Dantuluri Swathi, Wu Yifei, Hepowit Nathaniel L, Chen Hui, Chen Sixue, Maupin-Furlow Julie A
Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, USA.
College of Forestry, Northwest A & F University, Yangling, Shaanxi, P. R. China.
Proteomics. 2016 Apr;16(7):1100-10. doi: 10.1002/pmic.201500153.
Small archeal modifier proteins (SAMPs) are related to ubiquitin in tertiary structure and in their isopeptide linkage to substrate proteins. SAMPs also function in sulfur mobilization to form biomolecules such as molybdopterin and thiolated tRNA. While SAMP1 is essential for anaerobic growth and covalently attached to lysine residues of its molybdopterin synthase partner MoaE (K240 and K247), the full diversity of proteins modified by samp1ylation is not known. Here, we expand the knowledge of proteins isopeptide linked to SAMP1. LC-MS/MS analysis of -Gly-Gly signatures derived from SAMP1 S85R conjugates cleaved with trypsin was used to detect sites of sampylation (23 lysine residues) that mapped to 11 target proteins. Many of the identified target proteins were associated with sulfur metabolism and oxidative stress including MoaE, SAMP-activating E1 enzyme (UbaA), methionine sulfoxide reductase homologs (MsrA and MsrB), and the Fe-S assembly protein SufB. Several proteins were found to have multiple sites of samp1ylation, and the isopeptide linkage at SAMP3 lysines (K18, K55, and K62) revealed hetero-SAMP chain topologies. Follow-up affinity purification of selected protein targets (UbaA and MoaE) confirmed the LC-MS/MS results. 3D homology modeling suggested sampy1ylation is autoregulatory in inhibiting the activity of its protein partners (UbaA and MoaE), while occurring on the surface of some protein targets, such as SufB and MsrA/B. Overall, we provide evidence that SAMP1 is a ubiquitin-like protein modifier that is relatively specific in tagging its protein partners as well as proteins associated with oxidative stress response.
小型古菌修饰蛋白(SAMPs)在三级结构以及与底物蛋白的异肽键连接方面与泛素相关。SAMPs在硫的动员中也发挥作用,以形成生物分子,如钼辅因子和硫醇化tRNA。虽然SAMP1对厌氧生长至关重要,并共价连接到其钼辅因子合酶伴侣MoaE的赖氨酸残基(K240和K247)上,但被SAMP1化修饰的蛋白质的全部多样性尚不清楚。在这里,我们扩展了与SAMP1异肽键连接的蛋白质的知识。通过对用胰蛋白酶切割的SAMP1 S85R缀合物衍生的-Gly-Gly信号进行LC-MS/MS分析,以检测SAMP1化修饰位点(23个赖氨酸残基),这些位点映射到11个靶蛋白上。许多鉴定出的靶蛋白与硫代谢和氧化应激相关,包括MoaE、SAMP激活E1酶(UbaA)、甲硫氨酸亚砜还原酶同源物(MsrA和MsrB)以及铁硫组装蛋白SufB。发现几种蛋白质有多个SAMP1化修饰位点,并且SAMP3赖氨酸(K18、K55和K62)处的异肽键连接揭示了杂合SAMP链拓扑结构。对选定的蛋白质靶标(UbaA和MoaE)进行的后续亲和纯化证实了LC-MS/MS结果。三维同源建模表明,SAMP1化修饰在抑制其蛋白质伴侣(UbaA和MoaE)的活性方面具有自我调节作用,同时发生在一些蛋白质靶标的表面,如SufB和MsrA/B。总体而言,我们提供的证据表明,SAMP1是一种类泛素蛋白修饰剂,在标记其蛋白质伴侣以及与氧化应激反应相关的蛋白质方面相对具有特异性。