Armbruster Krista M, Meredith Timothy C
Department of Biochemistry and Molecular Biology, Pennsylvania State University.
Department of Biochemistry and Molecular Biology, Pennsylvania State University;
J Vis Exp. 2018 May 21(135):56842. doi: 10.3791/56842.
Lipoproteins are important constituents of the bacterial cell envelope and potent activators of the mammalian innate immune response. Despite their significance to both cell physiology and immunology, much remains to be discovered about novel lipoprotein forms, how they are synthesized, and the effect of the various forms on host immunity. To enable thorough studies on lipoproteins, this protocol describes a method for bacterial lipoprotein enrichment and preparation of N-terminal tryptic lipopeptides for structural determination by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS). Expanding on an established Triton X-114 phase partitioning method for lipoprotein extraction and enrichment from the bacterial cell membrane, the protocol includes additional steps to remove non-lipoprotein contaminants, increasing lipoprotein yield and purity. Since lipoproteins are commonly used in Toll-like receptor (TLR) assays, it is critical to first characterize the N-terminal structure by MALDI-TOF MS. Herein, a method is presented to isolate concentrated hydrophobic peptides enriched in N-terminal lipopeptides suitable for direct analysis by MALDI-TOF MS/MS. Lipoproteins that have been separated by Sodium Dodecyl Sulfate Poly-Acrylamide Gel Electrophoresis (SDS-PAGE) are transferred to a nitrocellulose membrane, digested in situ with trypsin, sequentially washed to remove polar tryptic peptides, and finally eluted with chloroform-methanol. When coupled with MS of the more polar trypsinized peptides from wash solutions, this method provides the ability to both identify the lipoprotein and characterize its N-terminus in a single experiment. Intentional sodium adduct formation can also be employed as a tool to promote more structurally informative fragmentation spectra. Ultimately, enrichment of lipoproteins and determination of their N-terminal structures will permit more extensive studies on this ubiquitous class of bacterial proteins.
脂蛋白是细菌细胞膜的重要组成部分,也是哺乳动物固有免疫反应的强效激活剂。尽管它们对细胞生理学和免疫学都很重要,但关于新型脂蛋白形式、它们如何合成以及各种形式对宿主免疫的影响,仍有许多有待发现之处。为了能够对脂蛋白进行全面研究,本方案描述了一种细菌脂蛋白富集方法以及制备N端胰蛋白酶解脂肽的方法,用于通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)进行结构测定。该方案在已建立的用于从细菌细胞膜中提取和富集脂蛋白的Triton X-114相分配方法的基础上进行了扩展,包括去除非脂蛋白污染物的额外步骤,提高了脂蛋白的产量和纯度。由于脂蛋白常用于Toll样受体(TLR)检测,因此首先通过MALDI-TOF MS表征N端结构至关重要。本文介绍了一种分离浓缩的富含N端脂肽的疏水肽的方法,适用于通过MALDI-TOF MS/MS直接分析。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分离的脂蛋白转移到硝酸纤维素膜上,用胰蛋白酶原位消化,依次洗涤以去除极性胰蛋白酶肽,最后用氯仿-甲醇洗脱。当与来自洗涤溶液的极性更强的胰蛋白酶化肽的质谱联用,该方法能够在单个实验中识别脂蛋白并表征其N端。有意形成钠加合物也可以用作促进更具结构信息的碎裂谱的工具。最终,脂蛋白的富集及其N端结构的测定将允许对这类普遍存在的细菌蛋白进行更广泛的研究。