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人髓系细胞触发受体-1模拟多肽的筛选和鉴定 被引量:3

Screening and identification of human triggering receptor expressed on myeloid cells-1 mimetic peptides
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摘要 目的寻找能特异性与人髓系细胞触发受体-1(TREM-1)蛋白结合并抑制其传导通路的多肽。方法克隆、表达和纯化TREM-1功能区蛋白,并以之为诱饵蛋白,筛选随机噬菌体展示肽库。经过4轮生物淘洗,通过ELISA方法和单核细胞ELISA方法分析噬菌体克隆与TREM-1蛋白的亲和力。化学合成模拟多肽,检测其对盲肠结扎穿刺(CLP)小鼠的治疗效果。结果成功找到5种噬菌体克隆,ELISA法和细胞ELISA均阳性。应用化学方法合成的模拟多肽HYGMTHPNTMSH能降低CLP小鼠的死亡率。结论模拟多肽HYGMTHPNTMSH对脓毒症小鼠有保护作用。 Objective To find mimetic peptides which bind specifically with triggering receptor expressed on myeloid cells-1 (TREM-1) and inhibit the TREM-1 pathway. Methods The functioning region of TREM-1 protein was cloned, expressed and purified. With the recombinant protein of TREM-1 as the target molecule, the mimetic peptides were screened from a random phage display peptide library. Four rounds of biopanning were carried out, and enzyme linked immunosorbent assay (ELISA) and monocyte cell ELISA were used to evaluate the binding between the phage clone and TREM-h Then, chemical synthesis of the mimetic peptide was carried out, and its therapeutic effect on cecal ligation and puncture (CLP) in mice was investigated. Results Five phage clones from the fourth round of biopanning were selected at random, all of them were positive in sandwich ELISA and monocyte cell ELISA. Administration of the chemically synthesized mimetic peptide HYGMTHPNTMSH reduced the mortality of CLP mice. Conclusion Mimetic peptide HYGMTHPNTMSH can protect the mice wtih sepsis from death.
出处 《中华老年多器官疾病杂志》 2008年第6期506-510,共5页 Chinese Journal of Multiple Organ Diseases in the Elderly
基金 广东省自然科学基金资助课题(资助号:06022087)
关键词 髓系细胞触发受体-1 模拟多肽 筛选随机噬菌体展示肽库 triggering receptor expressed on myeloid cells-1 mimetic peptide screening random phage display peptide library
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  • 1[1]Cohen J.The immunopathogenesis of sepsis.Nature,2002,420:885-891.
  • 2[2]Bouchon A,Dietrich J,Colonna M.Cutting edge:inflammatory responses can be triggered by TREM-1,a novel receptor expressed on neutrophils and monocytes.J Immunol,2000,164:4991-4995.
  • 3[3]Bouchon A,Facchetti F,Weigand MA,et al.TREM-1 amplifies inflammation and is a crucial mediator of septic shock.Nature,2001,410:1103-1107.
  • 4[4]Fortin CF,Lesur O,Fulop TJ.Effects of TREM-1 activation in human neutrophils:activation of signaling pathways,recruitment into lipid rafts and association with TLR4.Int Immunol,2007,19:41-50.
  • 5[5]Radaev S,Kattah M,Rostro B,et al.Crystal structure of the human myeloid cell activating receptor TREM-1.Structure,2003,11:1527-1535.
  • 6[6]Kelker MS,Foss TR,Peti W,et al.Crystal structure of human triggering receptor expressed on myeloid cells 1 (TREM-1) at 1.47 A.J Mol Biol,2004,342:1237-1248.
  • 7[7]Carson M,Johnson DH,McDonald H,et al.His-tag impact on structure.Acta Crystallogr D Biol Crystallogr,2007,63(Pt 3):295-301.
  • 8[8]Cheadle C,Ivashchenko Y,South V,et al.Identification of a Src SH3 domain binding motif by screening a random phage display library.J Biol Chem,1994,269:24034-24039.
  • 9[9]Stockman BJ,Bannow CA,Miceli RM,et al.Chemical shift differences between free and Fab-bound peptide correlate with a two-stage selection of peptide sequences from a random phage display library to delineate critical and non-critical residues for antibody recognition.Int J Pept Protein Res,1995,45:11-16.
  • 10[10]Mahdy AM,Lowes DA,Galley HF,et al.Production of soluble triggering receptor expressed on myeloid cells by lipopolysaccharide-stimulated human neutrophils involves de novo protein synthesis.Clin Vaccine Immunol,2006,13:492-495.

同被引文献38

  • 1Kelker MS, Foss TR, Peti W, et al. Crystal structure of human triggering receptor expressed on myeloid cells 1 (TREM 1) at 1.47 A. J Mol Biol,2004,342:1237-1248.
  • 2Gibot S,Kolopp Sarda MN,Bene MC,et al. A soluble form of the triggering receptor expressed on myeloid cells-1 modulates the inflammatory response in murine sepsis. J Exp Med, 2004,200 : 1419-1426.
  • 3Gibot S, Buonsanti C, Massin F, et al. Modulation of the triggering receptor expressed on the myeloid cell type 1 pathway in murine septic shock. Infect Immun, 2006, 74: 2823-2830.
  • 4Ornatowska M,Azim AC,Wang X,et al. Functional genomics of silencing TREM-1 on TLR4 signaling in macrophages. Am J Physiol Lung Cell Mol Physiol,2007,293:L1377-L1384.
  • 5Dower K ,Ellis DK ,Saraf K ,et al. Innate immune responses to TREM-1 activation: overlap, divergence, and positive and negative cross-talk with bacterial lipopolysaeeharide. J Immunol, 2008,180 : 3520 3534.
  • 6Zeng H.Ornatowska M,Joo MS,et al. TREM-1 expression in maerophages is regulated at transcriptional level by NF-kappa B and PU. 1. Eur J Immunol,2007,37:2300-2308.
  • 7Tejera A, Santolaria F, Diez ML, et al. Prognosis of community acquired pneumonia (CAP):value of triggering receptor expressed on myeloid cells-1 (TREM-1) and other mediators of the inflammatory response. Cytokine, 2007,38: 117-123.
  • 8Murakami Y, Kohsaka Lipopolysaccharide-ind uced H, Kitasato H, et al. up-regulation of triggering receptor expressed on myeloid cells-1 expression on maerophages is regulated by endogenous prostaglandin E2. J Immunol, 2007,178 : 1144-1150.
  • 9Gibot S, Massin F, Le Renard P, et al. Surface and soluble triggering receptor expressed on myeloid cells-1: expression patterns in murine sepsis. Crit Care Med. 2005, 33: 1787- 1793.
  • 10Nguyen HB,Rivers EP, Abrahamian FM,et al. Severe sepsis and septic shock: review of the literature and emergency department management guidelines. Ann Emerg Med, 2006, 48:28-54.

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