45 research outputs found

    Protein-polymer nano-machines. Towards synthetic control of biological processes

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    The exploitation of nature's machinery at length scales below the dimensions of a cell is an exciting challenge for biologists, chemists and physicists, while advances in our understanding of these biological motifs are now providing an opportunity to develop real single molecule devices for technological applications. Single molecule studies are already well advanced and biological molecular motors are being used to guide the design of nano-scale machines. However, controlling the specific functions of these devices in biological systems under changing conditions is difficult. In this review we describe the principles underlying the development of a molecular motor with numerous potential applications in nanotechnology and the use of specific synthetic polymers as prototypic molecular switches for control of the motor function. The molecular motor is a derivative of a TypeI Restriction-Modification (R-M) enzyme and the synthetic polymer is drawn from the class of materials that exhibit a temperature-dependent phase transition. The potential exploitation of single molecules as functional devices has been heralded as the dawn of new era in biotechnology and medicine. It is not surprising, therefore, that the efforts of numerous multidisciplinary teams [1,2]. have been focused in attempts to develop these systems. as machines capable of functioning at the low sub-micron and nanometre length-scales [3]. However, one of the obstacles for the practical application of single molecule devices is the lack of functional control methods in biological media, under changing conditions. In this review we describe the conceptual basis for a molecular motor (a derivative of a TypeI Restriction-Modification enzyme) with numerous potential applications in nanotechnology and the use of specific synthetic polymers as prototypic molecular switches for controlling the motor function [4]

    The syntheses and preparation of materials for the detection of organic volatiles

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    A Tandem Sulfur Transfer/Reduction/Michael Addition Mediated by Benzyltriethylammonium Tetrathiomolybdate

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    Disulfides and sulfur containing organic compounds are important functional groups widely present in nature and have commercial significance.[1] Therefore, the synthesis of disulfides, sulfides, and w-thioketones is not only attractive but also finds numerous applications

    Physico-chemical and pharmacokinetic studies of avidin bioconjugates with thermosensitive polymers.

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    N-isopropilacrylamide-co-acrylamide 6000 Da with a LCST of 37\ub0C, was activated and conjugated to avidin. Gel permeation analysis demonstrated that the polymer conjugation modifies remarkably the protein hydrodynamic volume. The bioconjugate displayed higher LCST compared to the original polymer. The polymer conjugation altered slightly the protein tertiary structure and the binding with both biotin and bionylated antibodies. Pharmacokinetic studies demonstrated that the bioconjugate shows longer permanence in the blood stream as compared to the native protein

    A tandem sulfur transfer/reduction/michael addition mediated by benzyltriethylammonium tetrathiomolybdate

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    Disulfides and sulfur containing organic compounds are important functional groups widely present in nature and have commercial significance.[1] Therefore, the synthesis of disulfides, sulfides, and w-thioketones is not only attractive but also finds numerous applications

    Physicochemical Characterization of Thermoresponsive Poly(N-isopropylacrylamide)−poly(ethylene imine) Graft Copolymers

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    Synthetic polycations have shown promise as gene delivery vehicles but suffer from an unacceptable toxicity and low transfection efficiency. Novel architectures are being explored to increase transfection efficiency, including copolymers with a thermoresponsive character. The physicochemical characterization of a family of copolymers comprising a core of the cationic polymer poly(ethylene imine) (PEI) with differing thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) grafts has been carried out using pulsed-gradient spin–echo NMR (PGSE-NMR) and small-angle neutron scattering (SANS). For the copolymers that have longer chain PNIPAM grafts, there is clear evidence of the collapse of the grafts with increasing temperature and the associated emergence of an attractive interpolymer interaction. These facets depend on the number of PNIPAM grafts attached to the PEI core. While a collapse in the smaller PNIPAM grafts is observed for the third polymer, there is no appearance of the interpolymer attractive interaction. These observations provide further insight into the association behavior of these copolymers, which is fundamental to developing a full understanding of how they interact with nucleic acids. Furthermore, the differing behaviors of the three copolymers over temperatures in which the PNIPAM blocks undergo coil-to-globule transitions is indicative of changes in the presentation of charged-core and hydrophobic chain components, which are key factors affecting nucleic acid binding and, ultimately, cell transfection ability

    Catalytic Aerobic Oxidation of Cycloalkanes with Nanostructured Amorphous Metals and Alloys**

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    The functionalization of unactivated carbon-hydrogen bonds in saturated hydrocarbons has been investigated for both its synthetic and biological interest.[1] Catalytic oxidation of alkanes has been explored using several oxidants,[2] and those reactions with molecular oxygen under mild conditions[3] are especially rewarding goals. The oxidation of cyclohexane turns out to be the least efficient of all major industrial processes.[4
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