1401 ICEDDEEWYSAMCA QCNAREWSANYICR VCDQVQWMTRLACQ TCLEVNWLTRMACM MCEYSHWSGFAFCK TCKELQWLPRLRCL TCSPGLREWAHNCL RCEQSMWTQRLPCL ECEHWGGQSQVQCR ECEWTHNRYTHKCQ 10 Phage display (common panning) 2 PMID:18760481 Anti-WNV E protein monoclonal antibody E113 Envelope protein Not determined. Not determined. XC(X)10CX phage display library 1402 DCEIPKIPMDRKCW YCRTNQSGAFARCT LCAPCAVPGNEAWS LCEETPPNETTPCI HCRMYEKLHHTACL LCKTEARTRAAPCA QCETESDLLIPSCP HCGQNSHPMWRKCQ YCGELAHHKTFMCN RCSCRPPSEATTCK NCGSRTQYCKSRCT TCYSFPMQRAAACP GCKLAMTTTTLACH ACTSQLLSVPSCCC RCPYYTRHPSMRCN GCEMSCEIALVVCH ECPQSTSIGLFRCT FCLPTRESTGRACP ICTSHQHILKPMCE ACDPSTVMVPWPCS YCTPSDRFIPHPCS 21 Phage display (common panning) 2 PMID:18760481 Anti-WNV E protein monoclonal antibody E121 Envelope protein Not determined. Not determined. XC(X)10CX phage display library 1403 LCEIKRVYLRQECM ECTVGYRQQKQECM ACRRQLTDAQTTCL YCIMSEEKPMPRCT KCPKAQKDKELSCQ RCPERHGHHTPACP PCLGAHVRFGNECL QCEREGVKAICTCP VCAVFVVLRTAPCQ PCKLPEMQTEATCL IWSPSPVPPHDECK CCEAEVRHPQLQCV KCSHLAPEATLECN KCSRPARARPTNCE LCPESRVHSRTVCP KCAHRTQPPACMCE SCEMSQQVLIRSCS ACVHSTHRLQENCP PCMGESAETTSKCP TCAGTGEICTSDCE VCTNTLAWSAVLSC GCGTRKRTESQTCK PCGHSMNQHEGSCT FCNPRLTTRPPHCR PCDAPVPEYPTDCG SCNQIRQIRESPCL RCERPNTTGTFSCD ICERVEYQVCSYCR RCGEQWPTKEAPCK NCNLLRPYSFSACS KCPPLSHPATSTCT TCPSPPPMMSTTCL TCAESYPPKMAGCL TCKQNRSWRAKECP LCELGAESREPECK KCAHQNSTTQNMCH ACQSTATQKEPTCR HCASTPQPYEPPCE ACPARLSRPASICP RCESNGPQCTEACR FCEPLWRQDRTLCH RCEPHELESPIGCR ACWQRESQTKDNCC SCLTLRTPATESCA RCRTERDSMCERCR ICNLDQQTSVRDCP TCTQTSQQGSMMCR QCPMLHKVTPLECV QCPNWYSIKTGACV SCAPTLNRHAHECL QCCSEQAGPRIACT TCQMRPRSLFSPCG TCYSMHTMSYGLCA TCYVNILTQPEICA NCRKMEPPAETECA FCETTSYTPPGECL LCAYPAPSKEMSCP TCTSAPHNSREMCK LCIPNPEMRQAPCW QCEHMEFKGHNKCH SCLQEELAAEKYCL PCQRMRAENTQRCA ACEESRTRPASTCR HCNQLSSFAAKKCN HCSCLLSAPKPACE QCQSIPFRTPEACP RCTTRRPRLQDFCE PCPHSMEAHADLCH YCAMLSPTPELRCT RCKEAHPTEPSLVG HCRTSGGETATACL QCAEKVPFCAKHCA LCPETPLCTKSICP ECYHWYPPEGKQCP QCRWIQSGTKKNCY ACIQEIRPPSSQCK SCPGLGQRKGAHCE VCENKNQAQKPWCA ECTYRTRAMPTTCS ECSPAASMKSTSCG ICHYEVPRSLTTCR VCPSTYLKNENHCF ECDQRPTVAPGFCK LCTDEKSALVSTCP SCHEQQRRPVAWCQ KCMMLELISTKACG ECPGSQPQCQSRCT DCAMMNLRTPPHCQ VCQNLRNRLPMECF ECIRPKQPNWTMCW QCGHCDDMETSECL PCTASQTPHGSECI HCHPSTAPEIRSCS ACTVPVTMWNNLCR WCLPLGVTPRDLCQ ACRTKEMPGKNPCS NCPNPKLPHWAPCP NCEWATHAATVTCA ECNSNEPGTPSACV ECPLRPPESSSTCA DCLTPGPCETNYCP TCKTETDLSMYQCR GCKTPQESNNTACH RCEPHELESPIGCL LCHKHTHECRTHCR TCLEPSSSSLAECK VCEEHEPRDRTQCA LCMQSELITDTPCP NCVQPELVTPPTCL 109 Phage display (subtractive panning) 3 PMID:19038455 Anti-WNV polyclonal antibody West Nile virus, WNV Not determined. Not determined. XC(X)10CX phage display library The phage library was first depleted of phage particles reactive to normal human serum (pooled from five non-infected individuals) by adsorbing the phage library to normal human antibodies bound to Protein G-sepharose. 