<result><BiopanningDataSet><Item><BiopanningDataSetID>2276</BiopanningDataSetID>
<Peptides>ATSLPPTEHPNMYQG(1)
AGGYSPTEHAFHSPP(1)
TSTPTEHTYPLEIIT(1)
DPGTEHAGVPLRHSA(1)
YGARPPEHLLYSRAS(1)
SPLPEPPPEHRALVP(1)
YMQPDPPPPLHAPDY(1)
TRMPLPNHYEPPPRT(1)</Peptides>
<Motif>PPPEH</Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:10423148</Reference>
<Target_Name>Anti-gG2 monoclonal antibody E5</Target_Name>
<Template_Name>Envelope glycoprotein G, gG, gG-2</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>f88-15mer phage display library (X15)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>After three rounds of biopanning, individual phage clones were isolated and screened by ELISA to identify those which bound strongly to the antibody of interest, and those which gave a clear positive signal were sequenced. </BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2277</BiopanningDataSetID>
<Peptides>ALSSQGGMSPEPTPL(2)
VSSRPTTHYYLPEPL(1)
TPESTPLLPPFPRSV(1)
STNPEPLPFPAEELS(1)
QKYAPETTPVSYLGA(1)
HVLSSRPTTLALPLF(1)
DYTPQTSLELPPESF(1)
TPAQAYPALRSLIPW(1)
TATTVTPRRTPYAPI(1)</Peptides>
<Motif>TPL</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:10423148</Reference>
<Target_Name>Anti-gG2 monoclonal antibody F11</Target_Name>
<Template_Name>Envelope glycoprotein G, gG, gG-2</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>f88-15mer phage display library (X15)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description> </Brief_Description>
<BiopanningDataSet_Comments>After three rounds of biopanning, individual phage clones were isolated and screened by ELISA to identify those which bound strongly to the antibody of interest, and those which gave a clear positive signal were sequenced.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2278</BiopanningDataSetID>
<Peptides>QPTSKPTRPWLVSFL(1)
NAETAFSLSSFPPSP(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>2</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:10423148</Reference>
<Target_Name>Anti-gG2 monoclonal antibody H7</Target_Name>
<Template_Name>Envelope glycoprotein G, gG, gG-2</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>f88-15mer phage display library (X15)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>After three rounds of biopanning, individual phage clones were isolated and screened by ELISA to identify those which bound strongly to the antibody of interest, and those which gave a clear positive signal were sequenced.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2279</BiopanningDataSetID>
<Peptides>RGRGAG
LGRRRS
IRGRWA
AGRSAF
GRTDFW
IKRNIT
PRGRGG
NKYARQ
YHIKRS</Peptides>
<Motif>[GA]-R-x-[AG]</Motif>
<Unique_Sequence_Number>9</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>1</Rounds_of_Panning>
<Reference>PMID:7644467</Reference>
<Target_Name>Tissue-type plasminogen activator</Target_Name>
<Template_Name>Plasminogen, EC=3.4.21.7</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>f3-6mer phage display library (X6)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selection, the phage library was digested overnight at 37°C by concentrations of t-PA varying from 10 to 100 μg/ml. The reaction mixture was then placed on ice, bovine serum albumin was added to 0.1%, and 100 μg of mAb 179 and 10 μg of mAb 3-E7 were added. After 30 min on ice, 100 μl of Pansorbin cells was added, and the reaction mixture was rotated at 4°C for 1 hr. The mixture was microcentrifuged for 2 min, and the supernatant was recovered to repeat the Pansorbin adsorption. </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2280</BiopanningDataSetID>
