A novel enzyme-free signal amplification-based assay for highly sensitive in situ fluorescence imaging and detection of intracellular telomerase activity was developed by using a gold nanoflare probe-triggered mimic-hybridization chain reaction (mimic-HCR) coupled with a graphene oxide (GO) surface-anchored fluorescence signal readout pathway. The nanoflare probe consists of gold nanoparticles (AuNPs) functionalized with a dense shell of nucleic acid sequences by Au-S bond formation. The nucleic acid sequence is composed of three segments: a long thiol-labeled sequence (HS-DNA) and two short sequences (a telomerase primer sequence, "Primer-DNA", and an FAM-terminated reporter sequence, "Flare-DNA"), both of which are complementary to HS-DNA. The mimic-HCR system is formed by two FAM-modified hairpin sequences that are adsorbed on GO. Upon endocytosis of the AuNP/GO combinatorial probe, the Primer-DNA can be extended by intracellular telomerase at its 3' end to produce the telomeric repeated sequence, which leads to inner chain substitution and not only releases the Flare-DNA to turn on the fluorescence of FAM but also initiates the subsequent signal amplification and enrichment for the mimic-HCR system anchored on GO. The proposed approach can sensitively detect telomerase activity in living cells, distinguish normal cells from cancer cells, and monitor the change in telomerase activity in response to a telomerase inhibitor.

Shape memory epoxy polymer (SMEP) composite specimens with different graphene oxide (GO) contents were manufactured to study the effects of GO mass fractions on epoxy polymer composites. While ensuring the shape memory effect of SMEP, the addition of GO also remarkably strengthened the mechanical performance of the polymers. Analyses of the epoxy polymer composites’ thermal, mechanical, and shape memory performance were conducted through carrying out dynamic mechanical analysis (DMA), thermogravimetric analysis (TGA), and static tensile, three-point bending, impact, and shape memory tests. Moreover, the tensile fracture, bending fracture, and impact fracture interfaces of epoxy resin composites were examined with scanning electron microscopy. The final test results indicated that when the GO content was 0.8 wt %, SMEP composites had good shape memory performance and optimum thermal and mechanical performance.

Phosphorylation, one of the most important post-translational modifications of protein, plays a crucial role in a large number of biological processes. Large-scale identification of protein phosphorylation by mass spectrometry is still a challenging task because of the low abundance of phosphopeptides and sub-stoichiometry of phosphorylation. In this work, a novel strategy based on the specific affinity of zirconium arsenate to the phosphate group has been developed for the effective enrichment of phosphopeptides. Zirconium arsenate-modified magnetic nanoparticles (ZrAs-Fe(3)O(4)@SiO(2)) were prepared by covalent immobilization of zirconium arsenate on Fe(3)O(4)@SiO(2) magnetic nanoparticles under mild conditions, and characterized by transmission electron microscope (TEM), Fourier transform infrared (FT-IR) spectroscopy, energy dispersive X-ray spectroscopy (EDX) and vibrating sample magnetometer (VSM). The prepared ZrAs-Fe(3)O(4)@SiO(2) was applied for the selective enrichment of phosphopeptides from the digestion mixture of phosphoproteins and bovine serum albumin (BSA). Our results demonstrated that the ZrAs-Fe(3)O(4)@SiO(2) magnetic nanoparticles possess higher selectivity for phosphopeptides and better capture capability towards multiply-phosphorylated peptides than commercial zirconium dioxide (ZrO(2)), which has been widely employed for the enrichment of phosphopeptides. In addition, endogenous phosphopeptides from human serum can be effectively captured by ZrAs-Fe(3)O(4)@SiO(2) magnetic nanoparticles. It is the first report, to the best of our knowledge, in which the zirconium arsenate-modified magnetic nanoparticles were successfully applied to the enrichment of phosphopeptides, which offers the potential application of this new material in phosphoproteomics study.

A magnetite/oxidized carbon nanotube composite, Fe(3)O(4)@SiO(2)/OCNT, was fabricated in a simple way, and it was successfully used as a magnetic solid-phase extraction sorbent and a significant matrix of the matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) for the detection of benzo[a]pyrene (BaP).

Trans-l,4-polyisoprene (TPI) shape memory polymer composites with different chopped carbon fiber mass fractions were prepared to study the effects of different chopped carbon fiber mass fractions and temperatures on the TPI shape memory polymer composites in this paper. While guaranteeing the shape memory effect of TPI shape memory polymers, the carbon fiber fillers also significantly enhanced the mechanical properties of the polymers. The thermodynamic properties and shape memory properties of TPI shape memory polymers were studied by a differential scanning calorimeter (DSC) test, dynamic mechanical analysis (DMA) test, thermal conductivity test, static tensile test, mechanical cycle test, thermodynamic cycling test and shape memory test. Furthermore, the tensile fracture interface of TPI shape memory polymer composites was analyzed by scanning electron microscopy. The experimental results show that when the chopped carbon mass fraction fiber is 8%, TPI shape memory polymers have good shape memory properties and the best mechanical properties.Keywords: polymer composite; mechanical properties; shape memory properties; thermodynamics IntroduceAs a new smart material having broad application space, according to differences of recovery stimulation, shape memory polymers (SMPs) can be divided into the following groups: thermo-responsive SMPs, chemo-responsive SMPs and photo-responsive SMPs [1-3]. Compared with shape memory alloys (SMAs), SMPs have done well in many aspects such as light weight, large recovery ability [4], excellent molding ability [5] and low cost [6]. In recent years, SMPs have been under development in some new fields such as functional clothing [7], information carriers [8,9], two-way actuators [10][11][12] and active assembly/disassembly [13]. Although there is a wide variety of SMPs, thermo-responsive SMPs are still the most basic and the most common SMP materials [14][15][16].The thermomechanical deformation process of SMPs is schematically shown in Figure 1. The thermomechanical deformation process of SMPs consists of the following steps: (1) heat and deform SMP above the transition temperature T trans ; (2) cool SMP until below T trans and remove the applying force; (3) heat the pre-deformed SMP above T trans and then it will recover to its original shape; (4) cool SMP below T trans with its original shape kept. A 3D stress-strain-temperature diagram illustrating the thermomechanical behavior of SMPs is shown in Figure 2 and the thermomechanical behavior of SMPs can be illustrated in four steps [17][18][19]. The first step (state A→B) is a high-temperature deformation state. At this step, the elastic modulus of the SMP is low, the fracture elongation is large, and some of the SMP material shows obvious viscoelastic properties. The second step (state B→C) is a