Structural Biology and Bioinformatics Division, Indian Institute of Chemical Biology, 4 Raja S.C. Mullick Road, Kolkata 700032, West Bengal, India.
Protein J. 2012 Aug;31(6):487-98. doi: 10.1007/s10930-012-9426-5.
YspC is an annotated translocator of Yersinia secretion apparatus-Yersinia secretion protein type three secretion system of Yersinia enterocolitica, it forms an 1:1 complex with its cognate chaperone SycB. Unlike other translocators, YspC is highly soluble inspite of having a transmembrane region. Size exclusion chromatography shows that YspC exists predominantly in a monomeric form. Multiple sequence alignment and ConSurf (a web based bioinformatic tool) analysis confirm its significant deviation from the closest class of minor translocators. YspC also possesses a tertiary structure signal seen from near UV CD, further confirming its unique nature amongst the groups of translocators. Far UV CD depicts that YspC is predominantly an α-helical protein; however, its secondary structure alters in the YspC-SycB complex. Thermal denaturation curve predicts a cooperative melting behaviour for YspC which is altered in the YspC-SycB complex. Furthermore, trypsinolysis data confirms a different digestion pattern for YspC in isolation, when compared to the complex form with SycB. From the Forsters resonance energy transfer analysis, it can be predicted that the two tetratricopeptide repeat regions of SycB are masked while it forms a complex with YspC and this is further confirmed by the interaction studies of YspC with two truncated forms of SycB. YspC interacted with ∆SycB₁₋₁₁₄ and ∆SycB₃₆₋₁₁₄ (possessing only the two TPR regions). However, the complexes formed between YspC and truncated forms of SycB have altered physiological states.
YspC 是耶尔森氏菌分泌装置-Yersinia 分泌蛋白三型分泌系统的注释转运蛋白,它与同源伴侣蛋白 SycB 形成 1:1 复合物。与其他转运蛋白不同,YspC 尽管具有跨膜区域,但仍具有很高的可溶性。尺寸排阻层析表明,YspC 主要以单体形式存在。多序列比对和 ConSurf(一种基于网络的生物信息学工具)分析证实,它与最接近的次要转运蛋白类群存在显著偏差。YspC 还具有从近紫外线 CD 看到的三级结构信号,进一步证实了它在转运蛋白组中的独特性质。远紫外线 CD 描绘了 YspC 主要是一种α-螺旋蛋白;然而,在 YspC-SycB 复合物中,其二级结构发生了变化。热变性曲线预测 YspC 具有协同熔融行为,而在 YspC-SycB 复合物中则发生了改变。此外,胰蛋白酶水解数据证实 YspC 在分离状态下的消化模式与与 SycB 形成复合物时不同。从 Forsters 共振能量转移分析可以预测,当 SycB 与 YspC 形成复合物时,其两个四肽重复区域被掩盖,这进一步通过 YspC 与 SycB 的两个截断形式的相互作用研究得到证实。YspC 与 ∆SycB₁₋₁₁₄ 和 ∆SycB₃₆₋₁₁₄(仅具有两个 TPR 区域)相互作用。然而,YspC 与截断形式的 SycB 形成的复合物具有改变的生理状态。