<Peptides>VLRSAR
QYLRYG
KDARRA
WLPRRA
ILRAAY
LRGRTA</Peptides>
<Motif>[GA]-R-x-[AG]</Motif>
<Unique_Sequence_Number>6</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>2</Rounds_of_Panning>
<Reference>PMID:7644467</Reference>
<Target_Name>Tissue-type plasminogen activator</Target_Name>
<Template_Name>Plasminogen, EC=3.4.21.7</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>X6 fAFF1-tether C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selection, the phage library was digested overnight at 37°C by concentrations of t-PA varying from 10 to 100 μg/ml. The reaction mixture was then placed on ice, bovine serum albumin was added to 0.1%, and 100 μg of mAb 179 and 10 μg of mAb 3-E7 were added. After 30 min on ice, 100 μI of Pansorbin cells was added, and the reaction mixture was rotated at 4°C for 1 hr. The mixture was microcentrifuged for 2 min, and the supernatant was recovered to repeat the Pansorbin adsorption. </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2281</BiopanningDataSetID>
<Peptides>GFARRA
FGRRRT
TRARRA</Peptides>
<Motif>[GA]-R-x-[AG]</Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:7644467</Reference>
<Target_Name>Tissue-type plasminogen activator</Target_Name>
<Template_Name>Plasminogen, EC=3.4.21.7</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>X6 fAFF1-tether C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selection, the phage library was digested overnight at 37°C by concentrations of t-PA varying from 10 to 100 μg/ml. The reaction mixture was then placed on ice, bovine serum albumin was added to 0.1%, and 100 μg of mAb 179 and 10 μg of mAb 3-E7 were added. After 30 min on ice, 100 μI of Pansorbin cells was added, and the reaction mixture was rotated at 4°C for 1 hr. The mixture was microcentrifuged for 2 min, and the supernatant was recovered to repeat the Pansorbin adsorption.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2282</BiopanningDataSetID>
<Peptides>QRGRKA
IVRRAE
VARRAA</Peptides>
<Motif>[GA]-R-x-[AG]</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:7644467</Reference>
<Target_Name>Tissue-type plasminogen activator</Target_Name>
<Template_Name>Plasminogen, EC=3.4.21.7</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>X6 fAFF1-tether C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selection, the phage library was digested overnight at 37°C by concentrations of t-PA varying from 10 to 100 μg/ml. The reaction mixture was then placed on ice, bovine serum albumin was added to 0.1%, and 100 μg of mAb 179 and 10 μg of mAb 3-E7 were added. After 30 min on ice, 100 μI of Pansorbin cells was added, and the reaction mixture was rotated at 4°C for 1 hr. The mixture was microcentrifuged for 2 min, and the supernatant was recovered to repeat the Pansorbin adsorption. </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2283</BiopanningDataSetID>
<Peptides>FTGRDI
GFARAA
IGRRAQ
KAIGRM
LGRKAT
LKGRRA
MRGRRG
MRLRRA
PFGRSA
PYSRMA
QLGRKA
RGRRAR
RGRSAG
RRGRRA
RYARRL
