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1
Identification of a 123-kilodalton protein (Gli123) involved in machinery for gliding motility of Mycoplasma mobile.鉴定一种参与运动支原体滑行运动机制的123千道尔顿蛋白质(Gli123)。
J Bacteriol. 2005 Aug;187(16):5578-84. doi: 10.1128/JB.187.16.5578-5584.2005.
2
Identification of a 521-kilodalton protein (Gli521) involved in force generation or force transmission for Mycoplasma mobile gliding.鉴定一种参与运动支原体滑行力产生或力传递的521千道尔顿蛋白质(Gli521)。
J Bacteriol. 2005 May;187(10):3502-10. doi: 10.1128/JB.187.10.3502-3510.2005.
3
Identification of a 349-kilodalton protein (Gli349) responsible for cytadherence and glass binding during gliding of Mycoplasma mobile.鉴定一种负责运动支原体滑行过程中细胞黏附和玻璃黏附的349千道尔顿蛋白(Gli349)。
J Bacteriol. 2004 Mar;186(5):1537-45. doi: 10.1128/JB.186.5.1537-1545.2004.
4
Structure and Function of Gli123 Involved in Mycoplasma mobile Gliding.参与黏支原体滑动的 Gli123 的结构与功能。
J Bacteriol. 2023 Mar 21;205(3):e0034022. doi: 10.1128/jb.00340-22. Epub 2023 Feb 7.
5
Regions on Gli349 and Gli521 protein molecules directly involved in movements of Mycoplasma mobile gliding machinery, suggested by use of inhibitory antibodies and mutants.通过使用抑制性抗体和突变体表明,Gli349和Gli521蛋白质分子上直接参与运动支原体滑行机制运动的区域。
J Bacteriol. 2009 Mar;191(6):1982-5. doi: 10.1128/JB.01012-08. Epub 2009 Jan 5.
6
Identification of a novel nucleoside triphosphatase from Mycoplasma mobile: a prime candidate motor for gliding motility.从运动支原体中鉴定出一种新型核苷三磷酸酶:滑行运动的主要候选动力蛋白。
Biochem J. 2007 Apr 1;403(1):71-7. doi: 10.1042/BJ20061439.
7
Cell surface differentiation of Mycoplasma mobile visualized by surface protein localization.通过表面蛋白定位观察运动支原体的细胞表面分化
Microbiology (Reading). 2004 Dec;150(Pt 12):4001-8. doi: 10.1099/mic.0.27436-0.
8
Detection of Steps and Rotation in the Gliding Motility of Mycoplasma mobile.滑行运动中支原体的步伐和旋转检测。
Methods Mol Biol. 2023;2646:327-336. doi: 10.1007/978-1-0716-3060-0_27.
9
Triskelion structure of the Gli521 protein, involved in the gliding mechanism of Mycoplasma mobile.Gli521 蛋白的三螺旋束结构,参与黏附运动型支原体的滑行机制。
J Bacteriol. 2010 Feb;192(3):636-42. doi: 10.1128/JB.01143-09. Epub 2009 Nov 13.
10
Cytoskeletal "jellyfish" structure of Mycoplasma mobile.运动支原体的细胞骨架“水母”结构
Proc Natl Acad Sci U S A. 2007 Dec 4;104(49):19518-23. doi: 10.1073/pnas.0704280104. Epub 2007 Nov 27.

