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The glycoprotein gp41 from the Human Immunodeficiency Virus type 1 (HIV-1) has an amino acid sequence enriched in tryptophan residues, the so-called gp41W peptide (i.e., KWASLWNWFNITNWLWYIK) and plays a crucial role in HIV-1 host cell infection. Using the coupling of Second Harmonic Generation targeting the tryptophan residues with lateral surface tension measurements, we investigate the interaction of gp41W with a neat air∕water and a lipid∕water interfaces. At the air∕water interface, gp41W presents a well-defined orientation and this orientation is strongly modified at the lipid∕water interface, depending on the surface pressure. These results show that this strategy is well suited to monitor tryptophan containing α-helices orientation at lipid∕water interfaces.

On the basis of our previous work on vinyl-triphenylamine derived DNA fluorophores we explored the structure space around this core by coupling it to diverse cationic, anionic and zwitterionic groups in the aim of targeting different classes of biomolecules. In parallel core modifications were performed to optimize the photophysical properties (quantum yield, two-photon absorption). The resulting water soluble π-conjugated molecules are called TP dyes and display an exceptional combination of optical properties: high two-photon absorption cross-section, high photostability, no self-quenching, and switchable fluorescence emission when bound to a biopolymer matrix. The linear and nonlinear optical properties of the TP dyes were studied in vitro in presence of DNA and in presence of a model protein (human serum albumin) using complementary absorption and fluorescence spectroscopy characterization tools. Structure modifications enabled to switch from DNA probes (cationic TP-pyridinium series) to protein probes (anionic TP-rhodanine series) without affecting the optical properties. Finally most TP compounds appear cell-permeant and show an intracellular localization consistent with their in vitro target specificity.

We have measured the first hyperpolarizabilities of thioalkane capped silver and gold metallic nanoparticles. The values found are β(AgC 12-10 nm) = (2.10 ± 0.23) × 10(-26) esu for 10 nm diameter silver nanoparticles and β(AuC 18-18 nm) = (3.37 ± 0.08) × 10(-26) esu for 18 nm diameter gold nanoparticles at the fundamental wavelength of 784 nm. By comparison to the corresponding values reported for citrate capped silver and gold metallic nanoparticles, after size corrections, decreases by factors of 4.3 and 6.5 respectively are observed. These decreases are tentatively attributed to the bonds formed between the gold and silver surface atoms and the sulfur atoms of the capping layer., (© 2012 IOP Publishing Ltd)