Baker Rosanna P, Young Keith, Feng Liang, Shi Yigong, Urban Sinisa
Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, 507 Preclinical Teaching Building, 725 North Wolfe Street, Baltimore, MD 21205, USA.
Proc Natl Acad Sci U S A. 2007 May 15;104(20):8257-62. doi: 10.1073/pnas.0700814104. Epub 2007 Apr 26.
Intramembrane proteolysis is a core regulatory mechanism of cells that raises a biochemical paradox of how hydrolysis of peptide bonds is accomplished within the normally hydrophobic environment of the membrane. Recent high-resolution crystal structures have revealed that rhomboid proteases contain a catalytic serine recessed into the plane of the membrane, within a hydrophilic cavity that opens to the extracellular face, but protected laterally from membrane lipids by a ring of transmembrane segments. This architecture poses questions about how substrates enter the internal active site laterally from membrane lipid. Because structures are static glimpses of a dynamic enzyme, we have taken a structure-function approach analyzing >40 engineered variants to identify the gating mechanism used by rhomboid proteases. Importantly, our analyses were conducted with a substrate that we show is cleaved at two intramembrane sites within the previously defined Spitz substrate motif. Engineered mutants in the L1 loop and active-site region of the GlpG rhomboid protease suggest an important structural, rather than dynamic, gating function for the L1 loop that was first proposed to be the substrate gate. Conversely, three classes of mutations that promote transmembrane helix 5 displacement away from the protease core dramatically enhanced enzyme activity 4- to 10-fold. Our functional analyses have identified transmembrane helix 5 movement to gate lateral substrate entry as a rate-limiting step in intramembrane proteolysis. Moreover, our mutagenesis also underscores the importance of other residue interactions within the enzyme that warrant further scrutiny.
膜内蛋白水解是细胞的一种核心调节机制,它引发了一个生化悖论,即在膜通常的疏水环境中,肽键的水解是如何完成的。最近的高分辨率晶体结构显示,类菱形蛋白酶含有一个催化丝氨酸,该丝氨酸凹陷在膜平面内,位于一个通向细胞外表面的亲水腔内,但通过一圈跨膜片段在侧面免受膜脂的影响。这种结构引发了关于底物如何从膜脂侧向进入内部活性位点的问题。由于结构是动态酶的静态快照,我们采用了结构-功能方法,分析了40多个工程变体,以确定类菱形蛋白酶使用的门控机制。重要的是,我们的分析是使用一种底物进行的,我们发现该底物在先前定义的Spitz底物基序内的两个膜内位点被切割。GlpG类菱形蛋白酶L1环和活性位点区域的工程突变体表明,L1环具有重要的结构而非动态门控功能,L1环最初被认为是底物门。相反,三类促进跨膜螺旋5从蛋白酶核心移位的突变显著增强了酶活性4至10倍。我们的功能分析确定跨膜螺旋5的移动以控制侧向底物进入是膜内蛋白水解的限速步骤。此外,我们的诱变还强调了酶内其他残基相互作用的重要性,值得进一步研究。