引用本文的文献

1
Gliding direction of correlates with the curved configuration of its cell shape.……的滑动方向与其细胞形状的弯曲形态相关。 (原文中“Gliding direction of ”这里少了具体所指内容)
Biophys Physicobiol. 2025 Feb 26;22(1):e220006. doi: 10.2142/biophysico.bppb-v22.0006. eCollection 2025.
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Nano-Scale Video Imaging of Motility Machinery by High-Speed Atomic Force Microscopy.利用高速原子力显微镜对运动机制进行纳米级视频成像。
Biomolecules. 2025 Feb 10;15(2):257. doi: 10.3390/biom15020257.
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Internal structure of gliding machinery analyzed by negative staining electron tomography.通过负染色电子断层扫描分析滑动机械的内部结构。
Biophys Physicobiol. 2024 May 28;21(2):e210015. doi: 10.2142/biophysico.bppb-v21.0015. eCollection 2024.
4
Detection of Steps and Rotation in the Gliding Motility of Mycoplasma mobile.滑行运动中支原体的步伐和旋转检测。
Methods Mol Biol. 2023;2646:327-336. doi: 10.1007/978-1-0716-3060-0_27.
5
Structure and Function of Gli123 Involved in Mycoplasma mobile Gliding.参与黏支原体滑动的 Gli123 的结构与功能。
J Bacteriol. 2023 Mar 21;205(3):e0034022. doi: 10.1128/jb.00340-22. Epub 2023 Feb 7.
6
Chained Structure of Dimeric F-like ATPase in Mycoplasma mobile Gliding Machinery.二聚 F 型 ATP 酶在黏体支原体滑行机制中的链式结构。
mBio. 2021 Aug 31;12(4):e0141421. doi: 10.1128/mBio.01414-21. Epub 2021 Jul 20.
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Movements of Mycoplasma mobile Gliding Machinery Detected by High-Speed Atomic Force Microscopy.高速原子力显微镜检测到移行支原体滑行机制的运动。
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8
Exploring Biology: Opportunities and Challenges.探索生物学:机遇与挑战。
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9
Identification and sequence analyses of the gliding machinery proteins from Mycoplasma mobile.滑行机制蛋白的鉴定与序列分析来自运动支原体。
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10
Refined Mechanism of Mycoplasma mobile Gliding Based on Structure, ATPase Activity, and Sialic Acid Binding of Machinery.基于结构、ATP 酶活性和机械结合唾液酸的研究,解析黏细菌滑动的精细机制
mBio. 2019 Dec 24;10(6):e02846-19. doi: 10.1128/mBio.02846-19.

本文引用的文献

1
Sequence analysis of the gliding protein Gli349 in .. 中滑行蛋白Gli349的序列分析
Biophysics (Nagoya-shi). 2005 May 25;1:33-43. doi: 10.2142/biophysics.1.33. eCollection 2005.
2
Identification of a 521-kilodalton protein (Gli521) involved in force generation or force transmission for Mycoplasma mobile gliding.鉴定一种参与运动支原体滑行力产生或力传递的521千道尔顿蛋白质(Gli521)。
J Bacteriol. 2005 May;187(10):3502-10. doi: 10.1128/JB.187.10.3502-3510.2005.
3
Living microtransporter by uni-directional gliding of Mycoplasma along microtracks.通过支原体沿微轨道单向滑行实现的活体微型运输器。
Biochem Biophys Res Commun. 2005 May 27;331(1):318-24. doi: 10.1016/j.bbrc.2005.03.168.
4
Involvement of P1 adhesin in gliding motility of Mycoplasma pneumoniae as revealed by the inhibitory effects of antibody under optimized gliding conditions.在优化的滑行条件下,抗体的抑制作用揭示了P1黏附素参与肺炎支原体的滑行运动。
J Bacteriol. 2005 Mar;187(5):1875-7. doi: 10.1128/JB.187.5.1875-1877.2005.
5
Cell surface differentiation of Mycoplasma mobile visualized by surface protein localization.通过表面蛋白定位观察运动支原体的细胞表面分化
Microbiology (Reading). 2004 Dec;150(Pt 12):4001-8. doi: 10.1099/mic.0.27436-0.
6
HMW1 is required for stability and localization of HMW2 to the attachment organelle of Mycoplasma pneumoniae.高分子量蛋白1(HMW1)是肺炎支原体的高分子量蛋白2(HMW2)定位于附着细胞器并保持稳定所必需的。
J Bacteriol. 2004 Dec;186(24):8221-8. doi: 10.1128/JB.186.24.8221-8228.2004.
7
Use of fluorescent-protein tagging to determine the subcellular localization of mycoplasma pneumoniae proteins encoded by the cytadherence regulatory locus.利用荧光蛋白标记法确定由黏附调节基因座编码的肺炎支原体蛋白的亚细胞定位。
J Bacteriol. 2004 Oct;186(20):6944-55. doi: 10.1128/JB.186.20.6944-6955.2004.
8
The complete genome and proteome of Mycoplasma mobile.运动支原体的全基因组和蛋白质组
Genome Res. 2004 Aug;14(8):1447-61. doi: 10.1101/gr.2674004.
9
Spike structure at the interface between gliding Mycoplasma mobile cells and glass surfaces visualized by rapid-freeze-and-fracture electron microscopy.通过快速冷冻断裂电子显微镜观察到的滑行运动的运动支原体细胞与玻璃表面界面处的刺突结构。
J Bacteriol. 2004 Jul;186(13):4382-6. doi: 10.1128/JB.186.13.4382-4386.2004.
10
Energetics of gliding motility in Mycoplasma mobile.运动支原体滑行运动的能量学
J Bacteriol. 2004 Jul;186(13):4254-61. doi: 10.1128/JB.186.13.4254-4261.2004.

