The emergence of antibiotic-resistant bacteria is a major threat to world-wide public health. Functionalized nanoparticles could offer novel strategies in this post-antibiotic era. In this study, we developed nanocomposites of silver nanoparticles decorated with graphene quantum dots (Ag-GQDs) using pulsed laser synthesis. The nanocomposites were PEGylated, which increases their biocompatibility and solubility in aqueous solutions. The HR-TEM micrographs of bare GQDs show that their size is in the range of 1.6–4nm, and the lattice spacing is 0.214nm, which corresponds to the (100) lattice fringes of graphene. The antibacterial activity of Ag-GQDs was evaluated and compared to that of bare GQDs and commercial silver nanoparticles (Ag-NPs) against both Gram-negative and Gram-positive bacteria, using Pseudomonas aeruginosa and Staphylococcus aureus as model bacteria, respectively. Concentration values of 25 and 50μg/mL are required for Ag-GQDs to inhibit the growth of S. aureus and P. aeruginosa bacteria, respectively. The fractional inhibitory concentration (FIC) index is below 0.5 indicating that there is a synergistic effect between Ag-NPs and GQDs. Kirby–Bauer tests showed that Ag-GQDs inhibit P. aeruginosa and S. aureus, in contrast to bare GQDs and Ag-NPs alone. Cell viability of normal mammalian cells treated with Ag-GQDs showed that cell viability is maintained at 100% for cells incubated with Ag-GQDs. The decoration of Ag-NPs with GQDs minimizes their cytotoxicity in mammalian cells and increases their biocompatibility. Ag-GQDs have potential applications in the fabrication of antibacterial coatings, self-sterile textiles, and personal care products

Telomerase overexpression has been associated directly with cancer, and the enzyme itself is recognized within the scientific community as a cancer biomarker. BIDEA’s biosensing strip (BBS) is an innovative technology capable of detecting the presence of telomerase activity (TA) using electrochemical impedance spectroscopy (EIS). This BBS is an interdigital gold (GID) electrode array similar in size and handling to a portable glucose sensor. For the detection of the biomarker, BBS was modified by the immobilization of a telomere-like single strand DNA (ssDNA) on its surface. The sensor was exposed to telomerase-positive extract from commercially available cancer cells, and the EIS spectra were measured. Telomerase recognizes the sequence of this immobilized ssDNA probe on the BBS, and the reverse transcription process that occurs in cancer cells is replicated, resulting in the ssDNA probe elongation. This surface process caused by the presence of TA generates changes in the capacitive process on the electrode array microchip surface, which is followed by EIS as the sensing tool and correlated with the presence of cancer cells. The telomerases’ total cell extraction protocol results demonstrate significant changes in the charge-transfer resistance (R_ct) change rate after exposure to telomerase-positive extract with a detection limit of 2.94 × 10⁴ cells/mL. Finally, a preliminary study with a small set of “blind” uterine biopsy samples suggests the feasibility of using the changes in the R_ct magnitude change rate (Δ(ΔR_ct/R_cti)/Δt) to distinguish positive from negative endometrial adenocarcinoma samples by the presence or absence of TA.

Thirty percent of all mutations causing human disease generate mRNAs with premature termination codons (PTCs). Recognition and degradation of these PTC-containing mRNAs is carried out by the mechanism known as nonsense-mediated mRNA decay (NMD). Upf2 is a scaffold protein known to be a central component of the NMD surveillance pathway. It harbors three middle domains of eukaryotic initiation factor 4G (mIF4G-1, mIF4G-2, mIF4G-3) in its N-terminal region that are potentially important in regulating the surveillance pathway. In this study, we defined regions within the mIF4G-1 and mIF4G-2 that are required for proper function of Upf2p in NMD and translation termination in Saccharomyces cerevisiae. In addition, we narrowed down the activity of these regions to an aspartic acid (D59) in mIF4G-1 that is important for NMD activity and translation termination accuracy. Taken together, these studies suggest that inherently charged residues within mIF4G-1 of Upf2p play a role in the regulation of the NMD surveillance mechanism in S. cerevisiae.

Thirty percent of all mutations causing human diseases generate mRNAs with premature termination codons (PTCs). Recognition and degradation of these PTC-containing mRNAs is carried out by the mechanism known as nonsense-mediated mRNA decay (NMD). Upf2 is a scaffold protein known to be a central component of the NMD surveillance pathway. It harbors three middle domain of eukaryotic initiation factor 4G (mIF4G) domains in its N-terminal potentially important in regulating the surveillance pathway. In this study, we defined regions within the mIF4G-1 and mIF4G-2 that are required for proper function of NMD and translation termination in Saccharomyces cerevisiae Upf2. In addition, we narrowed down the activity of these regions to an aspartic acid (D59) in mIF4G-1 which is important for NMD activity and translation termination accuracy. Taken together, these studies suggest that inherent charged residues within mIF4G-1 of Upf2 play a role in the regulation of the NMD surveillance mechanism in S. cerevisiae .