HWGMWSY, an unanticipated polystyrene binding peptide from random phage display libraries

被引:27
|
作者
Vodnik, Miha [1 ]
Strukelj, Borut [1 ,2 ]
Lunder, Mojca [1 ]
机构
[1] Fac Pharm, Dept Pharmaceut Biol, Ljubljana, Slovenia
[2] Jozef Stefan Inst, Dept Biotechnol, Ljubljana, Slovenia
关键词
Target-unrelated peptides; Phage display; Plastic binding; HWGMWSY; SELECTION; VIRUS;
D O I
10.1016/j.ab.2012.02.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phage display is a powerful technique for the discovery of peptide ligands that bind to various targets; however, ambiguous results often appear. Peptide HWGMWSY has been isolated repeatedly in our laboratory and by other research groups dealing with different protein and nonprotein targets, which led to a hypothesis that it may be a target-unrelated peptide interacting with polystyrene plastic surfaces. We compared binding properties and amplification rate of phage clone displaying the peptide HWGMWSY, a previously confirmed plastic binding clone WHWRLPS, and a control phage clone ASVQERK. An enzyme-linked immunosorbent assay and a phage elution assay confirmed that phage clone HWGMWSY binds to polystyrene. Surface plasmon resonance measurements on the other hand excluded the possibility of binding to bovine serum albumin, a common blocking agent in phage display experiments. Amplification rates of the above-noted phage clones were not statistically different. We therefore conclude that phage clone HWGMWSY was isolated in different selection procedures as a result of its affinity to polystyrene. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:83 / 86
页数:4
相关论文
共 50 条
  • [21] Identification of peptides binding to presenilin 1 by screening of random peptide display libraries
    Schwarzman, A
    Tsiper, M
    Vitek, M
    St George-Hyslop, P
    Goldgaber, D
    PROGRESS IN ALZHEIMER'S AND PARKINSON'S DISEASES, 1998, 49 : 141 - 147
  • [22] A DNA-binding peptide from a phage display library
    Wölcke, J
    Weinhold, E
    NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 2001, 20 (4-7): : 1239 - 1241
  • [23] A PEPTIDE ISOLATED FROM PHAGE DISPLAY LIBRARIES IS A STRUCTURAL AND FUNCTIONAL MIMIC OF AN RGD-BINDING SITE ON INTEGRINS
    PASQUALINI, R
    KOIVUNEN, E
    RUOSLAHTI, E
    JOURNAL OF CELL BIOLOGY, 1995, 130 (05): : 1189 - 1196
  • [24] Phage display for the identification of a hepatoma binding peptide
    Prenzel, T.
    Altmann, A.
    Mier, W.
    Kraemer, S.
    Eisenhut, M.
    Haberkorn, U.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2007, 34 : S395 - S395
  • [25] Isolation of a tau binding peptide by phage display
    Huang, Xianlong
    Zheng, Zhiwen
    Wu, Yixin
    Su, Zhengding
    Huang, Yongqi
    BIOPHYSICAL JOURNAL, 2022, 121 (03) : 352A - 352A
  • [26] An improved selection procedure for the screening of phage display peptide libraries
    D'Mello, F
    Howard, CR
    JOURNAL OF IMMUNOLOGICAL METHODS, 2001, 247 (1-2) : 191 - 203
  • [27] Organ targeting in vivo using phage display peptide libraries
    Pasqualini, R
    Ruoslahti, E
    NATURE, 1996, 380 (6572) : 364 - 366
  • [28] Phage Display of Combinatorial Peptide Libraries: Application to Antiviral Research
    Castel, Guillaume
    Chteoui, Mohamed
    Heyd, Bernadette
    Tordo, Noel
    MOLECULES, 2011, 16 (05) : 3499 - 3518
  • [29] Probing antinuclear antibody specificities by peptide phage display libraries
    Hansen, MH
    Dybwad, A
    Forre, O
    Sioud, M
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2000, 18 (04) : 465 - 472
  • [30] A minimalistic cyclic ice-binding peptide from phage display
    Stevens, Corey A.
    Bachtiger, Fabienne
    Kong, Xu-Dong
    Abriata, Luciano A.
    Sosso, Gabriele C.
    Gibson, Matthew, I
    Klok, Harm-Anton
    NATURE COMMUNICATIONS, 2021, 12 (01)