鉴定一种参与运动支原体滑行运动机制的123千道尔顿蛋白质(Gli123)。

Identification of a 123-kilodalton protein (Gli123) involved in machinery for gliding motility of Mycoplasma mobile.

作者信息

Uenoyama Atsuko, Miyata Makoto

机构信息

Department of Biology, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan.

出版信息

J Bacteriol. 2005 Aug;187(16):5578-84. doi: 10.1128/JB.187.16.5578-5584.2005.

DOI:10.1128/JB.187.16.5578-5584.2005
PMID:16077102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1196088/
Abstract

Mycoplasma mobile glides on a glass surface in the direction of its tapered end by an unknown mechanism. Two large proteins, Gli349 and Gli521, were recently reported to be involved in glass binding and force generation/transmission, respectively, in M. mobile gliding. These proteins are coded tandemly with two other open reading frames (ORFs) in the order p123-gli349-gli521-p42 on the genome. In the present study, reverse transcriptase PCR analysis suggested that these four ORFs are transcribed cistronically. To characterize the p123 gene coding a 123-kDa protein (Gli123) of 1,128 amino acids, we raised polyclonal antibody against the Gli123 protein. Immunoblotting for Gli123 revealed that Gli123 was missing in a mutant strain, m12, which was previously isolated and characterized by a deficiency in glass binding. Sequencing analysis showed a nonsense mutation at the 523rd amino acid of the protein in the m12 mutant. Immunofluorescence microscopy with the polyclonal antibody showed that Gli123 is localized at the head-like protrusion's base, the cell neck, which is specialized for gliding, as observed for Gli349 and Gli521. Localization of the gliding proteins, Gli349 and Gli521, was disturbed in the m12 mutant, suggesting that Gli123 is essential for the positioning of gliding proteins in the cell neck.

摘要

移动支原体通过未知机制在玻璃表面朝着其锥形末端滑行。最近有报道称,两种大蛋白Gli349和Gli521分别参与移动支原体滑行过程中的玻璃结合以及力的产生/传递。这些蛋白在基因组上与另外两个开放阅读框(ORF)串联编码,顺序为p123 - gli349 - gli521 - p42。在本研究中,逆转录酶PCR分析表明这四个ORF是顺反子转录的。为了表征编码1128个氨基酸的123 kDa蛋白(Gli123)的p123基因,我们制备了针对Gli123蛋白的多克隆抗体。对Gli123的免疫印迹分析显示,在先前分离并鉴定为缺乏玻璃结合能力的突变株m12中,Gli123缺失。测序分析表明,m12突变体中该蛋白的第523个氨基酸处存在无义突变。用多克隆抗体进行的免疫荧光显微镜检查显示,Gli123定位于头部样突起的基部,即细胞颈部,这是专门用于滑行的部位,就像Gli349和Gli521的情况一样。在m12突变体中,滑行蛋白Gli349和Gli521的定位受到干扰,这表明Gli123对于滑行蛋白在细胞颈部的定位至关重要。