An ultrasensitive assay for the detection of Pb(II) has been developed using whispering gallery mode (WGM) sensing. In this technique a photonic microcavity was decorated with glutathione (GSH)-modified gold nanoparticles (Au NPs). The resonator was functionalized using an aminosilane to promote adhesion of the GSH-modified NPs creating a highly sensitive sensor specific to Pb(II). Upon introduction of Pb(II) solutions via a fluidic cell, Pb(II) ions bind to the GSH-Au NP complex and induce a shift of the resonant wavelength. Using this detection strategy we show that we are able to detect Pb(II) concentrations down to 0.05 nM in the presence of alkaline and heavy metal interferences such as Mg(II), Mn(II), Ca(II), Ni(II), Cd(II), Cr(II), Fe(II), and Hg(II). The signal was found to be proportional to the Pb(II) concentration within the range of 2.40-48.26 nM and was found to have an association constant of 2.15 × 10(5) M(-1) s(-1). The sensitivity obtained shows unparalleled advantages over currently available technology and satisfies the exposure thresholds set out by world organizations such as International Agency for Research on Cancer (IARC) and the Environmental Protection Agency (EPA). We believe that this sensor has the potential to be made portable for applications in environmental monitoring and in-field applications.

No abstract

p53 is an anti-tumor protein that plays an important role in apoptosis, preserving genomic stability and preventing angiogenesis, and it has been implicated in a large number of human cancers. For this reason it is an interesting target for both fundamental studies, such as the mechanism of interaction with DNA, and applications in biosensing. Here, we report a comprehensive study of label-free, full length p53 (flp53) and its interaction with engineered double-stranded DNA in vitro, at the single-molecule level, using Atomic Force Microscopy (AFM) imaging and solid-state nanopore sensing. AFM data show that dimeric and tetrameric p53 bind to the DNA in a sequence-specific manner, confirming previously reported relative binding affinities. The statistical significance is tested using both the Grubbs test and stochastic simulations. For the first time, ultra-low noise solidstate nanopore sensors are employed for the successful differentiation between bare DNA and p53/DNA complexes. Furthermore, translocation statistics reflect the binding affinities of different DNA sequences, in accordance with AFM data. Our results thus highlight the potential of solid-state nanopore sensors for single-molecule biosensing, especially when labelling is either not possible or at least not a viable option.

No abstract

Single-crystal X-ray diffraction photographs have revealed eight polymorphs of cronstedtite, and the structures of four of them, with space groups P31m, P63cm, P31 and R3, have been determined.All the structures, assumed to have the idealized composition (Fe2+)3(Fe3+Si)Od(OH)s, are formed from kaolin-type layers, the principal differences being in the manner in which these layers are stacked together. Distortion of the Fe, Si-O, OH tetrahedra is related to the cation-anion attraction either within a layer or between adjacent layers.