Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Leendert van Dalsen"'
Autor:
Abhishek Dewanji, Leendert van Dalsen, James A. Rossi-Ashton, Eloise Gasson, Giacomo E. M. Crisenza, David J. Procter
Publikováno v:
Nature Chemistry. 15:43-52
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49f8973c1a042127e3da26233f5e430f
https://doi.org/10.1038/s41557-022-01092-y
https://doi.org/10.1038/s41557-022-01092-y
Publikováno v:
Angewandte Chemie International Edition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a091d2f14d2442f156e232082405411
https://doi.org/10.1002/anie.202303104
https://doi.org/10.1002/anie.202303104
Publikováno v:
Crystal Growth & Design. 21:490-500
Monoolein, also referred to as 9.9 MAG, is the most commonly used monoacylglycerol for crystallizing membrane proteins by the in meso method. However, 9.9 MAG does not work for all proteins. Theref...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb413093ab8088040852c8d9e03800d8
https://doi.org/10.1021/acs.cgd.0c01301
https://doi.org/10.1021/acs.cgd.0c01301
Autor:
Luke Smithers, Gerard Reid, Leendert van Dalsen, Coilin Boland, Dietmar Weichert, Martin Caffrey
Publikováno v:
Crystal Growth & Design. 20:5444-5454
Monoacylglycerols (MAGs) are the lipids most commonly used for crystallizing membrane proteins by the in meso method. The acyl chain and glycerol components of MAGs are ester-linked at the sn-1 hyd...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9ce2b0cf203d86cdd8216c2ef771b03
https://doi.org/10.1021/acs.cgd.0c00660
https://doi.org/10.1021/acs.cgd.0c00660
Publikováno v:
Journal of Applied Crystallography
The lipid cubic phase is compatible with the synthetic digitonin analogue, GDN, over a considerable range of concentrations, indeed well beyond those likely to be encountered in typical membrane crystallization studies. Thus, based on its compatibili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89c3d596207d23e3545ae56d53515486
http://europepmc.org/articles/PMC7133060
http://europepmc.org/articles/PMC7133060
Autor:
Abhishek Dewanji, Leendert van Dalsen, James Rossi-Ashton, Eloise Gasson, Giacomo Crisenza, David Procter
The photoactivation of electron donor-acceptor (EDA) complexes has emerged as a sustainable, selective and versa-tile strategy for the generation of radical species. However, when it comes to aryl radical formation, this strategy remains hamstrung by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b67a590aa5a1ee2b59308e669c23d217
https://doi.org/10.26434/chemrxiv-2021-xbn7k
https://doi.org/10.26434/chemrxiv-2021-xbn7k
Autor:
Abhishek, Dewanji, Leendert, van Dalsen, James A, Rossi-Ashton, Eloise, Gasson, Giacomo E M, Crisenza, David J, Procter
Publikováno v:
Nature chemistry.
The photoactivation of electron donor-acceptor complexes has emerged as a sustainable, selective and versatile strategy for the generation of radical species. However, when it comes to aryl radical formation, this strategy remains hamstrung by the el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::820dca80334b4c4da7988e0f78082c5c
https://pubmed.ncbi.nlm.nih.gov/36471045
https://pubmed.ncbi.nlm.nih.gov/36471045