Department of Medicinal Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.
Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, USA.
Int J Mol Sci. 2024 May 13;25(10):5324. doi: 10.3390/ijms25105324.
Protein farnesylation is a post-translational modification where a 15-carbon farnesyl isoprenoid is appended to the C-terminal end of a protein by farnesyltransferase (FTase). This process often causes proteins to associate with the membrane and participate in signal transduction pathways. The most common substrates of FTase are proteins that have C-terminal tetrapeptide CaaX box sequences where the cysteine is the site of modification. However, recent work has shown that five amino acid sequences can also be recognized, including the pentapeptides CMIIM and CSLMQ. In this work, peptide libraries were initially used to systematically vary the residues in those two parental sequences using an assay based on Matrix Assisted Laser Desorption Ionization-Mass Spectrometry (MALDI-MS). In addition, 192 pentapeptide sequences from the human proteome were screened using that assay to discover additional extended CaaaX-box motifs. Selected hits from that screening effort were rescreened using an in vivo yeast reporter protein assay. The X-ray crystal structure of CMIIM bound to FTase was also solved, showing that the C-terminal tripeptide of that sequence interacted with the enzyme in a similar manner as the C-terminal tripeptide of CVVM, suggesting that the tripeptide comprises a common structural element for substrate recognition in both tetrapeptide and pentapeptide sequences. Molecular dynamics simulation of CMIIM bound to FTase further shed light on the molecular interactions involved, showing that a putative catalytically competent Zn(II)-thiolate species was able to form. Bioinformatic predictions of tetrapeptide (CaaX-box) reactivity correlated well with the reactivity of pentapeptides obtained from in vivo analysis, reinforcing the importance of the C-terminal tripeptide motif. This analysis provides a structural framework for understanding the reactivity of extended CaaaX-box motifs and a method that may be useful for predicting the reactivity of additional FTase substrates bearing CaaaX-box sequences.
蛋白质法尼基化是一种翻译后修饰过程,其中法尼基转移酶 (FTase) 将一个 15 碳法尼基异戊烯添加到蛋白质的 C 末端。这个过程通常会导致蛋白质与膜结合并参与信号转导途径。FTase 最常见的底物是具有 C 末端四肽 CaaX 盒序列的蛋白质,其中半胱氨酸是修饰的位点。然而,最近的工作表明,也可以识别五个氨基酸序列,包括五肽 CMIIM 和 CSLMQ。在这项工作中,最初使用肽文库通过基于基质辅助激光解吸电离 - 质谱 (MALDI-MS) 的测定来系统地改变这两个亲本序列中的残基。此外,使用该测定法筛选了来自人类蛋白质组的 192 个五肽序列,以发现其他扩展的 CaaaX 盒基序。从该筛选工作中选择的命中物使用体内酵母报告蛋白测定法进行重新筛选。CMIIM 与 FTase 结合的 X 射线晶体结构也得到了解决,表明该序列的 C 末端三肽以与 CVVM 的 C 末端三肽相似的方式与酶相互作用,这表明三肽包含用于底物识别的共同结构元件在四肽和五肽序列中。CMIIM 与 FTase 结合的分子动力学模拟进一步阐明了所涉及的分子相互作用,表明能够形成假定的催化有效 Zn(II)-硫醇物种。四肽 (CaaX 盒) 反应性的生物信息学预测与体内分析获得的五肽反应性很好地相关,这增强了 C 末端三肽基序的重要性。该分析为理解扩展的 CaaaX 盒基序的反应性提供了结构框架,并为预测具有 CaaaX 盒序列的其他 FTase 底物的反应性提供了一种可能有用的方法。