Nanoscale defolding influence of polypeptides in the charge-transfer process through an organic-inorganic nanohybrid system.

A biologically important polypeptide [with an alternate sequence of alanine (ALA) and 2-aminobutyric acid (AiB)] is used as a linker molecule to investigate the charge-transfer phenomenon between CdSe nanoparticle (NP) (diameter ∼6-7 nm) assemblies and gold (Au) substrates. The (ALA-AiB)n polypeptides, with varying chain lengths n = 5, 8, 11, were attached to the surface to form self-assembled monolayers (SAMs) through a thiol group located either at the N-terminal or C-terminal of the sequence. Temperature dependent photoluminescence (PL) spectra showed anomalous behavior in the quenching regime of CdSe NPs in the 237 K to 290 K region.

Chirality Dependent Charge Transfer Rate in Oligopeptides.

It is shown that "spontaneous magnetization" occurs when chiral oligopeptides are attached to ferrocene and are self-assembled on a gold substrate. As a result, the electron transfer, measured by electrochemistry, shows asymmetry in the reduction and oxidation rate constants; this asymmetry is reversed between the two enantiomers. The results can be explained by the chiral induced spin selectivity of the electron transfer.

The electron's spin and molecular chirality - how are they related and how do they affect life processes?

The recently discovered chiral induced spin selectivity (CISS) effect gives rise to a spin selective electron transmission through biomolecules. Here we review the mechanism behind the CISS effect and its implication for processes in Biology. Specifically, three processes are discussed: long-range electron transfer, spin effects on the oxidation of water, and enantioselectivity in bio-recognition events.

Spin-Controlled Photoluminescence in Hybrid Nanoparticles Purple Membrane System.

Spin-dependent photoluminescence (PL) quenching of CdSe nanoparticles (NPs) has been explored in the hybrid system of CdSe NP purple membrane, wild-type bacteriorhodopsin (bR) thin film on a ferromagnetic (Ni-alloy) substrate. A significant change in the PL intensity from the CdSe NPs has been observed when spin-specific charge transfer occurs between the retinal and the magnetic substrate. This feature completely disappears in a bR apo membrane (wild-type bacteriorhodopsin in which the retinal protein covalent bond was cleaved), a bacteriorhodopsin mutant (D96N), and a bacteriorhodopsin bearing a locked retinal chromophore (isomerization of the crucial C13═C14 retinal double bond was prevented by inserting a ring spanning this bond).

A device for measuring spin selectivity in electron transfer.

A new type of device is presented that allows direct measurement of spin selectivity in charge transfer processes occurring in adsorbed molecules. The new device provides direct information about the nature of the charge being transferred (electrons or holes) and on spin selectivity, if it exists. Here the device is applied for establishing the spin-dependent electron transfer through double-stranded DNA and its variation with the length of the oligomer.