Department of Microbiology and Immunology, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr, San Antonio, TX 78229, USA.
Cell Microbiol. 2010 Dec;12(12):1821-31. doi: 10.1111/j.1462-5822.2010.01513.x.
We identified Mpn133 as a Ca(2+)-dependent cytotoxic nuclease of Mycoplasma pneumoniae. Flow cytometry analysis and immunofluorescence studies revealed the binding and internalization of recombinant Mpn133 (rMpn133) in human airway A549 cells. Amino acid sequence comparisons of Mpn133 with other mycoplasma nucleases demonstrated the presence of a unique glutamic acid-, lysine- and serine-rich region (EKS region; amino acids 72-110). Deletion of this EKS peptide (rMpn133(Δ72-110)) abrogated its binding and internalization but not its nuclease activity. The function of the EKS region in host cell trafficking and nuclear localization was reinforced by the successful delivery of EKS-conjugated mCherry protein into A549 cells. rMpn133, but not rMpn133(Δ72-110), induced apoptosis-like death in A549 cells. This observation suggested a unique role of Mpn133 as an important contributor to M. pneumoniae-associated life cycle events and as a virulence factor in host-associated cytopathologies. In addition, the distinct property of the EKS peptide in delivery of proteins, like mCherry, into target cells opens new avenues to the establishment of novel concepts of drug delivery and therapy.
我们鉴定出 Mpn133 是肺炎支原体的一种依赖 Ca(2+)的细胞毒性核酸内切酶。流式细胞术分析和免疫荧光研究显示重组 Mpn133(rMpn133)与人气道 A549 细胞的结合和内化。Mpn133 与其他支原体核酸酶的氨基酸序列比较表明存在独特的谷氨酸、赖氨酸和丝氨酸丰富区域(EKS 区域;氨基酸 72-110)。该 EKS 肽(rMpn133(Δ72-110))缺失会破坏其结合和内化,但不影响其核酸酶活性。EKS 区域在宿主细胞运输和核定位中的功能通过成功将 EKS 缀合的 mCherry 蛋白递送至 A549 细胞得到了加强。rMpn133 而非 rMpn133(Δ72-110),诱导 A549 细胞发生类似凋亡的死亡。这一观察结果表明 Mpn133 具有独特的作用,是肺炎支原体相关生命周期事件的重要贡献者,也是宿主相关细胞病变中的毒力因子。此外,EKS 肽在将 mCherry 等蛋白递送至靶细胞中的独特特性为建立新型药物递送和治疗概念开辟了新途径。