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Livia Salvati Manni

Researcher at University of Zurich

Publications -  15
Citations -  231

Livia Salvati Manni is an academic researcher from University of Zurich. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 7, co-authored 12 publications receiving 150 citations. Previous affiliations of Livia Salvati Manni include University of Sydney & Sapienza University of Rome.

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Soft biomimetic nanoconfinement promotes amorphous water over ice.

TL;DR: A specifically designed family of synthetic lipids with designed cyclopropyl modifications in the hydrophobic chains that exhibit unique liquid-crystalline behaviour at low temperature, enabling maintenance of amorphous water down to about 10 K due to nanoconfinement is introduced.
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Lipidic Mesophases as Novel Nanoreactor Scaffolds for Organocatalysts: Heterogeneously Catalyzed Asymmetric Aldol Reactions in Confined Water

TL;DR: These mesophases can be recycled and enable efficient catalytic activity as well as modulation of the diastereo- and enantioselectivity for the aldol reaction of several benzaldehyde derivatives and cyclohexanone in water.
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Phase Behavior of a Designed Cyclopropyl Analogue of Monoolein: Implications for Low‐Temperature Membrane Protein Crystallization

TL;DR: Small-angle X-ray scattering analyses revealed a phase diagram for MDS lacking the high-temperature, highly curved reverse hexagonal phase typical for MO, and extending the cubic phase boundary to lower temperature, thereby establishing the relationship between lipid molecular structure and mesophase behavior.
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A macroscopic H+ and Cl− ions pump via reconstitution of EcClC membrane proteins in lipidic cubic mesophases

TL;DR: A general strategy to demonstrate correct functional reconstitution of active and selective membrane protein transporters in lipidic mesophases, exemplified by the bacterial ClC exchanger from Escherichia coli as a model ion transporter is designed.
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Recognition of concanavalin A by cationic glucosylated liposomes.

TL;DR: Fluorescence experiments demonstrated that the monomeric glucosylated amphiphile is capable of interacting with fluorescently labeled concanavalin A, a D-glucose specific plant lectin, and paved the way to the preparation of other glycosilated amphiphiles differing for the length of polyoxyethylenic spacer, the sugar moieties, and/or thelength of the hydrophobic chain.