Wilson H L, Ou M S, Aldrich H C, Maupin-Furlow J
Department of Microbiology and Cell Science, University of Florida, Gainesville, Florida 32611-0700, USA.
J Bacteriol. 2000 Mar;182(6):1680-92. doi: 10.1128/JB.182.6.1680-1692.2000.
The 20S proteasome is a self-compartmentalized protease which degrades unfolded polypeptides and has been purified from eucaryotes, gram-positive actinomycetes, and archaea. Energy-dependent complexes, such as the 19S cap of the eucaryal 26S proteasome, are assumed to be responsible for the recognition and/or unfolding of substrate proteins which are then translocated into the central chamber of the 20S proteasome and hydrolyzed to polypeptide products of 3 to 30 residues. All archaeal genomes which have been sequenced are predicted to encode proteins with up to approximately 50% identity to the six ATPase subunits of the 19S cap. In this study, one of these archaeal homologs which has been named PAN for proteasome-activating nucleotidase was characterized from the hyperthermophile Methanococcus jannaschii. In addition, the M. jannaschii 20S proteasome was purified as a 700-kDa complex by in vitro assembly of the alpha and beta subunits and has an unusually high rate of peptide and unfolded-polypeptide hydrolysis at 100 degrees C. The 550-kDa PAN complex was required for CTP- or ATP-dependent degradation of beta-casein by archaeal 20S proteasomes. A 500-kDa complex of PAN(Delta1-73), which has a deletion of residues 1 to 73 of the deduced protein and disrupts the predicted N-terminal coiled-coil, also facilitated this energy-dependent proteolysis. However, this deletion increased the types of nucleotides hydrolyzed to include not only ATP and CTP but also ITP, GTP, TTP, and UTP. The temperature optimum for nucleotide (ATP) hydrolysis was reduced from 80 degrees C for the full-length protein to 65 degrees C for PAN(Delta1-73). Both PAN protein complexes were stable in the absence of ATP and were inhibited by N-ethylmaleimide and p-chloromercuriphenyl-sulfonic acid. Kinetic analysis reveals that the PAN protein has a relatively high V(max) for ATP and CTP hydrolysis of 3.5 and 5.8 micromol of P(i) per min per mg of protein as well as a relatively low affinity for CTP and ATP with K(m) values of 307 and 497 microM compared to other proteins of the AAA family. Based on electron micrographs, PAN and PAN(Delta1-73) apparently associate with the ends of the 20S proteasome cylinder. These results suggest that the M. jannaschii as well as related archaeal 20S proteasomes require a nucleotidase complex such as PAN to mediate the energy-dependent hydrolysis of folded-substrate proteins and that the N-terminal 73 amino acid residues of PAN are not absolutely required for this reaction.
20S蛋白酶体是一种自我分隔的蛋白酶,可降解未折叠的多肽,已从真核生物、革兰氏阳性放线菌和古细菌中纯化得到。能量依赖复合物,如真核生物26S蛋白酶体的19S帽,被认为负责底物蛋白的识别和/或展开,然后底物蛋白被转运到20S蛋白酶体的中央腔室并水解为3至30个残基的多肽产物。所有已测序的古细菌基因组预计编码与19S帽的六个ATP酶亚基具有高达约50%同一性的蛋白质。在本研究中,从嗜热栖热甲烷球菌中鉴定了一种古细菌同源物,它被命名为蛋白酶体激活核苷酸酶(PAN)。此外,通过α和β亚基的体外组装,将嗜热栖热甲烷球菌20S蛋白酶体纯化为700 kDa的复合物,并且在100℃下具有异常高的肽和未折叠多肽水解速率。古细菌20S蛋白酶体对β-酪蛋白进行CTP或ATP依赖性降解需要550 kDa的PAN复合物。PAN(Delta1-73)的500 kDa复合物缺失了推导蛋白的1至73位残基并破坏了预测的N端卷曲螺旋,它也促进了这种能量依赖性蛋白水解。然而,这种缺失增加了水解的核苷酸类型,不仅包括ATP和CTP,还包括ITP、GTP、TTP和UTP。核苷酸(ATP)水解的最适温度从全长蛋白的80℃降至PAN(Delta1-73)的65℃。两种PAN蛋白复合物在没有ATP的情况下都很稳定,并被N-乙基马来酰亚胺和对氯汞苯磺酸抑制。动力学分析表明,PAN蛋白对ATP和CTP水解的V(max)相对较高,分别为每毫克蛋白每分钟3.5和5.8微摩尔无机磷酸,并且与AAA家族的其他蛋白相比,对CTP和ATP的亲和力相对较低,K(m)值分别为307和497 microM。基于电子显微镜照片,PAN和PAN(Delta1-73)显然与20S蛋白酶体圆柱体的末端相关联。这些结果表明,嗜热栖热甲烷球菌以及相关的古细菌20S蛋白酶体需要一种核苷酸酶复合物,如PAN,来介导折叠底物蛋白的能量依赖性水解,并且PAN的N端73个氨基酸残基对于该反应不是绝对必需的。