Department of Structural and Computational Biology, Max Perutz Labs, Vienna Biocenter Campus 5, 1030, Vienna, Austria.
Present address: Calyxha Biotechnologies GmbH, Karl-Farkas-Gasse 22, 1030, Vienna, Austria.
Angew Chem Int Ed Engl. 2020 Mar 2;59(10):3886-3890. doi: 10.1002/anie.201913585. Epub 2020 Jan 29.
Interactions of transmembrane receptors with their extracellular ligands are essential for cellular communication and signaling and are therefore a major focus in drug discovery programs. The transition from in vitro to live cell interaction studies, however, is typically a bottleneck in many drug discovery projects due to the challenge of obtaining atomic-resolution information under near-physiological conditions. Although NMR spectroscopy is ideally suited to overcome this limitation, several experimental impairments are still present. Herein, we propose the use of methylcellulose hydrogels to study extracellular proteins and their interactions with plasma membrane receptors. This approach reduces cell sedimentation, prevents the internalization of membrane receptors, and increases cell survival, while retaining the free tumbling of extracellular proteins.
跨膜受体与其细胞外配体的相互作用对于细胞通讯和信号转导至关重要,因此是药物发现计划的主要重点。然而,从体外到活细胞相互作用研究的转变通常是许多药物发现项目的瓶颈,因为在接近生理条件下获得原子分辨率信息具有挑战性。尽管 NMR 光谱学非常适合克服这一限制,但仍存在一些实验缺陷。在此,我们提出使用甲基纤维素水凝胶来研究细胞外蛋白及其与质膜受体的相互作用。这种方法减少了细胞沉淀,防止了膜受体的内化,并提高了细胞存活率,同时保持了细胞外蛋白的自由旋转。