1404 CRTCAHPGEHA CGPFYLSAPQC CGPFFLSPTSC CGPFFLAASVC 4 Phage display (subtractive panning) PMID:7514533 Anti-HBsAg polyclonal antibody Hepatitis B surface antigen Not determined. Not determined. pVIII-9aa.Cys phage display library (CX9C) Twelve serum-coated beads were pre-incubated with an excess of M13K07-UV killed phage. 1405 TENFNMWKNDMVEQMH RSNFEAWKWDEAQQGGS RENQTRWYRDMGGDMSS ASYLQWVRDTWVSL ASYWKDWLHDTAGGGVW ADYWRGWKERYNRSL EANYNAWREWVRSDWVS REYVYLWWIDHKTSL 8 Phage display (common panning) 3 PMID:8798975 Anti-gp120 monoclonal antibody GV4D3 Surface protein gp120, SU Not determined. Not determined. X20 phage display library 1406 QMHEDIISLWDQSLKPC ASIVSLWDSL DSRSDIWSIWSLGRERS PKRRSASELWGPSL SAHSPIEGLWAGESL GWREGVVGLWDRHSL YPRETAIQLWSL RGSVSIRDLWRSL 8 Phage display (common panning) 3 PMID:8798975 Anti-gp120 monoclonal antibody GV1A8 Surface protein gp120, SU Not determined. Not determined. X20 phage display library 1407 IHYCAPAGFAILKCNNK SGQREHVGFAILSL TRGGAAAGFAVHGSLSL VVARDHTGFAVLGTSL TDLMHCSGFALSPGCPQ ASMNGKVGWAIHAREAV SDDSSHTGWAVLDLGLR ASKTGVGWAVL QDMVRRPGWALLHPQLG 9 Phage display (common panning) 3 PMID:8798975 Anti-gp120 monoclonal antibody GV4H3 Surface protein gp120, SU Not determined. Not determined. X20 phage display library 1408 KVVKIEPLGVAPTKAKR GGLQRAALGVAPRT LSSKEGALGVAPPLTRT GGGLIKVLGVAPEGDSG PGALGVAPRVMER AGRAEWPLGIAPG ARGVAPDPTEH RVRKVEPLGVRVTA KVGKRSPLGIGPHAGG 9 Phage display (common panning) 3 PMID:8798975 Anti-gp120 monoclonal antibody GV1G2 Surface protein gp120, SU Not determined. Not determined. X20 phage display library 1409 XNNKFTSPPMSL DHGASSFHVSSX SDLNTDPSHPST LPLVVTPTSANG LKPISSHPSTVA HDQSPYXTVYGN SYQRAHHPPVLR STSQPTVSTLRP QHKTQPLNVISF TTTLSLVPLRPN GYSLYPIITSQK HTPHPMNLVAEA QTPPMQSPSATE SYSSPPSKAVRE HAPSYPLETKLM FYDSQPQVLSTT MPLMPTARSSMS GPRPPAALPHPL QSSYQTPXTPQP YXTALLHTPAED HTPHPDASIQGV YSNASARELGAT 22 Phage display (common panning) 3 PMID:9878399 Paclitaxel (Taxol) Apoptosis regulator Bcl-2 Not determined. Not determined. Ph.D.-12 phage display library (X12) Thirty micrograms of C7-biotinylated paclitaxel solubilized in HPLC-grade dimethylsulfoxide and diluted into Trisbuffered saline plus Tween 20, was attached to a streptavidin-coated petri dish. Each selection was performed on the streptavidin-coated petri dish. A subset of the peptides was identified that exhibits significant similarity to a non-conserved region of the anti-apoptotic human protein Bcl-2: ELISA assays conffirmed binding of paclitaxel to Bcl-2, and circular dichroism spectroscopy demonstrated that a substantial conformational change accompanies this binding. In vivo, treatment with paclitaxel has been shown to lead to Bcl-2 inactivation with concomitant phosphorylation of residues in a disordered, regulatory loop region of the protein. Similarity between paclitaxel-selected peptides and this loop region implicate these residues in drug binding, and suggest that the apoptotic action of paclitaxel may involve the binding of paclitaxel to Bcl-2. 