Maupin-Furlow J A, Aldrich H C, Ferry J G
Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park 16802-4500, USA.
J Bacteriol. 1998 Mar;180(6):1480-7. doi: 10.1128/JB.180.6.1480-1487.1998.
The 20S proteasome from the methanoarchaeon Methanosarcina thermophila was produced in Escherichia coli and characterized. The biochemical properties revealed novel features of the archaeal 20S proteasome. A fully active 20S proteasome could be assembled in vitro with purified native alpha ring structures and beta prosubunits independently produced in Escherichia coli, which demonstrated that accessory proteins are not essential for processing of the beta prosubunits or assembly of the 20S proteasome. A protein complex with a molecular mass intermediate to those of the alpha7 ring and the 20S proteasome was detected, suggesting that the 20S proteasome is assembled from precursor complexes. The heterologously produced M. thermophila 20S proteasome predominately catalyzed cleavage of peptide bonds carboxyl to the acidic residue Glu (postglutamyl activity) and the hydrophobic residues Phe and Tyr (chymotrypsinlike activity) in short chromogenic and fluorogenic peptides. Low-level hydrolyzing activities were also detected carboxyl to the acidic residue Asp and the basic residue Arg (trypsinlike activity). Sodium dodecyl sulfate and divalent or monovalent ions stimulated chymotrypsinlike activity and inhibited postglutamyl activity, whereas ATP stimulated postglutamyl activity but had little effect on the chymotrypsinlike activity. The results suggest that the 20S proteasome is a flexible protein which adjusts to binding of substrates. The 20S proteasome also hydrolyzed large proteins. Replacement of the nucleophilic Thr1 residue with an Ala in the beta subunit abolished all activities, which suggests that only one active site is responsible for the multisubstrate activity. Replacement of beta subunit active-site Lys33 with Arg reduced all activities, which further supports the existence of one catalytic site; however, this result also suggests a role for Lys33 in polarization of the Thr1 N, which serves to strip a proton from the active-site Thr1 Ogamma nucleophile. Replacement of Asp51 with Asn had no significant effect on trypsinlike activity, enhanced postglutamyl and trypsinlike activities, and only partially reduced lysozyme-hydrolyzing activity, which suggested that this residue is not essential for multisubstrate activity.
嗜热甲烷八叠球菌的20S蛋白酶体在大肠杆菌中产生并进行了表征。其生化特性揭示了古菌20S蛋白酶体的新特征。可以在体外将在大肠杆菌中独立产生的纯化天然α环结构和β前体亚基组装成完全活性的20S蛋白酶体,这表明辅助蛋白对于β前体亚基的加工或20S蛋白酶体的组装不是必需的。检测到一种分子量介于α7环和20S蛋白酶体之间的蛋白质复合物,这表明20S蛋白酶体是由前体复合物组装而成的。异源产生的嗜热甲烷八叠球菌20S蛋白酶体主要催化短生色和荧光肽中酸性残基Glu羧基侧的肽键裂解(谷氨酰胺后活性)以及疏水残基Phe和Tyr的肽键裂解(类胰凝乳蛋白酶活性)。在酸性残基Asp和碱性残基Arg的羧基侧也检测到低水平的水解活性(类胰蛋白酶活性)。十二烷基硫酸钠和二价或一价离子刺激类胰凝乳蛋白酶活性并抑制谷氨酰胺后活性,而ATP刺激谷氨酰胺后活性但对类胰凝乳蛋白酶活性影响很小。结果表明20S蛋白酶体是一种灵活的蛋白质,可适应底物的结合。20S蛋白酶体也能水解大蛋白。在β亚基中将亲核性的Thr1残基替换为Ala消除了所有活性,这表明只有一个活性位点负责多底物活性。将β亚基活性位点的Lys33替换为Arg降低了所有活性,这进一步支持了一个催化位点的存在;然而,该结果也表明Lys33在Thr1 N的极化中起作用,Thr1 N用于从活性位点的Thr1 Oγ亲核试剂上夺取一个质子。将Asp51替换为Asn对类胰蛋白酶活性没有显著影响,增强了谷氨酰胺后活性和类胰蛋白酶活性,并且仅部分降低了溶菌酶水解活性,这表明该残基对于多底物活性不是必需的。