RYARSA
SRARKA
SYLRRA
TFARRA
TVMRRA
VARRAA
WLGRRG
YIGRRG</Peptides>
<Motif>[GA]-R-x-[AG]</Motif>
<Unique_Sequence_Number>23</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:7644467</Reference>
<Target_Name>Tissue-type plasminogen activator</Target_Name>
<Template_Name>Plasminogen, EC=3.4.21.7</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>X6 fAFF1-tether C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For positive selection, the phage library was digested overnight at 37°C by concentrations of t-PA varying from 10 to 100 μg/ml. The reaction mixture was then placed on ice, bovine serum albumin was added to 0.1%, and 100 μg of mAb 179 and 10 μg of mAb 3-E7 were added. After 30 min on ice, 100 μI of Pansorbin cells was added, and the reaction mixture was rotated at 4°C for 1 hr. The mixture was microcentrifuged for 2 min, and the supernatant was recovered to repeat the Pansorbin adsorption.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2284</BiopanningDataSetID>
<Peptides>MGTTHLPYQFSL(3)</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:24040227</Reference>
<Target_Name>Listeria monocytogenes serotype 4b</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>2285</BiopanningDataSetID>
<Peptides>KQATFDDYPVAH(7)
MGTTHLPYQFSL(2)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>2</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:24040227</Reference>
<Target_Name>Listeria monocytogenes serotype 4b</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>The first three surface biopanning rounds were performed against L. monocytogenes to select for phages binding to  L. monocytogenes. The fourth included an initial subtraction biopanning step performed against L. innocua  and using the supernatant derived from that for the subsequent biopanning against L. monocytogenes.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2286</BiopanningDataSetID>
<Peptides>KQATFDDYPVAH(3)
KLHISKDHIYPT(2)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>2</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:24040227</Reference>
<Target_Name>Listeria monocytogenes serotype 4b</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>One solution biopanning was performed following the completion of the third surface biopanning round. The first three surface biopanning rounds were performed against L. monocytogenes to select for phages binding to L. monocytogenes. The solution biopanning included one solution biopanning against viable L. innocua and one against viable L. monocytogenes 4b.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2287</BiopanningDataSetID>
<Peptides>GPLATLHLPHKT(2)</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:24040227</Reference>
<Target_Name>Listeria monocytogenes serotype 4b</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>Two solution biopannings were performed following the completion of the third surface biopanning round. The first three surface biopanning rounds were performed against L. monocytogenes to select for phages binding to L. monocytogenes. Each solution biopanning round included one solution biopanning against viable L. innocua and one against viable L. monocytogenes 4b.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2288</BiopanningDataSetID>
<Peptides>ANAGPIMTTSLL(1)