1410 CKSSGKLISLC[14.98 ± 2.51, 11.73 ± 1.78] CGTKLVCFAAC[12.72 ± 2.11, 14.09 ± 2.18] CCNGRLYCGPC[13.87 ± 2.07, 1.02 ± 0.00] CCAGGLTCSVC[13.73 ± 2.64, 12.50 ± 1.30] CSGRLYCHESWC[18.74 ± 1.30, 10.23 ± 1.30] 5 Phage display (subtractive panning) PMID:10229859 Anti-HIV-1 polyclonal antibody Human immunodeficiency virus type 1, HIV-1 Not determined. Not determined. pVIII-9aa.Cys phage display library (CX9C) ELISA Comparison of ELISA reactivities of phagotopes with sera of LTNP vs AIDS subjects was performed by ELISA. The difference between OD405 nm and OD620 nm was determined by an ELISA reader. Data are expressed as fold increase of the average values of the phagotopes over values of the wild-type phages and as mean ± SEM of fold increase for each phagotope. Data shown are reproduced from Fig. 1B in the reference. Data in the first column are values of phagotopes with sera of LTNP. Data in the second column are values of phagotopes with sera of LTNP. Values were considered positive when at least 4-fold higher than the background signal of wild-type phage. In the immunoaffinity selection, serum IgG was linked to magnetic microbeads previously coated with an anti-human (Fc-specific) polyclonal Ab of beads suspension. Given the fact that sera from long-term nonprogressor (LTNP) subjects show higher titers of neutralizing Abs than sera from AIDS patients, initial screening was performed with LTNP sera. 1411 EATFVYPAP[12.23 ± 1.74, 12.02 ± 2.08] TKTLIYGGA[13.73 ± 2.41, 11.48 ± 1.94] KRIVIGPQT[17.49 ± 1.83, 9.55 ± 1.93] FASLHYDKP[13.92 ± 2.17, 10.52 ± 1.40] RPTLRFQGA[11.56 ± 1.88, 13.32 ± 1.16] 5 Phage display (subtractive panning) PMID:10229859 Anti-HIV-1 polyclonal antibody Human immunodeficiency virus type 1, HIV-1 Not determined. Not determined. pVIII-9aa phage display library (X9) ELISA Comparison of ELISA reactivities of phagotopes with sera of LTNP vs AIDS subjects was performed by ELISA. The difference between OD405 nm and OD620 nm was determined by an ELISA reader. Data are expressed as fold increase of the average values of the phagotopes over values of the wild-type phages and as mean ± SEM of fold increase for each phagotope. Data shown are reproduced from Fig. 1B in the reference. Data in the first column are values of phagotopes with sera of LTNP. Data in the second column are values of phagotopes with sera of LTNP. Values were considered positive when at least 4-fold higher than the background signal of wild-type phage. In the immunoaffinity selection, serum IgG was linked to magnetic microbeads previously coated with an anti-human (Fc-specific) polyclonal Ab of beads suspension. Given the fact that sera from long-term nonprogressor (LTNP) subjects show higher titers of neutralizing Abs than sera from AIDS patients, initial screening was performed with LTNP sera. 1412 