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相似文献

1
Phage-displayed peptide libraries.噬菌体展示肽库
Curr Opin Biotechnol. 1998 Aug;9(4):427-36. doi: 10.1016/s0958-1669(98)80017-7.
2
Display technologies expand their horizons.
Trends Biotechnol. 1999 Apr;17(4):137-8. doi: 10.1016/s0167-7799(98)01289-x.
3
Recent advances in phage display.噬菌体展示技术的最新进展。
Curr Opin Biotechnol. 1993 Oct;4(5):526-30. doi: 10.1016/0958-1669(93)90072-5.
4
Selection of phage displayed peptides from a random 10-mer library recognising a peptide target.从识别肽靶标的随机十肽文库中筛选噬菌体展示肽。
Immunotechnology. 1998 Jun;4(1):21-8. doi: 10.1016/s1380-2933(98)00008-6.
5
Designing scaffolds of peptides for phage display libraries.用于噬菌体展示文库的肽支架设计。
J Biosci Bioeng. 2005 May;99(5):448-56. doi: 10.1263/jbb.99.448.
6
Phage display technology: clinical applications and recent innovations.噬菌体展示技术:临床应用与最新创新
Clin Biochem. 2002 Sep;35(6):425-45. doi: 10.1016/s0009-9120(02)00343-0.
7
Using phage as a platform to select cancer cell-targeting peptides.利用噬菌体作为平台筛选癌细胞靶向肽。
Methods Mol Biol. 2014;1108:57-68. doi: 10.1007/978-1-62703-751-8_4.
8
Phage display of proteins.蛋白质的噬菌体展示
Curr Opin Biotechnol. 1996 Oct;7(5):547-53. doi: 10.1016/s0958-1669(96)80060-7.
9
Peptide display on filamentous phage capsids. A new powerful tool to study protein-ligand interaction.
FEBS Lett. 1992 Jul 27;307(1):66-70. doi: 10.1016/0014-5793(92)80903-t.
10
Selectively infective phage (SIP) technology: a novel method for in vivo selection of interacting protein-ligand pairs.选择性感染噬菌体(SIP)技术:一种体内筛选相互作用蛋白-配体对的新方法。
Nat Med. 1997 Jun;3(6):694-6. doi: 10.1038/nm0697-694.

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Discovery of Cyclic Peptide Binders from Chemically Constrained Yeast Display Libraries.从化学约束酵母展示文库中发现环肽结合物。
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Selection and identification of novel peptides specifically targeting human cervical cancer.新型人宫颈癌靶向肽的筛选与鉴定。
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Beyond Helper Phage: Using "Helper Cells" to Select Peptide Affinity Ligands.超越辅助噬菌体:利用“辅助细胞”筛选肽亲和配体。
PLoS One. 2016 Sep 14;11(9):e0160940. doi: 10.1371/journal.pone.0160940. eCollection 2016.
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Exploring the Secretomes of Microbes and Microbial Communities Using Filamentous Phage Display.利用丝状噬菌体展示技术探索微生物及微生物群落的分泌蛋白组
Front Microbiol. 2016 Apr 7;7:429. doi: 10.3389/fmicb.2016.00429. eCollection 2016.
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Ff-nano, short functionalized nanorods derived from Ff (f1, fd, or M13) filamentous bacteriophage.Ff-纳米颗粒,即源自Ff(f1、fd或M13)丝状噬菌体的短功能化纳米棒。
Front Microbiol. 2015 Apr 20;6:316. doi: 10.3389/fmicb.2015.00316. eCollection 2015.
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Metasecretome-selective phage display approach for mining the functional potential of a rumen microbial community.用于挖掘瘤胃微生物群落功能潜力的元分泌组选择性噬菌体展示方法。
BMC Genomics. 2014 May 12;15(1):356. doi: 10.1186/1471-2164-15-356.
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Class A β-lactamases as versatile scaffolds to create hybrid enzymes: applications from basic research to medicine.A 类 β-内酰胺酶作为多功能支架构建杂合酶:从基础研究到医学的应用。
Biomed Res Int. 2013;2013:827621. doi: 10.1155/2013/827621. Epub 2013 Aug 28.
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Unique secreted-surface protein complex of Lactobacillus rhamnosus, identified by phage display.鼠李糖乳杆菌独特的分泌表面蛋白复合物,通过噬菌体展示技术鉴定。
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A peptide that binds specifically to the β-amyloid of Alzheimer's disease: selection and assessment of anti-β-amyloid neurotoxic effects.一种能与阿尔茨海默病β-淀粉样蛋白特异性结合的肽:抗β-淀粉样蛋白神经毒性作用的选择和评估。
PLoS One. 2011;6(11):e27649. doi: 10.1371/journal.pone.0027649. Epub 2011 Nov 10.
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Screening random peptide libraries with subacute sclerosing panencephalitis brain-derived recombinant antibodies identifies multiple epitopes in the C-terminal region of the measles virus nucleocapsid protein.用亚急性硬化性全脑炎脑源性重组抗体筛选随机肽库可鉴定麻疹病毒核衣壳蛋白C末端区域的多个表位。
J Virol. 2006 Dec;80(24):12121-30. doi: 10.1128/JVI.01704-06.