G*V*KPPQNVNR(1)
GAKHPAQPHMMY(1)
GAMHLPWHMGTL(3)
GAMHLSVAYGYA(1)
GEVDFNPR*DCA(1)
GIIYDNPRKELN(1)
GIIYSRGPEKLL(1)
GIIYTLPAARYD(1)
GIVFTLPALAHN(2)
GKLFSSLDGL*F(1)
GKLFSSPMDYDS(4)
GKLYSHPLNNAK(5)
GLLWTHPQTHGR(18)
GMIWNEPKTWPG(1)
GMIYVKPARPML(1)
GNLFASPQKMHR(12)
GPIFSAPT*TTI(1)
GPIFSNSWGLIT(2)
GPIFVNSDKGER(1)
GPIHVAAFKNMT(1)
GPILDMGFFNRE(1)
GPIMSLPHRTVG(1)
GPIMSLPTPTNL(1)
GPINSKPSHMHI(1)
GPIRDIGPVMDH(3)
GPIVDSGGTHPR(1)
GPIVSMPMPRLL(1)
GPIWDNMPSRQV(1)
GPIWSGRLIAQD(1)
GPIYETIKTRTP(1)
GPIYQQQNTILR(1)
GPIYSTQHMKTS(3)
GPLFDQGTQAYA(2)
GPLHSSPLKISS(2)
GPLISTPRHMNI(4)
GPLVDLGPGDLR(6)
GPLWTGQSQGSP(1)
GPLYESRMPQNH(2)
GPLYISSLTQLA(1)
GPLYIVSHDTPR(1)
GPVHSHPNDYSR(2)
GQVYDVPYSRPK(2)
GRIADLPPLKPN(3)
GRIATLPDPTPR(2)
GTDLD*AAAS*A(1)
GTIFDYGPHGYA(1)
GTIFDYGPPDMP(13)
GTIWSQPGAISL(1)
GVIWSDPKTASS(1)
GVIYDKPA*KLH(11)
GVIYDSHGPGRY(1)
GVIYSKPNSVQL(7)
GVIYSSDRDWRS(1)
GVIYTDSLTRPH(1)
GVMCKHPQTHGH(1)
KLHISKDHIYPT(6)
KQATFDDYPVAH(5)
LYAKKPLLNPNR(2)
NRPDSAQFWLHH(4)
QSWPAAA*AFTS(1)
TSMDSVSVIDLG(1)
TSSQGDRLYVYK(2)
TSWPSLSTSARS(1)
VNLEHGYYHAPS(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>65</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:24040227</Reference>
<Target_Name>Listeria monocytogenes serotype 4b</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>Two solution biopannings were performed following the completion of the third surface biopanning round. The first three surface biopanning rounds were performed against L. monocytogenes to select for phages binding to L. monocytogenes. Each solution biopanning round included one solution biopanning against viable L. innocua and one against viable L. monocytogenes 4b.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2289</BiopanningDataSetID>
<Peptides>ANATFHGYPTRS(1)
FFPREYYSIEAP(1)
GGNGPKGNNVVH(1)
GKIWTEPPPPKP(1)
GKIYNDPRMMSN(1)
GKLFSSPMDYDS(1)
GKLYSHPLNNAK(2)
GKYHEKHNENMH(1)
GLIWDLSWCSSK(1)
GLLWTHPQTHGR(1)
GMIWNEPKTWPG(1)
GMIWSRPSAEKF(1)
GNLFASPQKMYR(2)
GPIATLPKGGGQ(1)
GPIFSNSWGLIT(5)
GPIHEAPSSPSG(2)
GPIIA*TYPKRE(1)
GPILDMGFFNRE(1)
GPIMSLPHRTVG(1)
GPIWSSIQTLPT(1)
GPIYSSVKDGQR(1)
GPIYSTQHMKTS(1)
GPIYTDKSELGN(1)
GPLATLHLPHKT(1)
GPLFDQGTQAYA(1)
GPLFITSAPPTK(1)
GPLFSDPEPAKN(1)
GPLISTPRHMNI(1)
GPLVDLGPGDLR(1)
GPLWTGQSQGSP(3)
GPLYESRMPQNH(1)
GPLYESSQVIRA(1)
GPLYSSMASALA(1)
GPLYSTNLPTRN(2)
GPLYSYPFSMIE(1)
GPSHNTLSPLLT(1)
GPVHSHPNDYSR(1)
GPVLDPLTPSTI(1)
GQIYTTRDSLLG(1)
GQKPT*NLDLKL(1)
GQVYDVPYSRPK(2)
GSIYAHPRWLKW(1)
GTIMTLANTERP(1)
GTIQVHPPAPAR(1)
GVIWSDPKTASS(1)
GVIYSKPNSVQL(1)
GVIYSSDRDWRS(1)
GVIYSTHDTRPY(1)
GVLHSSPNHRWQ(1)
GWHKHKSMSAPL(1)
HLINTNAQIAQR(1)
IQLEMGGTRFHR(2)
KDDASPAWNSRH(1)
KHMMINAYRMTE(1)
KIHKTESTPAWF(1)
KKGDV**L*LRR(1)
KLHISKDHIYPT(4)
KNLHVGSYPQPI(1)
KPHAHKHNDYFL(1)
KPHHPHKIPYTN(1)
KPHNMTELHHKH(1)
KPHYDHRLHQPI(1)
KQATFDDYPVAH(24)
KQSDVR*VSWWA(1)
KRRAKQKTGEQR(1)
LDLQTPGHKWSQ(1)
LLPPT*ATVGAR(1)
LSCTTSVACLQT(1)
NVATKSSGHNMR(1)
RQVRMHPLDSWS(1)
RRKMKQTEKMKI(1)
SKSRAKGKQAKN(1)
SLNRKKRRTHAK(1)
SLRQVNTHTWLT(1)
TDAKMRAKFPGH(1)
TQARCNEYPVGH(1)
TSMDSVSVIDLG(1)
VNLEHGYYHAPS(3)
VNLQTGWYTMAS(7)
VNSADWVVCDGV(1)
VSLPMGFYSMNS(1)
YLPISQTHNRNV(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>82</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:24040227</Reference>
