Alvarez-Pardo Rodrigo, Tom Dieck Susanne, Desch Kristina, Nassim Assir Belquis, Olmedo Salinas Cristina, Sivakumar Riya S, Langer Julian D, Schuman Erin M, Alvarez-Castelao Beatriz
Biochemistry and Molecular Biology Department, Veterinary School, Complutense University of Madrid, Madrid, Spain.
Max Planck Institute for Brain Research, Frankfurt am Main, Germany.
Lab Anim (NY). 2025 Aug 13. doi: 10.1038/s41684-025-01589-2.
The functional diversity of cells is driven by the different proteins they express. While improvements in protein labeling techniques have enabled the measurement of proteomes with increased sensitivity, measuring cell type-specific proteomes in vivo remains challenging. One of the most useful pipelines is bio-orthogonal noncanonical amino acid tagging (BONCAT) with the MetRS* system, consisting of a transgenic mouse line expressing a mutant methionyl-tRNA synthetase (MetRS*) controlled by Cre recombinase expression. This system allows cell type-specific labeling of proteins with a noncanonical amino acid (azidonorleucine, ANL), which can be subsequently conjugated to affinity or fluorescent tags using click chemistry. Click-modified proteins can then be visualized, purified and identified. The reduction in sample complexity enables the detection of small changes in protein composition. Here, we describe a multicopy MetRS* mouse line (3xMetRS* mouse line) that exhibits markedly enhanced ANL protein labeling, boosting the sensitivity and temporal resolution of the system and eliminating the need for working under methionine depletion conditions. Cell type-specific in vivo labeling is possible even in heterozygous animals, thus offering an enormous advantage for crossing the line into mutation and disease-specific backgrounds. Using the 3xMetRS* line, we identified the in vivo proteome of a sparse cell population-the dopaminergic neurons of the olfactory bulb-and furthermore determined newly synthesized proteins after short labeling durations following a single intraperitoneal ANL injection.
细胞的功能多样性由其表达的不同蛋白质驱动。虽然蛋白质标记技术的改进使蛋白质组的测量灵敏度有所提高,但在体内测量细胞类型特异性蛋白质组仍然具有挑战性。最有用的方法之一是使用MetRS系统进行生物正交非标准氨基酸标记(BONCAT),该系统由一个转基因小鼠品系组成,该品系表达受Cre重组酶表达控制的突变甲硫氨酰-tRNA合成酶(MetRS)。该系统允许用非标准氨基酸(叠氮亮氨酸,ANL)对蛋白质进行细胞类型特异性标记,随后可使用点击化学将其与亲和或荧光标签缀合。然后可以对点击修饰的蛋白质进行可视化、纯化和鉴定。样品复杂性的降低使得能够检测蛋白质组成的微小变化。在这里,我们描述了一种多拷贝MetRS小鼠品系(3xMetRS小鼠品系),它表现出明显增强的ANL蛋白质标记,提高了系统的灵敏度和时间分辨率,并且无需在甲硫氨酸缺失条件下工作。即使在杂合动物中也可以进行细胞类型特异性的体内标记,因此对于将该品系与突变和疾病特异性背景进行杂交具有巨大优势。使用3xMetRS*品系,我们鉴定了一个稀疏细胞群体——嗅球多巴胺能神经元的体内蛋白质组,此外还确定了在单次腹腔注射ANL后短时间标记后的新合成蛋白质。