<result><BiopanningDataSet><Item><BiopanningDataSetID>2876</BiopanningDataSetID>
<Peptides>YHTTDKLFYMMR[1.78 ± 0.08]
YSAYEFEYILSS[1.71 ± 0.05]
KTMSAEEFDNWL[1.95 ± 0.11]
LTSHTYRSQADT[0.68 ± 0.12]</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>4</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:26033236</Reference>
<Target_Name>Tocilizumab</Target_Name>
<Template_Name>Interleukin-6 receptor</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method>ELISA</Affinity_Measurement_Method>
<Affinity_Measurement_Description>Binding capabilities of the selected phages toward Tocilizumab was estimated by ELISA. The absorbance at 405 nm was measured and data shown were reproduced from the Fig. 1C in the reference. The experiments were performed in triplicate and presented as mean ± standard deviation.</Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>The mimotopes were conjugated to immunogenic carrier proteins and used to intraperitoneally immunize BALB/c mice. Sera from the mimotopes immunized mice not only showed specific binding to recombinant IL-6R, but can also IL-6R expressed in Hela, U-937, Jurkat cell lines and in fibroblast-like synoviocytes from patients with RA (FLS-RA).</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2877</BiopanningDataSetID>
<Peptides>NKELQTV(7)[1.56 ± 0.2, 0.68 ± 0.18]
VKELDTR(3)[1.78 ± 0.32, 1.22 ± 0.16]
AKELSTW(2)[2.25 ± 0.23, 0.79 ± 0.32]</Peptides>
<Motif>K-E-L-x-T</Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:26048649</Reference>
<Target_Name>Imidacloprid hapten IMI</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-7 phage display library (X7)</Library_Name>
<Affinity_Measurement_Method>ELISA</Affinity_Measurement_Method>
<Affinity_Measurement_Description>The binding activities of positive phage clones to IMI-BSA were measured by competitive phage ELISA respectively using 0 and 1000 ng/mL of imidacloprid. The absorbance at 450 nm was measured and data shown were reproduced from the Figure 2 in the reference.</Affinity_Measurement_Description>
<Brief_Description>The conjugate IMI-BSA was used as binding-templates to select peptides specific for imidacloprid. Bound phages in the wells were eluted. The eluted phage solutions were transferred onto wells coated with 3% BSA alone to eliminate the non-specific binding phages.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2878</BiopanningDataSetID>
<Peptides>PHSNRKKKDTQR[23.95 ± 0.38]
HYKYYPTASVMK[104.1 ± 0.76]
FTKVKPKSHNMT[23.95 ± 3.02]
WPLSTVASVRVP[39.52 ± 2.67]
VPRSMAATHSTF[14.83 ± 2.64]
PHSNRKKNQYLE[23.19 ± 5.3]
QTWDLPRTTHKT[11.79 ± 2.28]</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (competitive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:26052070</Reference>
<Target_Name>Site-specifically biotinylated Complement C3 beta chain (C3b)</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method>Surface plasmon resonance (SPR)</Affinity_Measurement_Method>
<Affinity_Measurement_Description>Direct binding of peptides was measured using SPR by injecting 1 mM of each peptide over site-specifically immobilized C3b. Data shown were reproduced from the Fig. 4B in the reference. A control peptide (YHPNGMNPYTKA) exhibits minimal response at this concentration, which had the Resonance Units (RU) value of 3.81 ± 0.76.</Affinity_Measurement_Description>