<Target_Name>Listeria monocytogenes serotype 4b</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>One solution biopanning was performed following the completion of the third surface biopanning round. The first three surface biopanning rounds were performed against L. monocytogenes to select for phages binding to L. monocytogenes. The solution biopanning included one solution biopanning against viable L. innocua and one against viable L. monocytogenes 4b.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2290</BiopanningDataSetID>
<Peptides>CIQTTWSRC</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:15987688</Reference>
<Target_Name>Amyloid β peptide, Aβ40</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>Thirty Aβ40 -binding clones were individually picked, amplified, and had their DNA sequenced. Most of the 30 clones thus obtained had different DNA sequences. The IQ peptide (CIQTTWSRC) may be a lead for the development of novel drugs to block the inhibition of nAChRs in AD.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2291</BiopanningDataSetID>
<Peptides>RRWVRYPVHLHSPIV(1)
PPYHRFWRGHRHAVQ(12)
HRISHFAHRYLARLH(2)
WHWRHRIPLQLAAGR(2)
GWHSLLHSRYHRIAA(1)
FVWVRFHRLPRQIYT(1)
WHKYFLRRPLSVRTR(4)
VPMALNHGVYVMVSS(1)
RKWFLQHRRMPVSVL(6)
SGRRHLHRHHIFSLP(2)
GWITFHRRHHDRVLS(1)
RLHGHRSHRFTHVAQ(1)
KRIWFIPRSSWYERA(3)
MPLSRYWWLFSHRPR(1)
RHLSHFKWLRSHGLD(1)
RRFHFHSRMVAVDNS(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>16</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:17804251</Reference>
<Target_Name>Transforming growth factor beta-1, TGF-beta-1</Target_Name>
<Template_Name>Transforming growth factor beta receptor type 3, TGF-beta receptor type 3, TGFR-3</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>f5-15mer phage display library (X15)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Each selection was performed on the streptavidin-coated plates.</Brief_Description>
<BiopanningDataSet_Comments>In vitro and in vivo experiments were performde to valuate their capacity to neutralize TGF???21. A murine model of acute liver damage was used to test the in vivo activity of all 20 phage-derived peptides. As found in vitro, P17 (KRIWFIPRSSWYERA) was also the most active in vivo followed by P6 (PPYHRFWRGHRHAVQ), P4 (RLAHSHRHRSHVALT), P14 (SGRRHLHRHHIFSLP) and P11 (WHKYFLRRPLSVRTR). Other peptides such as P1 (DRRIFWWSLRSAPGA), P3 (RFFTRFPWHYHASRL), P7 (HRISHFAHRYLARLH), P9 (GWHSLLHSRYHRIAA), P15 (GWITFHRRHHDRVLS), P19 (RHLSHFKWLRSHGLD) and P13 (RKWFLQHRRMPVSVL) were without effect on the expression of collagen type I mRNA whereas peptides, P2 (HVRLHHYLRHRSLPN), P5 (RRWVRYPVHLHSPIV), P8 (WHWRHRIPLQLAAGR), P10 (FVWVRFHRLPRQIYT), P12 (VPMALNHGVYVMVSS), P16 (RLHGHRSHRFTHVAQ) and P18 (MPLSRYWWLFSHRPR) enhanced expression of collagen type I mRNA.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2292</BiopanningDataSetID>
<Peptides>CRMSRRSNC
CMRNRPKRC
CRRRLNRTC
CRMRIRRNC
CHPHPRPRC</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>5</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:20428769</Reference>
<Target_Name>Anti- FASN monoclonal antibody K1</Target_Name>
<Template_Name>Fatty acid synthase, EC=2.3.1.85</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>A mimotope CMRNRPKRC against anti-FASN autoantibody can be used as an efficient diagnostic method of HCC.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2293</BiopanningDataSetID>