NTAHSDMHSP(2) KAEERFHEVR(1) WNIFQSLSSP(1) RVAATAAREE(1) TPEPLEEAAS(1) DHVFKRPQPS(1) ETCVEKNEAD(1) WRRDGC(1) YMDPHTQREA(1) EPVRDNCAPS(1) VERDIATRPW(1) ERPEIEDVCQ(1) QKTLNTSNAN(1) VKTLNTSNAN(1) RDTTMWEVNA(1) WGHCSQGMIE(1) PPFDVFHNPM(1) DTHAGMHSPT(1) RMPHHDPQLM(1) TQNLMQMQHA(1) SPFMLMHGEH(1) TCQAGRESMHNP(1) WETMHNPGTP(1) DALNMHEGRP(1) SKLETTMHSP(1) LGGMDSMHSP(1) MAQMHEPVRS(1) LPQHNMMHDP(1) PSNYSAMHAP(1) RCETHFNMHEPY(1) 30 Phage display (subtractive panning) 2 PMID:19390580 Anti-HER-2 extracellular domain polyclonal antibody Extracellular domain of HER-2 Not determined. Not determined. XC(X)10CX phage display library The library was initially depleted of phages recognized by naive mouse serum by 3 sequential pannings of the library with immobilized serum of non-immunized mice. The resultant \"depleted\" library was used for mimotope identification. Similarly, the sera obtained from immunized mice were initially depleted of anti-phage activity by overnight incubation at 4 ℃ with wild type phage immobilized on plastic plates. The sera were also depleted of IgM by similar incubation with immobilized anti-IgM antibody. 1413 NWSIAGD(1) SRGDTEP(1) TSDSWQR(1) PKTEVPQ(1) DDFSPPR(1) EWYTPQG(1) SRCDLDEKGC(1) PRCKHNQKKC(1) AGACKRMREF(1) ATPKRTHDHD(1) TSNNRVEARA(1) RTTPSGGGFK(1) DGWYVAQ(1) GGRWGES(1) WYTTPGS(1) SGWYTPV(1) AKDEQPM(1) GWYVSSP(1) PSEGQSE(1) GTAGGEITEH(1) FYSSMFWAVGEQ(1) LQEFPGDQLV(1) LSTRLWIPAW(1) KTTTWPSTPT(1) MWASVNKMA(1) PPPLLAGDPK(1) AVNQCTTVLA(1) GTAGGEITEHE(1) 28 Phage display (subtractive panning) 2 PMID:19390580 Anti-HER-2 polyclonal antibody Receptor tyrosine-protein kinase erbB-2 Not determined. Not determined. XC(X)10CX phage display library The library was initially depleted of phages recognized by naive mouse serum by 3 sequential pannings of the library with immobilized serum of non-immunized mice. The resultant \"depleted\" library was used for mimotope identification. Similarly, the sera obtained from immunized mice were initially depleted of anti-phage activity by overnight incubation at 4 ℃ with wild type phage immobilized on plastic plates. The sera were also depleted of IgM by similar incubation with immobilized anti-IgM antibody. 1414 TYSGRAACGV(1) SASMPFPANE(1) SKPKYEKPSQ(1) EVTTEHVEAN(1) RSHERHPPSP(1) DDELHSGTSY(1) SPPAFSHPMQ(1) VNTQGPNSIA(1) 8 Phage display (subtractive panning) 2 PMID:19390580 Anti-HER-2 polyclonal antibody Receptor tyrosine-protein kinase erbB-2 Not determined. Not determined. XC(X)10CX phage display library The library was initially depleted of phages recognized by naive mouse serum by 3 sequential pannings of the library with immobilized serum of non-immunized mice. The resultant \"depleted\" library was used for mimotope identification. Similarly, the sera obtained from immunized mice were initially depleted of anti-phage activity by overnight incubation at 4 ℃ with wild type phage immobilized on plastic plates. The sera were also depleted of IgM by similar incubation with immobilized anti-IgM antibody. 