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231226s2022 xx |||||o 00| ||eng c |
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|a 10.1021/acs.langmuir.2c00841
|2 doi
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|a pubmed24n1141.xml
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|a (NLM)35737817
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|a eng
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|a Abadian, Hagop
|e verfasserin
|4 aut
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|a Leucine on Silica
|b A Combined Experimental and Modeling Study of a System Relevant for Origins of Life, and the Role of Water Coadsorption
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|c 2022
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 07.07.2022
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|a Date Revised 24.08.2022
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Leucine on silica constitutes an interesting system from the point of view of origins of life studies since leucine coadsorbed on SiO2 together with glutamic acid can give rise to rather long linear polypeptides upon activation. It is also an ideal system to test methods of molecular characterization of biomolecules deposited on mineral surfaces since it combines a small-scale model of peptides and proteins, which are among the most important components of biodevices, with one of the most widely used inorganic materials. We have deposited l-leucine on a high surface fumed silica in the submonolayer range and characterized it by a multipronged approach including macroscopic information (thermogravimetry, X-ray diffraction), in situ spectroscopic methods (IR, multinuclear solid-state NMR including single-pulse and CP-MAS, 2-D HETCOR), and molecular modeling by density functional theory (DFT), including calculation of NMR parameters. Specific information can be obtained on the adsorption and interaction mechanism. Leucine is rather strongly adsorbed without any covalent bonds, through the formation of a specific lattice of H-bonds that often involve coadsorbed water molecules. Its state is indeed strongly dependent on the drying procedure: insufficient drying results in liquid-like surroundings for the leucine functional groups, while vacuum drying only retains a limited number of waters (of the order of 5 per leucine molecule). The most stable models have zwitterionic leucine interacting directly with surface silanols through their ammonium group, while the carboxylate interacts through bridging waters. Experimental NMR chemical shifts are satisfactorily predicted for these models, and leucine can be viewed as a probe for specific groups of surface sites known as silanol nests
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Peptides
|2 NLM
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|a Water
|2 NLM
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|a 059QF0KO0R
|2 NLM
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|a Silicon Dioxide
|2 NLM
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|a 7631-86-9
|2 NLM
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|a Leucine
|2 NLM
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|a GMW67QNF9C
|2 NLM
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|a Cornette, Pauline
|e verfasserin
|4 aut
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|a Costa, Dominique
|e verfasserin
|4 aut
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|a Mezzetti, Alberto
|e verfasserin
|4 aut
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|a Gervais, Christel
|e verfasserin
|4 aut
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|a Lambert, Jean-François
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 38(2022), 26 vom: 05. Juli, Seite 8038-8053
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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|g volume:38
|g year:2022
|g number:26
|g day:05
|g month:07
|g pages:8038-8053
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|u http://dx.doi.org/10.1021/acs.langmuir.2c00841
|3 Volltext
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