Gangwar Shanti P, Meena Sita R, Saxena Ajay K
School of Life Sciences, Jawaharlal Nehru University, New Delhi 110 067, India.
Acta Crystallogr F Struct Biol Commun. 2014 Apr;70(Pt 4):433-7. doi: 10.1107/S2053230X14004166. Epub 2014 Mar 25.
The Mycobacterium tuberculosis ESX-1 secreted protein regulator (EspR, Rv3849) is the key protein that delivers bacterial proteins into the host cell during mycobacterial infection. EspR binds directly to the espACD operon and is involved in transcriptional activation. In the current study, M. tuberculosis EspR has been crystallized and its X-ray structure has been determined at 3.3 Å resolution in a P3221 crystal form. EspR forms a physiological dimer in the crystal. Each EspR monomer contains an N-terminal helix-turn-helix DNA-binding domain and a C-terminal dimerization domain. The EspR structure in the P3221 crystal form was compared with previously determined EspR structures in P32, P21 and P212121 crystal forms. Structural comparison analysis indicated that the N-terminal helix-turn-helix domain of EspR acquires a rigid structure in the four crystal forms. However, significant structural differences were observed in the C-terminal domain of EspR in the P21 crystal form when compared with the P3221 and P32 crystal forms. The interaction, stabilization energy and buried surface area analysis of EspR in the four different crystal forms have provided information about the physiological dimer interface of EspR.
结核分枝杆菌ESX-1分泌蛋白调节因子(EspR,Rv3849)是分枝杆菌感染期间将细菌蛋白递送至宿主细胞的关键蛋白。EspR直接与espACD操纵子结合并参与转录激活。在当前研究中,结核分枝杆菌EspR已结晶,并以P3221晶型在3.3 Å分辨率下确定了其X射线结构。EspR在晶体中形成生理性二聚体。每个EspR单体包含一个N端螺旋-转角-螺旋DNA结合结构域和一个C端二聚化结构域。将P3221晶型的EspR结构与先前确定的P32、P21和P212121晶型的EspR结构进行了比较。结构比较分析表明,EspR的N端螺旋-转角-螺旋结构域在四种晶型中获得了刚性结构。然而,与P3221和P32晶型相比,P21晶型的EspR C端结构域存在显著的结构差异。对四种不同晶型的EspR进行的相互作用、稳定能和掩埋表面积分析提供了有关EspR生理性二聚体界面的信息。