubers by ultrahigh-performance liquid chromatography coupled with tandem mass spectrometry. The established method was further evaluated by determining the linearity (R ≥ 0.9995), recovery (113.28-77.97%), precision (relative standard deviation ≤ 5.89), and sensitivity (limit of detection, 0.002-0.005 µg/g; limit of quantitation, 0.005-0.015 µg/g). The method proved to be suitable for simultaneous determination of T-2, diacetoxyscirpenol, 3-acetyldeoxynivalenol, and Fusarenon X in potato tubers inoculated with Fusarium sulphureum . In addition, it was found that T-2, diacetoxyscirpenol, 3-acetyldeoxynivalenol, and Fusarenon X could be predominantly detected in the lesion, and the toxin could also be identified in tubers without any disease symptoms. The experimental results also indicated that the concentration of toxin in the susceptible cultivar (Longshu No. 3) was significantly higher than that in the resistant cultivar (Longshu No. 6).