Department of Molecular and Cellular Biology, College of Biological Sciences, University of Guelph, 50 Stone Road E, Guelph, ON N1G 2W1, Canada.
Department of Molecular and Cellular Biology, College of Biological Sciences, University of Guelph, 50 Stone Road E, Guelph, ON N1G 2W1, Canada.
STAR Protoc. 2024 Jun 21;5(2):103068. doi: 10.1016/j.xpro.2024.103068. Epub 2024 May 17.
S-acylation, commonly palmitoylation, is the addition of fatty acids to cysteines to regulate protein localization and function. S-acylation detection has been hampered by limited sensitivity and selectivity in low-protein, costly samples like cultured neurons. Here, we present a protocol for sensitive and selective bioorthogonal labeling and click-chemistry-based detection of S-acylated proteins in primary hippocampal neurons. We describe steps for metabolically labeling neurons with alkynyl fatty acid, click chemistry, NeutrAvidin-based capture, and elution with hydroxylamine.
S-酰化,通常是棕榈酰化,是将脂肪酸添加到半胱氨酸上以调节蛋白质的定位和功能。由于在培养神经元等低蛋白、昂贵的样本中,检测的灵敏度和选择性有限,S-酰化的检测一直受到阻碍。在这里,我们提出了一种在原代海马神经元中灵敏和选择性的生物正交标记和点击化学检测 S-酰化蛋白的方案。我们描述了用炔基脂肪酸、点击化学、链霉亲和素捕获和羟胺洗脱对神经元进行代谢标记的步骤。