<Peptides>GNLFGRD(1)
LSFPDWP(2)
HSWLPYL(1)
YSWTPH(1)
QVLMMRP(2)
YLIPPGL(1)
FTPPVTL(1)
TYLPGPL(1)
TVSPGMK(1)
DPPREIS(1)
WHQTVPF(1)
SISFWTL(1)
IAKPGFW(1)
WPKFHPS(1)
GSSLDDS(1)
SHLAPAL(1)
TQSLSPP(1)
IPLPQSP(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>18</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:23845304</Reference>
<Target_Name>Anti-PCV2 Cap polyclonal antibody</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.-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>2294</BiopanningDataSetID>
<Peptides>VTAMEPGQ(28)
AFNPEPGQ(11)
VTALEPGQ(7)
DTPPGWDQ(5)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>4</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:23885226</Reference>
<Target_Name>Rat mesenchymal stem cells, rMSCs</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>fd-tet X8 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>The landscape phage library was first depleted with culture flask to remove the phages that specifically bound to the culture flask. The depleted phage library was then incubated with target rMSCs.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2295</BiopanningDataSetID>
<Peptides>YEQDPWGVKWWY(8)
HLSWLPDVVYAW(2)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>2</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:24046373</Reference>
<Target_Name>M2 macrophages</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 and Ph.D.-C7C phage display library pool</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>For the subtractive pans, 2.0e11 pfu of the amplified eluate was first applied to receptor-cleared M1 cells. M1 cells were centrifuged, and the supernatant was applied to M2 cells. Phage was eluted from M2 cells and amplified. Subtractive panning was repeated three times, using the amplified eluate from the previous pan as the starting library for each round.</Brief_Description>
<BiopanningDataSet_Comments>M2pep (YEQDPWGVKWWY) shows selective binding and internalization in M2 macrophages but with minimal M1 macrophage interaction. We demonstrate this peptide's ability to identify murine M2-like TAMs within mixed cell populations isolated from mouse colon carcinoma tumors and to accumulate in TAMs after i.v. injection into tumor-bearing mice. We show that i.v. administration of M2pep fusion peptides with KLAKLAKKLAKLAK (KLA), a proapoptotic peptide, to tumor-bearing mice selectively reduces TAM populations and prolongs survival.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2296</BiopanningDataSetID>
<Peptides>NQYMSNGLVWAL(1)
GDWPAGQMARSA(1)
SPWSPPFWNDDM(1)
QGPQTDSAPPRF(1)
GFNTNPPSFPRP(1)
GPLKAYILPPKA(7)
AAHQPPAQSDFL(1)
WSAPGLSSSSAP(1)
LSSSAVTNNTSS(1)
DSPTVAHNTSPT(1)
HETVQHNKGWMI(1)
IEHNGKAWRIPQ(1)
EVAAFSMPGRFS(1)
YVEPQEQSMPYL(1)
NIQLELNPRHLI(1)
SNSTREFNPNMF(1)
HHQNTYANYPRH(2)
WPHHHSRHNHNH(1)
STHGWMNDRHHP(1)
KSITSNDGFNTL(1)
GSITTQTAIYFP(1)
LTSAISPQHGEY(1)
SHSFHTQERTTH(1)
AVFSQLPRTPHL(1)
SLPEAPIRQYQG(1)
HVTMSWPQTAQN(1)
SNAGGLMSRTWE(1)
KIMPDSWAIKPW(1)
NVMIDKHNVNGS(1)
DSYMHAYSWRTK(1)
SFQNSTLHGPVY(1)
HIGHDNHLYPNR(1)
NARVLHTGNESL(1)
DRAMTPIYNPYI(1)
TYTDNGYFKRST(1)
TATIKSEAKSPS(1)
YVEQVSTGKARS(1)
RTRMRSINSPNL(1)
SYYGKTDTADLT(1)
VVDIRSQFANQQ(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>40</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:24039747</Reference>
