Sabljić Igor, Tomin Marko, Matovina Mihaela, Sučec Iva, Tomašić Paić Ana, Tomić Antonija, Abramić Marija, Tomić Sanja
Division of Physical Chemistry, Ruđer Bošković Institute, Zagreb, Croatia.
Division of Organic Chemistry and Biochemistry, Ruđer Bošković Institute, Zagreb, Croatia.
PLoS One. 2018 Feb 8;13(2):e0192488. doi: 10.1371/journal.pone.0192488. eCollection 2018.
Dipeptidyl peptidase III (DPP III) isolated from the thermophilic bacteria Caldithrix abyssi (Ca) is a two-domain zinc exopeptidase, a member of the M49 family. Like other DPPs III, it cleaves dipeptides from the N-terminus of its substrates but differently from human, yeast and Bacteroides thetaiotaomicron (mesophile) orthologs, it has the pentapeptide zinc binding motif (HEISH) in the active site instead of the hexapeptide (HEXXGH). The aim of our study was to investigate structure, dynamics and activity of CaDPP III, as well as to find possible differences with already characterized DPPs III from mesophiles, especially B. thetaiotaomicron. The enzyme structure was determined by X-ray diffraction, while stability and flexibility were investigated using MD simulations. Using molecular modeling approach we determined the way of ligands binding into the enzyme active site and identified the possible reasons for the decreased substrate specificity compared to other DPPs III. The obtained results gave us possible explanation for higher stability, as well as higher temperature optimum of CaDPP III. The structural features explaining its altered substrate specificity are also given. The possible structural and catalytic significance of the HEISH motive, unique to CaDPP III, was studied computationally, comparing the results of long MD simulations of the wild type enzyme with those obtained for the HEISGH mutant. This study presents the first structural and biochemical characterization of DPP III from a thermophile.
从嗜热细菌深渊热丝菌(Ca)中分离出的二肽基肽酶III(DPP III)是一种双结构域锌外肽酶,属于M49家族。与其他DPP III一样,它从底物的N端切割二肽,但与人类、酵母和嗜温的多形拟杆菌直系同源物不同的是,它在活性位点具有五肽锌结合基序(HEISH),而非六肽(HEXXGH)。我们研究的目的是探究深渊热丝菌DPP III的结构、动力学和活性,以及找出与已表征的嗜温菌DPP III(尤其是多形拟杆菌)可能存在的差异。通过X射线衍射确定了该酶的结构,同时使用分子动力学模拟研究了其稳定性和灵活性。我们采用分子建模方法确定了配体结合到酶活性位点的方式,并确定了与其他DPP III相比底物特异性降低的可能原因。所得结果为深渊热丝菌DPP III更高的稳定性以及更高的最适温度提供了可能的解释。还给出了解释其底物特异性改变的结构特征。通过计算研究了深渊热丝菌DPP III特有的HEISH基序可能具有的结构和催化意义,将野生型酶的长时间分子动力学模拟结果与HEISGH突变体的结果进行了比较。本研究首次对嗜热菌的DPP III进行了结构和生化表征。