1415 ADTVSGAMV(7) VARVGSPPD(7) VAVVGTFPD(5) VSTPGSPDD(5) ASYQDLGSS(4) AEMVKSSID(4) DFVTRSPQD(4) EWDPAPAME(4) ARGGEGTED(3) DNGSLANGE(3) DRRDDAVSE(3) ENARSVNDD(3) EYSAPSADA(3) GDYQSLVED(3) GMNNASFPD(3) GSPSEYSSQ(3) VPQTSLAME(3) EGGGGLIND(2) ESGGSGSTE(2) GETLDPSLE(2) GGTESMTAS(2) VFLGDPSVE(2) VSATLEPVD(2) ADGSPDLPA(1) AEGGLEHLD(1) AEYAFGGTD(1) AFGAQEDNT(1) AFNATASMS(1) AGSNINLVD(1) AHMSEVEGG(1) AIRDIAGDS(1) AITASDSMS(1) ANRVSEMTE(1) ANSISFDDD(1) APDSSAWSD(1) APNLSISDS(1) APTVEADNN(1) AQDLAVITG(1) AQYETSYPE(1) ASSHFDGSD(1) AYESGTGSS(1) DEHMEGNAG(1) DGFADLASD(1) DGRPSDIPT(1) DGVADAASN(1) DSGGSGIAS(1) DVSGAFMAD(1) EAGPIPGDG(1) EDISLSMGE(1) EDYPDISVG(1) EETMNGMPM(2) EFNDGSGVD(1) EHELDPVMA(1) EIGGMGAGG(1) EMERSSSMA(1) ENPVLASDS(1) ESSTQDFPD(1) EWVDPRGED(1) EYSSSELPP(1) GATHEVGGD(1) GDLVQDVTA(1) GESSGGADD(1) GGDFAAANG(1) GLRGEVEEG(1) GMQAGDQDD(1) GPVEGDADG(1) GSDSDLTFD(1) GSGGAENVS(1) GSLDDITDN(1) GSRDGVISE(1) VEGQGSVSD(1) VGDAGHSME(1) VGEGYREES(1) VGRDSTLND(1) VGTDSNDAG(1) VLDSVSSPD(1) VLPVGAGTD(1) VNENQLVMD(1) VNVTDAGID(1) VPAAYIGND(1) VTANPDSSA(1) VTMFESNAD(1) VTNDPSLDD(1) VVNQGDPPD(1) VVRDPGVSG(1) VYQNSESTL(1) 86 Phage display (subtractive panning) 3 PMID:19186939 α, β-tubulins from bovine brain Microtubule-associated proteins (MAPs) Not determined. Not determined. f8-9mer phage display library (X9) The landscape phage library was added to the untreated dish at 4 °C to remove the phages that specifically bound to the Petri dish. The tubulins received have been modified so that random surface lysines contain a covalently linked, long-chain biotin derivative. This long-chain biotin derivative enables the immobilization of the tubulins on the streptavidin-coated Petri dish. By using RELIC, the affinity-selected peptides were shown to have similarity with the sequences of two MAP families (MAP1 and MAP2/tau), thereby identifying putative microtubule-binding domains on these MAPs. The tubulin-binding affinity was also confirmed by using transmission electron microscopy (TEM) to characterize the interaction between affinity-selected tubulin-binding phage and tubulins. 1416 YTRSEGVLLQLT(1)[++] FGCRVESVSTHC(1)[+++] CRNQAVRVFCHN(1)[+++] EKPSESRIAQLG(1)[++] KGFRMEAVWRRF(1)[+] YVWKIVTEGVNV(1)[+] RKRCFHALDCLG(1)[+] R-x-[EQ] 7 Phage display (subtractive panning) 2 PMID:18707547 Anti-CD6 monoclonal antibody ior t1 T-cell differentiation antigen CD6 Not determined. Not determined. pVIII-9aa phage display library (X9) ELISA The affinities of the selected clones to anti-CD6 monoclonal antibody ior t1 were analyzed by ELISA assay. The absorbance was measured at 492 nm. Symbols represent the optical density values obtained for each antibody as follows: (+) from 0.3 to 0.5; (++) from 0.6 to 1.0; (+++) from 1.1–2.0. Polystyrene beads were preincubated with approximately M13K07 UV-killed phage particles. 