<Target_Name>Bacteriorhodopsin, BR</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>2297</BiopanningDataSetID>
<Peptides>KVWSVPQLSHQL(1)
KVWLLETSHISL(1)
KLWYLNPPPGSF(2)</Peptides>
<Motif>K-[VL]-W</Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:24039747</Reference>
<Target_Name>Nanodiscs</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>2298</BiopanningDataSetID>
<Peptides>MQLPKADARHPH
YQITLPYRYEMP
TFSWEFTGWWGQ
LTFPVTTTPPAV
MTHNMHGPNSEP
HALTPIKYIPPG
SSAYYYHYEYFH
LSISPQHALVFA
AMYHGHYTITRW</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>9</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3-6</Rounds_of_Panning>
<Reference>PMID:23830854</Reference>
<Target_Name>Membrane protein, M protein</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>To determine the impact of pepTGEV-M7 (HALTPIKYIPPG) on TGEV infection, three separate approaches were used: (1) TGEV was treated with peptide before inoculation of ST cells; (2) ST cells were treated with peptide prior to TGEV inoculation, and; (3) ST cells were infected with TGEV before being treated with peptide. These results indicate that pepTGEV-M7 is able to interfere with the ability of the virus to infect ST cells. The antiviral effects of pepTGEV-M7-treated virus were further investigated by IFA. Results demonstrated a dosedependent reduction in the infection of ST cells in the presence of pepTGEV-M7.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2299</BiopanningDataSetID>
<Peptides>NRPDSAQFWLHH
YSAQFPLYTSWS
WSEYDIPTPQIP
GNLFASPQKMYR
LNQSPQLQNKYR
STFAGHVMTSVQ
FPIKDPSNTFQY
DFPISYRSWQIS
RYWDTQLSPQML
YQLQLPVWNDWA
NMSHEMQLYALA
WQLQLPVWSSSD
ENMIVRLQSFQR
EFFQYWEHIMWF
NEPDFYAWQHFM
WMWPSHMQEFSW
VPFNWHWMQHYD
YTVMDLQDYYSP
GQLYMWMGLPIN
QTTQAQTMLHHV
SPPSTRVQNTAL
QDWQQGSRVLWL
TDYNLWTRAQFI
WSSSAMQTIQTA
MPAWEGPAQIQS
MQRDNGPHKTLR
FQCLRIPCVYAW
ETWYSEQPWSML
MLAHPSIYSSQP
QFQWWYYSDQSE
THWAKVSTDQHQ
RIGTRRESKQNE
QLPVRIQGNYLA
LQQTYLKNPRSG
MHDEVSVHQSHV
NAHQKHAGAGAR
QMAMRAHTEGKN
YTSNTQSFTSSL
WSFELPEQLFRG
WDLTQRQRDLYF
ANMEHTKHVTQA
DKPGYMLLDSQP
WRCRIELLMHQD
STPSLLFYQVES
QSTWWEIAGYTP
MPNRPWIGILAG</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>46</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:23876241</Reference>
<Target_Name>Protein-glutamine gamma-glutamyltransferase Z</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>2300</BiopanningDataSetID>
<Peptides>LGCDDTAVAHWPWVY
SDAYDTAVAHWPGFI
MPPNLIANYESALSR
YESPGFLLSGYDDTG
WAAHPSGPSIVPRSL</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>5</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>2</Rounds_of_Panning>
<Reference>PMID:23939045</Reference>
<Target_Name>Anti-SMN monoclonal antibody MANSMA1-21</Target_Name>
<Template_Name>Survival motor neuron 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>f88-15mer phage display library (X15)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>Three of these 22 mAbs were responsible for the selection process. These mAbs included two of the mostly widely-used for SMA studies, MANSMA1 and MANSMA12, and one mAb against the proline-rich region encoded by exon 5, MANSMA3. Biopanning with the remaining 19 anti-SMN mAbs alone failed to select any further phage clones.</BiopanningDataSet_Comments>
</Item></BiopanningDataSet></result>