日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Lipid Pocket Binders Impose Allosteric Changes of Protein Dynamics Around the Active Site of the Protein Kinase p38α

脂质口袋结合物引起蛋白激酶p38α活性位点周围蛋白质动力学的变构变化

Medina Gómez, Sara; Homberg, Laurin T; Bührmann, Mike; Rauh, Daniel; Linser, Rasmus

Luminescent Chiral Molecular Glasses by Melt-Quenching Enantiopure BINAP

通过熔融淬火法制备对映体纯BINAP发光手性分子玻璃

Krittametaporn, Nuttaporn; Ralle, Philipp; Dierks, Dorothea; Nelle, Christian; Vasa, Suresh K; Kolodzeiski, Pascal; Linser, Rasmus; Steffen, Andreas; Henke, Sebastian

Mammalian Proteome Profiling Reveals Readers and Antireaders of Strand-Symmetric and -Asymmetric 5-Hydroxymethylcytosine-Modifications in DNA

哺乳动物蛋白质组分析揭示了DNA中链对称和链不对称5-羟甲基胞嘧啶修饰的读取器和反读取器

Engelhard, Lena; Cakil, Zeyneb Vildan; Zambrano-Mila, Marlon S; Eppmann, Simone; Gonzalez, Tye; Linser, Rasmus; Janning, Petra; Becker, Sidney; Summerer, Daniel

Activation of a Secondary-Messenger Receptor via Allosteric Modulation of a Dynamic Conformational Ensemble

通过动态构象集合的变构调节激活第二信使受体

Söldner, Benedikt; Singh, Himanshu; Akoury, Elias; Witte, Gregor; Linser, Rasmus

Drop Dilution Enables the Use of PEG-Derived Detergents for Membrane Protein Purification

液滴稀释法使得使用PEG衍生的去垢剂进行膜蛋白纯化成为可能

Alker, Katharina; Singh, Shweta; Vinodakrishnan, Arun K; Lindemann, Florian; Linser, Rasmus; Singh, Ram; Singh, Abhishek K; Urner, Leonhard H

Assignment of the N-terminal domain of mouse cGAS

小鼠 cGAS N 端结构域的分配

Aucharova, Hanna; Linser, Rasmus

Transient Structural Properties of the Rho GDP-Dissociation Inhibitor

Rho GDP解离抑制剂的瞬态结构特性

Medina Gomez, Sara; Visco, Ilaria; Merino, Felipe; Bieling, Peter; Linser, Rasmus

Highly porous metal-organic framework liquids and glasses via a solvent-assisted linker exchange strategy of ZIF-8

通过溶剂辅助配体交换策略制备高孔隙率金属有机框架液体和玻璃态 ZIF-8

Xue, Wen-Long; Kolodzeiski, Pascal; Aucharova, Hanna; Vasa, Suresh; Koutsianos, Athanasios; Pallach, Roman; Song, Jianbo; Frentzel-Beyme, Louis; Linser, Rasmus; Henke, Sebastian

Sedimentation of large, soluble proteins up to 140 kDa for 1H-detected MAS NMR and 13C DNP NMR - practical aspects

1H 检测 MAS NMR 和 13C DNP NMR 中高达 140 kDa 的大型可溶性蛋白质的沉淀 - 实用方面

Dallas Bell, Florian Lindemann, Lisa Gerland, Hanna Aucharova, Alexander Klein, Daniel Friedrich, Matthias Hiller, Kristof Grohe, Tobias Meier, Barth van Rossum, Anne Diehl, Jon Hughes, Leonard J Mueller, Rasmus Linser, Anne-Frances Miller, Hartmut Oschkinat

Sedimentation of large, soluble proteins up to 140 kDa for (1)H-detected MAS NMR and (13)C DNP NMR - practical aspects

用于 (1)H 检测 MAS NMR 和 (13)C DNP NMR 的大分子可溶性蛋白质(分子量高达 140 kDa)的沉降——实用性方面

Bell, Dallas; Lindemann, Florian; Gerland, Lisa; Aucharova, Hanna; Klein, Alexander; Friedrich, Daniel; Hiller, Matthias; Grohe, Kristof; van Rossum, Barth; Diehl, Anne; Hughes, Jon; Mueller, Leonard J; Linser, Rasmus; Miller, Anne-Frances; Oschkinat, Hartmut