1417 KGIPNTKAP[0.589] DMFQIGKYG[0.405] GIREVWPAG[0.917] SSMGAYWGG[0.241] KGTTGVRNT[0.441] 5 Phage display (common panning) 3 PMID:17964653 Anti-Der p 1 monoclonal antibody Peptidase 1 Not determined. Not determined. J404 phage display library (X9) ELISA Der p 1-specific was coated on ELISA plates and incubated with selected single phage clone amplificates. The detection was carried out with anti-phage antibody at 405-490 nm. For negative control wild-type phage (wt) lacking the specific insert was used at the same concentration as the selected phage clones. Absorbances at 405-490 nm were reproduced from the graph and shown. The absorbance for negative control was 0.064. To identify single phage clones, 120 random phage clones were screened by a colony screening ELISA. On this ELISA, five phage clones showed a significantly higher binding signal to the specific antibody in comparison to background reactivity with wild-type phage. No binding of these clones was detected to the control antibody. 1418 FVVEYTKKW[0.229] SWWNLPQIG[0.358] KGITTKWMA[0.419] AGISYTKTW[0.702] 4 Phage display (common panning) 3 PMID:17964653 Anti-Der p 2 monoclonal antibody Mite group 2 allergen Der p 2 Not determined. Not determined. J404 phage display library (X9) ELISA Der p 2-specific was coated on ELISA plates and incubated with selected single phage clone amplificates. The detection was carried out with anti-phage antibody at 405-490 nm. For negative control wild-type phage (wt) lacking the specific insert was used at the same concentration as the selected phage clones. Absorbances at 405-490 nm were reproduced from the graph and shown. The absorbance for negative control was 0.067. To identify single phage clones, 120 random phage clones were screened by a colony screening ELISA. On this ELISA, four phage clones showed a significantly higher binding signal to the specific antibody in comparison to background reactivity with wild-type phage. No binding of these clones was detected to the control antibody. 1419 PSYNASLDCPYSVGD FSYRSSYVPSSRRSA RCEVWPCRSSPHLNP CGVGHCLPFFCFPSF DYFVTPCCWVSRLTL CRRVVCFCDGYCLAD FYSCMFPYAASASFV TLLFVSVPACFGPHA PLSEIFYFGCCYDSV SGVTCCDSSRALCGS GLSVMCNPVLDPVCK PMGYFSFPWNTDVVA FIRHSITLKCAARGG YLFLNVIGSDSFVFD LVDNCILTVFPPHNA LDMFSFPSVCFGTCI RGVSLCHASASSTQY SFYRSDGVLCPIVPW LGNLCHFNAMGLADG VCGLVHVKSLAPPAW VYDASVFGVWTPLHG WATVVADALHLGGFS CCFSGSHLVPYAKGT FFSLTGVPGNVFCLS CVFDVRSAADSFLAV CGNCCVYLDADNDVP SIALGCRGFWYFDLP TVLFALMRSGADGIW FCISHILNYPFDGDA AFLSFSRPLWPSFFC VCLGVGVGFVADCPD LVGALGVTVRHALGT LFHLYCDFDAPLAAW LMICAGRWRSGSFVD CVFFISLNGAACCVG 35 Phage display (common panning) 1 PMID:18930404 Synthetic ligand for FK506-binding protein, SLF Not determined. Not determined. Not determined. X15 T7 phage display library The screening procedure involved a cuvette type 27-MHz quartz-crystal microbalance (QCM) apparatus with introduction of self-assembled monolayer (SAM) for a specific small-molecule immobilization on the gold electrode surface of a sensor chip. For SLF-bio immobilization, the gold sensor surface was initially coated by treatment with 100μl of neutravidin solution (100lg/mlaq) for 30 min at room temperature. After washing the gold electrode surface, SLF-bio was applied and left for 16 h under a humid and shaded atmosphere at room temperature. The gold surface was thoroughly washed prior to conducting the screening experiments. 