Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94143.
Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94143;
Proc Natl Acad Sci U S A. 2021 Feb 23;118(8). doi: 10.1073/pnas.2018809118.
N terminomics is a powerful strategy for profiling proteolytic neo-N termini, but its application to cell surface proteolysis has been limited by the low relative abundance of plasma membrane proteins. Here we apply plasma membrane-targeted subtiligase variants (subtiligase-TM) to efficiently and specifically capture cell surface N termini in live cells. Using this approach, we sequenced 807 cell surface N termini and quantified changes in their abundance in response to stimuli that induce proteolytic remodeling of the cell surface proteome. To facilitate exploration of our datasets, we developed a web-accessible Atlas of Subtiligase-Captured Extracellular N Termini (ASCENT; http://wellslab.org/ascent). This technology will facilitate greater understanding of extracellular protease biology and reveal neo-N termini biomarkers and targets in disease.
N 端组学是一种用于分析蛋白水解新生 N 端肽的强大策略,但由于质膜蛋白的相对丰度较低,其在细胞表面蛋白水解中的应用受到限制。在这里,我们应用质膜靶向的枯草溶菌素变体(枯草溶菌素-TM)在活细胞中有效地、特异性地捕获细胞表面 N 端。使用这种方法,我们对 807 个细胞表面 N 端进行了测序,并定量了它们在响应诱导细胞表面蛋白质组发生蛋白水解重塑的刺激时的丰度变化。为了便于探索我们的数据集,我们开发了一个可在线访问的枯草溶菌素捕获细胞外 N 端图谱 (ASCENT; http://wellslab.org/ascent)。这项技术将有助于更好地理解细胞外蛋白酶生物学,并揭示疾病中的新 N 端生物标志物和靶标。