<Brief_Description>Following washes of increasing stringency, bound phage were eluted using 100 μM MSCIN-A to specifically select for SCIN-competitive, C3b-binding sequences.</Brief_Description>
<BiopanningDataSet_Comments>Seven unique sequences exhibited direct C3b binding. A subset of these specifically inhibited the AP inassays of complement function. The mechanism of AP inhibition by these peptides was probed through surface plasmon resonance approaches, which revealed that six of the seven peptides disrupted C3bBb formation by interfering with factor B/C3b binding.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2879</BiopanningDataSetID>
<Peptides>KVWMPNNRGPVP
AYTTSIPNRNQL
TILKAWPNITQL
AWPPPSMGPLAY
KISQPTTVASLQ
ILANDLTAPGPR
TPFPFAPLGRPP
KVWISPQSLGAT
VSRHQSWHPHDL
KCCTLPRPLEML
NQRVLPPSHSWL
LSLNFDRESETN
KVWPPMYLSHTF
AVPHRVGGLHSL
NADNQMTWRHVL
IDAPANQRLLQK
KIWQMDQDSVRN
HPHHETSVMRLQ
KVWXMAPTTAFS
SHPWNAQRELSV
KVWQLQPSNSVT
MKVSEPLHAHFS
KAWVLTEWQTTK
SIHRHHDDHFLT
LLXKTLNNRLYD
KVVQLSELSRLL
DPALRHTHHNLR
AHSHKLFLLSNR
HSPSNLGFQSPP
WMADTSPSLAST
SWNSKAWIVVPA
STMNDIHMELHR
KCCFTTASSTSI
GLKIWSLPPHHG
KIXIFYPFKSPLI
FPAMSFAXKKLA
HFKPMQPAHPIP
NSTLKVLPQGWM
KVWPPLTSIVPS
NLRTDSLTLVIR</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>40</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:26071378</Reference>
<Target_Name>Type IV secretion system protein virB10</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2880</BiopanningDataSetID>
<Peptides>DAQWAFM
PPLSAPN
GETPNPH
LSSPTSN
PLWDKRH
NSWPPSR
RLPHSVG
QWTNHAL
SGTPWHP
DPFHVHN
TTNSPPL
FSSSRNY
PATYTSA
TQPWTRA
NDFKLQF
YKLPSRH
ALGHSAK
QKAHHEQ
HEARSTM
VIPQPQQ
SYPTRPT
FGNPHGH
MRNDGAN
PVPYPQL
PKKLDSI
KATAQGA
HNPLLSF
KPASHNA
DSLQYPA
TLPLPNL
TNPVTES
MSKHQAY
PEAALSS
TFLDTRA
DPGASHP
MERPAHL
STHTSRL
WAAIFPL
PSKLQEH
GPKMFRI
LKITGED
NRYTPTA
LSYLHPT
HPQLPSI
NRGQLST
GFLGKNQ
KSAKTYH
APSPWKQ
PHTLSRT
FSNQTML
PAHRVPS
CSTPTPH
GMMPVAL</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>53</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:26071378</Reference>
<Target_Name>Type IV secretion system protein virB10</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2881</BiopanningDataSetID>
<Peptides>TQYYAYSTTQKS
TQAIRVHTISSQ
GLNQVLRIPSFI
SPKHNLDMVKMM
MIVDHLPIQVNT
EYDYACGVVGYE
SYPKASLALLAP</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:26058474</Reference>
<Target_Name>Magnesium fluoride (MgF2) particles</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2882</BiopanningDataSetID>
<Peptides>NQTHDWVPYAGR(8)
YWPDERPFAARK(4)
LHNPWRDTPPFA(4)
TALDFPTWTAKN(4)
VIDIPPFAYRNT(3)
YADTPPFASTHK(2)
STSDFLPYAARF(2)
LPGVRDTPPFAA(2)
VIGDMPPYAAMH(2)
QWDLPPYAGRYD(2)
GIDQLPWAARNK(2)
YGIPWLDMPIKR(2)
NQTDGQDRVPYA(1)
TSPDAYPYAARQ(1)
SDLPPFAAGRYN(1)
NPFDTVPYAGRQ(1)
RTLDWYDRVPYA(1)
IQDWPPYASSTK(1)
GERPPDYPPYAA(1)
NHNQDFRPFPDR(1)
KWQSDWPPFAAY(1)
SDVDRPPWPART(1)
SYVPDWPPFASK(1)
APNVTDVPPFAA(1)
IDTPPYAGRSSL(1)
TLLIQRSPYEQI(1)
SINPNPPLRPSY(1)</Peptides>
<Motif>D-x-[PVLP]-[YFW]-A-[AGS]-[RK]</Motif>
<Unique_Sequence_Number>27</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:25520269</Reference>
<Target_Name>Anti-coagulation factor VIII monoclonal antibody (mAb) 2-76</Target_Name>