1420 CDRRACRVAFSSRTG LVFSLFVILLLVLGV FGFFSSNPLVHVHWD FIPAYCCVVCAYLSV GYFNCLVVHRHALRC LSSLCGLPFGRPQCV SFARLLFRLCLTTTP FFFGGLRLLVLLRES FFYRLVFCHYPRLVF DCSRFSWLSSVFAVA HLYGFSLIMFCMVTI SLVLFTSNVYPMFVF WDSSCFVPFLCSGSS CSDIVVASPSPFPTC CVLSLCLFMVLFFSV FFLPVGFRAFLLGRR FVDSCLLCTFTTLRT LFVLSSSDAHECSAY RCVLSYGPNVFQPVD SFCISCLCVCGGDGR SFDAALCLVSSLFGA TGSHCGVYKVGLGVV VTYFTWSFDPRGCCW VVVIVFLCLVWLVGG YVLWWRLLFFILIIS YYAIFFHRVLRMYSV SFDFGSFDFVSPLAP CIDVNCFVWTFGMPF FGYELSFLSSWSVFG 29 Phage display (common panning) 1 PMID:18930404 Irinotecan, Iri Not determined. Not determined. Not determined. X15 T7 phage display library The screening procedure involved a cuvette type 27-MHz quartz-crystal microbalance (QCM) apparatus with introduction of self-assembled monolayer (SAM) for a specific small-molecule immobilization on the gold electrode surface of a sensor chip. For Iri-bio immobilization, the gold sensor surface was initially coated by treatment with 100μl of neutravidin solution (100lg/mlaq) for 30 min at room temperature. After washing the gold electrode surface, Iri-bio was applied and left for 16 h under a humid and shaded atmosphere at room temperature. The gold surface was thoroughly washed prior to conducting the screening experiments. 1421 PLDMIGTYQHIM(60) 1 Phage display (common panning) 3 PMID:18383103 Anti-transferrin monoclonal antibody hTf345 Serotransferrin, Transferrin Not determined. Not determined. X12 phage display library 1422 EPVESPWSRARL(2) VVGTDPFSRARL(4) AGPRDPYGV(1) QGMKSPYDSARL(1) LEYDPHHVARV(1) TLQTTPHDVARL(1) KKFKMGPPV(1) ETPTPWGRARV(4) TLQTTPHDVARR(4) SQGKTPFDIGRR(1) DPHWVGRV(1) GDPHYVARV(1) 12 Phage display (common panning) 3 PMID:17397983 Anti-b558 monoclonal antibody 7A2 Cytochrome b-245 heavy chain Not determined. Not determined. J404 phage display library (X9) 1423 SCTDDPWCTARV(9) HERGDPHYVARV(1) RIVQDPVDVARR(1) DRERDPWLVARR(1) RWNHTSERV(1) 5 Phage display (common panning) 3 PMID:17397983 Anti-b558 monoclonal antibody 8G11 Cytochrome b-245 heavy chain Not determined. Not determined. J404 phage display library (X9) 1424 DHQRFFV(5) AHQASFV(1) 2 Phage display (common panning) 3 PMID:11292756 Anti-E. coli K1 monoclonal antibody HmenB1 Escherichia coli K1 bacteria Not determined. Not determined. Ph.D.-7 phage display library (X7) The new mimotopes may be useful in producing a vaccine(s) capable of eliciting anti-NMGB antibodies not reactive with neuronal tissue. 1425 SHVPNAF(23) SHAPNAF(6) SHVPDAF(4) SHVHNAF(2) SHAPSAF(1) SHVPHAF(1) 6 Phage display (common panning) 3 PMID:11292756 Anti-E. coli K1 monoclonal antibody HmenB3 Escherichia coli K1 bacteria Not determined. Not determined. Ph.D.-7 phage display library (X7) The new mimotopes may be useful in producing a vaccine(s) capable of eliciting anti-NMGB antibodies not reactive with neuronal tissue.