Background-There is an urgent need to determine whether oversulfated chondroitin sulfate (OSCS), a compound contaminating heparin supplies worldwide, is the cause of the severe anaphylactoid reactions that have occurred after intravenous heparin administration in the United States and Germany.

The precise delivery of male to female gametes during reproduction in eukaryotes requires complex signal exchanges and a flawless communication between male and female tissues. In angiosperms, molecular mechanisms have recently been revealed that are crucial for the dialog between male (pollen tube) and female gametophytes required for successful sperm delivery. When pollen tubes reach the female gametophyte, they arrest growth, burst and discharge their sperm cells. These processes are under the control of the female gametophyte via the receptor-like serine-threonine kinase (RLK) FERONIA(FER). However, the male signaling components that control the sperm delivery remain elusive. Here, we show that ANXUR1 and ANXUR2(ANX1, ANX2), which encode the closest homologs of the FER-RLK in Arabidopsis, are preferentially expressed in pollen. Moreover,ANX1-YFP and ANX2-YFP fusion proteins display polar localization to the plasma membrane at the tip of the pollen tube. Finally, genetic analyses demonstrate that ANX1 and ANX2 function redundantly to control the timing of pollen tube discharge as anx1 anx2 double-mutant pollen tubes cease their growth and burst in vitro and fail to reach the female gametophytes in vivo. We propose that ANX-RLKs constitutively inhibit pollen tube rupture and sperm discharge at the tip of growing pollen tubes to sustain their growth within maternal tissues until they reach the female gametophytes. Upon arrival, the female FER-dependent signaling cascade is activated to mediate pollen tube reception and fertilization, while male ANX-dependent signaling is deactivated, enabling the pollen tube to rupture and deliver its sperm cells to effect fertilization.

Heparan sulfate proteoglycans (HSPGs) play a key role in shaping the tumor microenvironment by presenting growth factors, cytokines, and other soluble factors that are critical for host cell recruitment and activation, as well as promoting tumor progression, metastasis, and survival. M402 is a rationally engineered, non-cytotoxic heparan sulfate (HS) mimetic, designed to inhibit multiple factors implicated in tumor-host cell interactions, including VEGF, FGF2, SDF-1α, P-selectin, and heparanase. A single s.c. dose of M402 effectively inhibited seeding of B16F10 murine melanoma cells to the lung in an experimental metastasis model. Fluorescent-labeled M402 demonstrated selective accumulation in the primary tumor. Immunohistological analyses of the primary tumor revealed a decrease in microvessel density in M402 treated animals, suggesting anti-angiogenesis to be one of the mechanisms involved in-vivo. M402 treatment also normalized circulating levels of myeloid derived suppressor cells in tumor bearing mice. Chronic administration of M402, alone or in combination with cisplatin or docetaxel, inhibited spontaneous metastasis and prolonged survival in an orthotopic 4T1 murine mammary carcinoma model. These data demonstrate that modulating HSPG biology represents a novel approach to target multiple factors involved in tumor progression and metastasis.

A new biomimetic route for the synthesis of a conducting molecular complex of polyaniline (Pani) and a natural polyelectrolyte, lignosulfonate (LGS) is presented. A poly(ethylene glycol) modified hematin (PEG-hematin) was used to catalyze the polymerization of aniline in the presence of LGS to form a Pani/LGS complex. UV-vis, FTIR, conductivity and TGA studies for the LGS-polyaniline complex indicate the presence of a thermally stable and electrically conductive form of polyaniline. Also the presence of LGS in this complex, an inexpensive byproduct from pulp processing, provides a unique combination of properties such as electronic conductivity, processability and biodegradability. The use of this conductive complex for corrosion protection is also proposed.

We present a surface x-ray analysis of the atomic structure of the (0001) surface of the topological insulator Bi 2 Se 3 , which was grown as a single crystal and as an ultrathin film on Si(111) using molecular beam epitaxy (MBE). In general we find that the top Se-Bi layer spacing is expanded between 2% and 17% relative to the bulk, while deeper layers and the first van der Waals gap are unrelaxed. The top layer expansion is directly related to the amount of surface contamination by carbon and oxygen. The near-surface structures of the single crystal and the MBE-grown thin film differ in the degree of (static) disorder: for the former an overall Debye parameter (B) per quintuple layer (QL) of 5Å 2 is found to decrease slowly with depth. MBE-grown Bi 2 Se 3 films exhibit the opposite scenario, characterized by an increase in B from about 10Å 2 for the topmost QL to values of B = 20-40Å 2 for the fourth QL. This is attributed to the lattice misfit to the Si(111) surface. Ab initio calculations reveal carbon to act as an n-dopant, while the first interlayer spacing expansion induces a shift of the Dirac point towards the Bi 2 Se 3 bulk conduction band minimum.

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The variation in molecular and electronic structure of doped (as synthesized) conducting, dedoped base, and redoped conducting forms of polyaniline (PANI) prepared by oxidative enzymatic polymerization of aniline with and without the presence of polyelectrolyte template was analyzed by solid-state 13 C and 15 N CP/MAS NMR spectroscopy. Polyanilines were enzymatically synthesized using a natural biocatalyst such as horseradish peroxidase (HRP) at pH 4.3 and a synthetic biomimetic catalyst, specifically poly(ethylene glycol)-coupled hematin (PEG-hematin), at pH 1.0. The HRP-catalyzed enzymatic polymerization of PANI was carried out in the presence of macromolecular polyelectrolyte templates such as poly(vinylphosphonic acid) (PVP), poly(4-styerenesulfonate) (SPS), and dodecylbenzenesulfonic acid (DBSA). 13 C and 15 N CP/MAS NMR spectral features indicate that the PANI obtained by PEG-hematincatalyzed enzymatic polymerization resembles most with chemically synthesized analogues in its doped (as synthesized) conducting form than other forms of PANI. A systematic experiment involving a redoping process at different pH levels shows the structural changes during the transformation from dedoped base form to redoped conducting form. Solid-state NMR data also indicate a decrease of polaronic contribution at the higher doping level. End-group analysis from 15 N CP/MAS NMR data provides information on the molecular weight of the enzymatically polymerized PANI sample.

Angular resolved photoemission spectroscopy in combination with ab initio calculations show that trace amounts of carbon doping of the Bi_{2}Se_{3} surface allows the controlled shift of the Dirac point within the bulk band gap. In contrast to expectation, no Rashba-split two-dimensional electron gas states appear. This unique electronic modification is related to surface structural modification characterized by an expansion of the top Se-Bi spacing of ≈11% as evidenced by surface x-ray diffraction. Our results provide new ways to tune the surface band structure of topological insulators.