| 1. |
- Liu, Tao, et al.
(författare)
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Understanding LiOH Formation in a Li-O2 Battery with LiI and H2O Additives
- 2019
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Ingår i: ACS Catalysis. - : American Chemical Society (ACS). - 2155-5435. ; 9:1, s. 66-77
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Tidskriftsartikel (refereegranskat)abstract
- LiI-promoted LiOH formation in Li-O2 batteries with wet ether electrolytes has been investigated by Raman, nuclear magnetic resonance spectroscopy, operando pressure tests, and molecular dynamics simulations. We find that LiOH formation is a synergistic effect involving both H2O and LiI additives, whereas with either alone Li2O2 forms. LiOH is generated via a nominal four-electron oxygen reduction reaction, the hydrogen coming from H2O and the oxygen from both O2 and H2O, and with fewer side reactions than typically associated with Li2O2 formation; the presence of fewer parasitic reactions is attributed to the proton donor role of water, which can coordinate to O2- and the higher chemical stability of LiOH. Iodide plays a catalytic role in decomposing H2O2/HO2- and thereby promoting LiOH formation, its efficacy being highly dependent on the water concentration. This iodide catalysis becomes retarded at high water contents due to the formation of large water-solvated clusters, and Li2O2 forms again.
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| 2. |
- Nilsson, IngMarie, et al.
(författare)
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Photocross-linking of nascent chains to the STT3 subunit of the oligosaccharyltransferase complex
- 2003
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Ingår i: Journal of Cell Biology. - : Rockefeller University Press. - 0021-9525 .- 1540-8140. ; 161:4, s. 715-725
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Tidskriftsartikel (refereegranskat)abstract
- In eukaryotic cells, polypeptides are N glycosylated after passing through the membrane of the ER into the ER lumen. This modification is effected cotranslationally by the multimeric oligosaccharyltransferase (OST) enzyme. Here, we report the first cross-linking of an OST subunit to a nascent chain that is undergoing translocation through, or integration into, the ER membrane. A photoreactive probe was incorporated into a nascent chain using a modified Lys-tRNA and was positioned in a cryptic glycosylation site (-Q-K-T- instead of -N-K-T-) in the nascent chain. When translocation intermediates with nascent chains of increasing length were irradiated, nascent chain photocross-linking to translocon components, Sec61alpha and TRAM, was replaced by efficient photocross-linking solely to a protein identified by immunoprecipitation as the STT3 subunit of the OST No cross-linking was observed in the absence of a cryptic sequence or in the presence of a competitive peptide substrate of the OST. As no significant nascent chain photocross-linking to other OST subunits was detected in these fully assembled translocation and integration intermediates, our results strongly indicate that the nascent chain portion of the OST active site is located in STT3.
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