<Template_Name>Coagulation factor VIII</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For selection of peptides that bind to the murine monoclonal anti-FVIII antibody (mAb) 2-76 immobilisation on streptavidin-coated beads was achieved via a biotin-conjugated rabbit anti-mouse IgG. For negative selections, an appropriate IgG isotype (murine IgG2a) was used. Three positive and two negative selections were performed.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2883</BiopanningDataSetID>
<Peptides>NPPKWPR(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:25520269</Reference>
<Target_Name>Anti-coagulation factor VIII monoclonal antibody (mAb) 2-76</Target_Name>
<Template_Name>Coagulation factor VIII</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-7 phage display library (X7)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For selection of peptides that bind to the murine monoclonal anti-FVIII antibody (mAb) 2-76 immobilisation on streptavidin-coated beads was achieved via a biotin-conjugated rabbit anti-mouse IgG. For negative selections, an appropriate IgG isotype (murine IgG2a) was used. Three positive and two negative selections were performed.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2884</BiopanningDataSetID>
<Peptides>NFTHPGV(2)
SSTVYGR(2)
SKLDGEK(1)
MHMYSPP(1)
YSTEYTY(1)
STHPLPP(1)
NGTRYLG(1)
WSRPPIM(1)
LTLPRSF(1)
FSAFPTS(1)
LTSPLHI(1)
RLPPQTP(1)
WSTSYTM(1)
DPKNQPA(1)
LSAIPTR(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>15</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:25520269</Reference>
<Target_Name>Anti-coagulation factor VIII polyclonal antibody IgG from haemophilia A patient 1</Target_Name>
<Template_Name>Coagulation factor VIII</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-7 phage display library (X7)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selections, IgGs from FVIII inhibitor-positive plasma was immobilized on streptavidin-coated beads via a biotin-conjugated goat anti-human IgG. For negative selections, IgGs from a plasma pool of healthy individuals negative for FVIII-specific antibodies were immobilised likewise.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2885</BiopanningDataSetID>
<Peptides>NYTHPGS(1)
WTHPGNR(1)
NFTHPGS(1)
WTHPGAQ(1)
SFTHPGQ(1)
YTHPGAA(1)</Peptides>
<Motif>T-H-P-G</Motif>
<Unique_Sequence_Number>6</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:25520269</Reference>
<Target_Name>Anti-coagulation factor VIII polyclonal antibody IgG from haemophilia A patient 1</Target_Name>
<Template_Name>Coagulation factor VIII</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selections, IgGs from FVIII inhibitor-positive plasma was immobilized on streptavidin-coated beads via a biotin-conjugated goat anti-human IgG. For negative selections, IgGs from a plasma pool of healthy individuals negative for FVIII-specific antibodies were immobilised likewise.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2886</BiopanningDataSetID>
<Peptides>SNDFIHTWSTNW(3)
DGNYTHTRSTNY(2)
TPPYLHHFSTRY(2)
QKSLHTFSTHYS(1)
NCWTHPGATQCN(1)
QGYNHVISTAYD(1)
LTPITQLAGPMP(1)
AIPYNHSVATYY(1)
MGAHYRPQPNPH(1)
LTYPDFLHNNFP(1)
MYIPNNTPSMMR(1)
LQVPWYATSTAK(1)
FITPPSLPAFTG(1)
ETQIHMVSTRYD(1)
SMNYYHTFATNY(1)
SPWLHTTSTHYL(1)
STASNFTHPGND(1)
SFTHRESTIYNA(1)
DMIHTHYSSTRY(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>19</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:25520269</Reference>
<Target_Name>Anti-coagulation factor VIII polyclonal antibody IgG from haemophilia A patient 1</Target_Name>