本文引用的文献

1
High resolution mapping of the B cell epitopes of staphylokinase in humans using negative selection of a phage-displayed antigen library.
J Immunol. 1998 Sep 15;161(6):3161-8.
2
The role of structure in antibody cross-reactivity between peptides and folded proteins.结构在肽与折叠蛋白之间抗体交叉反应中的作用。
J Mol Biol. 1998 Aug 7;281(1):183-201. doi: 10.1006/jmbi.1998.1907.
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Stochastic modeling and optimization of phage display.噬菌体展示的随机建模与优化
J Mol Biol. 1998 Apr 10;277(4):893-916. doi: 10.1006/jmbi.1997.1555.
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Peptide mimics of the CTLA4-binding domain stimulate T-cell proliferation.CTLA4结合域的肽模拟物刺激T细胞增殖。
Nat Biotechnol. 1998 Mar;16(3):267-70. doi: 10.1038/nbt0398-267.
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Identification of a 13 amino acid peptide mimetic of erythropoietin and description of amino acids critical for the mimetic activity of EMP1.促红细胞生成素的一种13氨基酸肽模拟物的鉴定以及对EMP1模拟活性至关重要的氨基酸的描述。
Biochemistry. 1998 Mar 17;37(11):3699-710. doi: 10.1021/bi971956y.
6
Photoaffinity labeling of the human receptor for urokinase-type plasminogen activator using a decapeptide antagonist. Evidence for a composite ligand-binding site and a short interdomain separation.使用十肽拮抗剂对人尿激酶型纤溶酶原激活剂受体进行光亲和标记。复合配体结合位点和短结构域间间隔的证据。
Biochemistry. 1998 Mar 17;37(11):3612-22. doi: 10.1021/bi972787k.
7
Small binding proteins selected from a combinatorial repertoire of knottins displayed on phage.从噬菌体展示的结蛋白组合文库中筛选出的小结合蛋白。
J Mol Biol. 1998 Mar 27;277(2):317-32. doi: 10.1006/jmbi.1997.1621.
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Phage-displayed mimotopes elicit monoclonal antibodies specific for a malaria vaccine candidate.
Biol Chem. 1998 Jan;379(1):65-70. doi: 10.1515/bchm.1998.379.1.65.
9
Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model.在小鼠模型中通过靶向药物递送作用于肿瘤血管系统进行癌症治疗。
Science. 1998 Jan 16;279(5349):377-80. doi: 10.1126/science.279.5349.377.
10
The three-dimensional structures of a polysaccharide binding antibody to Cryptococcus neoformans and its complex with a peptide from a phage display library: implications for the identification of peptide mimotopes.一种针对新型隐球菌的多糖结合抗体及其与噬菌体展示文库中一种肽段的复合物的三维结构:对肽模拟表位鉴定的启示
J Mol Biol. 1997 Dec 12;274(4):622-34. doi: 10.1006/jmbi.1997.1407.

噬菌体展示肽库

Phage-displayed peptide libraries.

作者信息

Zwick M B, Shen J, Scott J K

机构信息

Biochemistry Program, Simon Fraser University, Burnaby, BC, Canada.

出版信息

Curr Opin Biotechnol. 1998 Aug;9(4):427-36. doi: 10.1016/s0958-1669(98)80017-7.

DOI:10.1016/s0958-1669(98)80017-7
PMID:9720267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3987777/
Abstract

Over the past year, significant advances have been achieved through the use of phage-displayed peptide libraries. A wide variety of bioactive molecules, including antibodies, receptors and enzymes, have selected high-affinity and/or highly-specific peptide ligands from a number of different types of peptide library. The demonstrated therapeutic potential of some of these peptides, as well as new insights into protein structure and function that peptide ligands have provided, highlight the progress made within this rapidly-expanding field.

摘要

在过去的一年里,通过使用噬菌体展示肽库取得了重大进展。包括抗体、受体和酶在内的各种各样的生物活性分子,已从多种不同类型的肽库中筛选出高亲和力和/或高特异性的肽配体。其中一些肽已展现出治疗潜力,肽配体所提供的关于蛋白质结构和功能的新见解,凸显了在这个快速发展的领域所取得的进展。