<Template_Name>Coagulation factor VIII</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selections, IgGs from FVIII inhibitor-positive plasma was immobilized on streptavidin-coated beads via a biotin-conjugated goat anti-human IgG. For negative selections, IgGs from a plasma pool of healthy individuals negative for FVIII-specific antibodies were immobilised likewise.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2887</BiopanningDataSetID>
<Peptides>AMRVEPHTYKNH(7)
AMLVDPQGAHSW(1)
NPVEWFMSTVNT(1)
GMKVEPWMPPPR(1)
YMPVEPQSTYTK(1)
AMPVESELYKLM(1)
AMPVAPDTQRYR(1)
SFNTRPLPFLSY(1)
AQRVDPDLVSIS(1)</Peptides>
<Motif>[AG]-M-x-V-[ED]-P</Motif>
<Unique_Sequence_Number>9</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:25520269</Reference>
<Target_Name>Anti-coagulation factor VIII polyclonal antibody IgG from haemophilia A patient 3</Target_Name>
<Template_Name>Coagulation factor VIII</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selections, IgGs from FVIII inhibitor-positive plasma was immobilized on streptavidin-coated beads via a biotin-conjugated goat anti-human IgG. For negative selections, IgGs from a plasma pool of healthy individuals negative for FVIII-specific antibodies were immobilised likewise.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2888</BiopanningDataSetID>
<Peptides>AMLVQPA(5)
AMPVEPD(2)
AMFVEPA(1)
AMLVFPE(1)
AMQVDPA(1)
AMPVQPH(1)
AMLVEPY(1)
LTLQPTF(1)</Peptides>
<Motif>[AL]-M-x-[VQ]-E-P</Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:25520269</Reference>
<Target_Name>Anti-coagulation factor VIII polyclonal antibody IgG from haemophilia A patient 3</Target_Name>
<Template_Name>Coagulation factor VIII</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-7 phage display library (X7)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selections, IgGs from FVIII inhibitor-positive plasma was immobilized on streptavidin-coated beads via a biotin-conjugated goat anti-human IgG. For negative selections, IgGs from a plasma pool of healthy individuals negative for FVIII-specific antibodies were immobilised likewise.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2889</BiopanningDataSetID>
<Peptides>SLQPTEHNKFWL(2)
MTTPTESHKFGH(1)
DLLRPSEKNKFF(1)
SYTPSELRVFQT(1)
TPAPSERMHFDS(1)
SPSELQKFQTRS(1)
KSTPSEIRHFDY(1)</Peptides>
<Motif>[TS]-P-[ST]-E-x(2)-[KH]-F</Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:25520269</Reference>
<Target_Name>Anti-coagulation factor VIII polyclonal antibody IgG from haemophilia A patient 5</Target_Name>
<Template_Name>Coagulation factor VIII</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selections, IgGs from FVIII inhibitor-positive plasma was immobilized on streptavidin-coated beads via a biotin-conjugated goat anti-human IgG. For negative selections, IgGs from a plasma pool of healthy individuals negative for FVIII-specific antibodies were immobilised likewise.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2890</BiopanningDataSetID>
<Peptides>DAWIGSRIPFKG(14)
LCLDISCHIPTK(2)
SHSAIQDHMPRK(1)
RTWHPSEIMHEY(1)
VHMKQIPSWLIK(1)
LDKQTLKYLHEK(1)
VEGIAGHIPTKL(1)</Peptides>
<Motif>I-x(2)-[HR]-[ILM]-P-x-K</Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:25520269</Reference>
<Target_Name>Anti-coagulation factor VIII polyclonal antibody IgG from haemophilia A patient 10</Target_Name>
<Template_Name>Coagulation factor VIII</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selections, IgGs from FVIII inhibitor-positive plasma was immobilized on streptavidin-coated beads via a biotin-conjugated goat anti-human IgG. For negative selections, IgGs from a plasma pool of healthy individuals negative for FVIII-specific antibodies were immobilised likewise.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2891</BiopanningDataSetID>
<Peptides>GIIIPHQ[0.95 ± 0.04]
MIPHDEN[1.16 ± 0.04]
VHALVPH[0.85 ± 0.05]
FSLIPHS[1.01 ± 0.09]
ISLIPHT[1.03 ± 0.08]
FVPHANK[0.95 ± 0.04]
IMPLWPH[0.84 ± 0.04]
LIPHDSL[1.19 ± 0.02]
LNPNKLI[0.81 ± 0.05]
WNLVPHT[0.88 ± 0.04]</Peptides>
<Motif>[IV]-P-H-D</Motif>
<Unique_Sequence_Number>10</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:25741007</Reference>
<Target_Name>Anti-avian hepatitis E virus (HEV) capsid protein monoclonal antibody 3E8</Target_Name>
<Template_Name>Capsid protein</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method>ELISA</Affinity_Measurement_Method>
<Affinity_Measurement_Description>Affinities of phages to mAb 3E8 were measured by phage ELISA. The OD values at 490 nm were measured and data shown were reproduced from the Fig. 2A in the reference. Error bars indicate the standard range of individual values from two independent experiments and the results were presented as mean ± standard deviation.</Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2892</BiopanningDataSetID>
<Peptides>KLAPHAN[1.07 ± 0.13]
GLKLYQS[1.68 ± 0.06]
FKLYMEP[1.63 ± 0.04]
VKLYMTF[1.81 ± 0.04]
VHALYLQN[0.96 ± 0.02]
LDPARF[1.09 ± 0.15]
GNLFMTL[1.43 ± 0.07]
VKLFMSTL[1.73 ± 0.05]
RDAVRPF[1.25 ± 0.03]</Peptides>
<Motif>V-K-L-Y-[MT]-S</Motif>
<Unique_Sequence_Number>9</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:25741007</Reference>
<Target_Name>Anti-avian hepatitis E virus (HEV) capsid protein monoclonal antibody 1B5</Target_Name>
<Template_Name>Capsid protein</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method>ELISA</Affinity_Measurement_Method>
<Affinity_Measurement_Description>Affinities of phages to mAb 1B5 were measured by phage ELISA. The OD values at 490 nm were measured and data shown were reproduced from the Fig. 2B in the reference. Error bars indicate the standard range of individual values from two independent experiments and the results were presented as mean ± standard deviation.</Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2893</BiopanningDataSetID>
<Peptides>RATQLPQ(4/12)
QHIPKPP(2/12)
HRRPSRS(1/12)
AFDTHTM(1/12)
TPPEPAP(1/12)
NQDVPLF(1/12)
HRLRISP(1/12)
GDTQRVA(1/12)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:25947144</Reference>
<Target_Name>δ2 CDR3 peptide CACDVLGVNTDKLIFGKG</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-7 phage display library (X7)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>Four peptides that bound to the predominant δ2 CDR3 fragments and showed homology to M.tb genes in a BLAST search. Notably, one fragment was related to M.tb H37Rv (QHIPKPP), and this fragment was confirmed as a ligand for the γδ TCR.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2894</BiopanningDataSetID>
<Peptides>SEISAST(2/10)
ATKTRQP(2/10)
LNPVHRL(1/10)
YPTGLPL(1/10)
RFRPTPP(1/10)
ADHPPPH(1/10)
SRVRLGA(1/10)
HRSHSTH(1/10)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:25947144</Reference>
<Target_Name>δ2 CDR3 peptide CACDTLGDRDYTDKLIFGKG</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-7 phage display library (X7)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2895</BiopanningDataSetID>
<Peptides>GWHHHPR(5/12)
HKRPRNN(1/12)
HRRPSRS(1/12)
RRRPMAI(1/12)
HGSTKRT(1/12)
WNPHKHH(1/12)
WRQTRKD(1/12)
GTTTTLL(1/12)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:25947144</Reference>
<Target_Name>δ2 CDR3 peptide CACDTIGTGGHYTDKLIFGKG</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-7 phage display library (X7)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2896</BiopanningDataSetID>
<Peptides>SPRVGAT(2/13)
ATKTRQP(1/13)
HKRPRNN(1/13)
AFDTHTM(1/13)
SEISAST(1/13)
QHIPKPP(1/13)
RRAPTPP(1/13)
YMQLPSH(1/13)
KLAPMTS(1/13)
GWHHHPR(1/13)
ASPDTPQ(1/13)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>11</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:25947144</Reference>
<Target_Name>δ2 CDR3 peptide CACDTLWGIQGNTDKLIFGKG</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-7 phage display library (X7)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2897</BiopanningDataSetID>
<Peptides>TDFNTMAKNNPP[4.97]</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:26040578</Reference>
<Target_Name>Biotinylated anti-lysozyme polyclonal antibody IgG</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method>ELISA</Affinity_Measurement_Method>
<Affinity_Measurement_Description>Binding capabilities of the selected phage toward biotinylated anti-lysozyme polyclonal antibody IgG was estimated by ELISA. The absorbances at 418 nm were measured and data shown were reproduced from the Fig. 4 in the reference. The affinity value was 4.97 when the biotinylated anti-lysozyme polyclonal antibody IgG was at a concentration of 3e-8.</Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2898</BiopanningDataSetID>
<Peptides>STGTPRA(3)
KSTSQPE(2)
TRTPQHS(1)
LSTRAPL(1)
DRAPGRT(1)
LSPARTT(1)
PPYLSTR(1)
TTTPTLH(1)
TMTGSTT(1)
PYSAKAH(1)
PPYLSHL(1)
RPAPNQT(1)
PHPISKQ(1)
TNTAWTS(1)
MTSSGML(1)
HHTTSTG(1)
ISQPIRQ(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>17</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:25802296</Reference>
<Target_Name>Biopolymer transport protein ExbD (43–141)</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2899</BiopanningDataSetID>
<Peptides>FSISTLQSAPTR(2)
QTTAWWGAPARL(2)
QMMQTSSSPPTV(1)
STNPAALYSDYS(1)
HHRAHNSHLSVR(1)
HSIFYPIYLPSQ(1)
FHESWPSPAGGR(1)
FPHYPVSTLYSL(1)
STPQPSLFSYPV(1)
FHSSTPTAPPQK(1)
NGLTSSRPWSFL(1)
SPIYVTWVPTAL(1)
NDPGRLRVPVST(1)
RHYEPLSRVSSS(1)
STPQVYNVFYAP(1)
FHSHWPSMADNS(1)
TVYWITPPALPI(1)
FHETWPARVSYL(1)
SHHWEPISSPLR(1)
KIYPITLTYLAP(1)
SSKVLPSSFFTR(1)
APTTQTPPINWK(1)
QTNSQHPISALR(1)
RHSEPISVFYIT(1)
HPIYVTYYPDPS(1)
HLLMKPPQTSPA(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>26</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:25802296</Reference>
<Target_Name>Biopolymer transport protein ExbD (43–141)</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2900</BiopanningDataSetID>
<Peptides>SHSNTTQTRPSD
SHALPLTWSTAA
NTIPMHTSTHTI
IHPASQSRQNTT
AALGTYSTHTPT
HLPTSSLFDTTH
HGLPVTTRGAFG
TKTVAQTTTSIS
KLVDESSTSPLS
HSNLPTKRPTSL</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>10</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:25802296</Reference>
<Target_Name>Protein TonB (33-239)</Target_Name>
<Template_Name>Ferrienterobactin receptor</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item></BiopanningDataSet></result>