<result><BiopanningDataSet><Item><BiopanningDataSetID>1351</BiopanningDataSetID>
<Peptides>CTESAPYFC(1)
CPDANNGNC(1)
CNMAQTNMC(1)
CPNANLGTC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>4</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Intact matrices (Integra ®)</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>The blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1352</BiopanningDataSetID>
<Peptides>CINSFYAQC(1)
CKSAISSSC(1)
CVPQYSSQC(1)
CQPKAVNHC(1)
CPVSPSGAC(1)
CSNASRPFC(1)
CNPALSTHC(1)
CGKAGLPLC(1)
CPTHPPFQC(1)
CESSAIRYC(1)
CNNGTSRLC(1)
CPSQTHPTC(1)
CTNQQRHTC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>13</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Intact matrices (Integra ®)</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>The blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1353</BiopanningDataSetID>
<Peptides>CPPTPLSLC(1)
CINASKPLC(1)
CNRMVQPMC(1)
CNLALTQAC(1)
CQEPRSNAC(1)
CPSHHLESC(1)
CNPLHRQHC(2)
CSKTFPVRC(1)
CFKHSSHQC(3)</Peptides>
<Motif></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:21329515</Reference>
<Target_Name>Solubilized matrices (Integra ®)</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>The blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1354</BiopanningDataSetID>
<Peptides>CFKHSSHQC(2)
CTYPFHASC(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:21329515</Reference>
<Target_Name>Solubilized matrices (Integra ®)</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>The blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with acid/salt were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1355</BiopanningDataSetID>
<Peptides>CLSTSSKSC(9)
CQTSANTQC(1)
CGVPAGSTC(1)
CLATKLHNC(1)
CDGVSTKHC(1)
CIKNPTKYC(1)
CMPSPSLKC(1)</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:21329515</Reference>
<Target_Name>Solubilized matrices (Integra ®)</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>The blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with glaycosaminoglycan (GAG) were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1356</BiopanningDataSetID>
<Peptides>HWHDWMWSWRRD(2)
SMWPWYYSQWAR(1)
TLGDRYSTKHPI(1)
SFSTMNTAPGGS(1)
WYMPWWSAGQAA(2)
QKKIRKRPHVKR(1)
GAFHKHHHARLI(1)
WNRSPLPDYGAA(1)
SLWQRWFPVLDH(1)
DLALRNPTPSDP(1)
SHALPLTWSTAA(1)
WHYNSWYRWPVM(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>12</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Solubilized matrices (Integra ®)</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 blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1357</BiopanningDataSetID>
<Peptides>AYYPQNHKSNAE(2)
APQYQHNQATHT(1)
SITWTHHPGALQ(1)
AGLHPRSLESLP(1)
HPGNRSLDPLNH(1)
LLADTTHHRPWT(1)
ATGKPTRLESHV(1)
NPSNLYRQPAMT(1)
SKAHDISQRQPP(1)
VNRIPGENLSSP(1)
SNQPAPALFHQL(1)
YSPASKSPVPSL(1)
SVSVGMKPSPRP(2)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>13</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Solubilized matrices (Integra ®)</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 blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with glaycosaminoglycan (GAG) were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1358</BiopanningDataSetID>
<Peptides>CVPSSARIC(1)
CRPHDSKAC(1)
CHPEPRSQC(1)
CVEKRPRQC(1)
CFMDYRNLC(1)
CSHSVQPFC(1)
CQTHNPRQC(1)
CDGAPAPLC(1)
CKTDLQKQC(1)
CGPFPQPHC(1)
CSFHGPGPC(1)
CSTNQTPTC(1)
CSTSPONSC(1)
CKLIHNNSC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>14</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Cryostat-sectioned matrices (Integra ®)</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>The blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1359</BiopanningDataSetID>
<Peptides>CHMSPRHQS(1)
CLPNKQWSC(1)
CKQPLNNTC(1)
CTVTPRHLC(1)
CDNTSKTQC(1)
CASTTAACC(1)
CLHMDKKRC(1)
CMKTPMRSC(1)
CYKHVGQRC(1)
CHLSPFKSC(1)
CTTSKYRDC(1)
CTATGLSNC(1)
CPSSMPSRC(1)
CPATSHTHC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>14</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21329515 </Reference>
<Target_Name>Cryostat-sectioned matrices (Integra ®)</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>The blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with acid/salt were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1360</BiopanningDataSetID>
<Peptides>CVQSSTQHC(1)
CSGHHSLRC(1)
CPTSQQKVC(1)
CNSTHPRAC(1)
CNRLESHLC(1)
CTNPHRSQC(1)
CTKTPWPGC(1)
CNRLQGEHC(1)
CPTPTGRYC(1)
CVPTAMSNC(1)
CSLARPNEC(1)
CVRTPFSMC(1)
CNNTTPPSC(1)
CTSQQKANC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>14</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Cryostat-sectioned matrices (Integra ®)</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>The blocking strategies with phosphate-buffered saline with Tween (PBS-T) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1361</BiopanningDataSetID>
<Peptides>CHVTAQRAC(1)
CATPEWPPC(1)
CPNLMNTRC(1)
CTKSSPPRC(1)
CTQTTVASC(1)
CDQSKTIAC(1)
CSRGSMGIC(1)
CSPIRGSMC(1)
CSHTGHHQC(1)
CHEPTTMAC(1)
CSRADLTTC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>11</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Cryostat-sectioned matrices (Integra ®)</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>The blocking strategies with phosphate-buffered saline with Tween (PBS-T) were deployed, and eluates treated with acid/salt were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1362</BiopanningDataSetID>
<Peptides>CKGPVSRHC(1)
CTTSSEHVC(1)
CSTTMKTSC(1)
CDNKRSPAC(1)
CKLNYPNAC(1)
CQFSKSQSC(1)
CTLDTRRDC(1)
CPFSSSPSC(1)
CPSMSHHQC(1)
CSASTQSFC(1)
CPLKGLATC(1)
CTGKPLKTC(1)
CIHMTGYHC(1)
CEMTETKHC(1)
CKENWPLIC(1)
CSNSPTTMC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>16</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Cryostat-sectioned matrices (Integra ®)</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>The blocking strategies with bovine serum albumin (BSA) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1363</BiopanningDataSetID>
<Peptides>CGKHDDTYC(1)
CPTKDLRYC(1)
CTSSGNRYC(1)
CTIKTNLQC(1)
CHSTAKSAC(1)
CPASKGDFC(1)
CSHRVPHDC(1)
CHATPYPKC(1)
CDSSRHTHC(1)
CSRLSQEYC(1)
CTGKQYPQC(1)
CGMNAFRAC(2)
CTTKYSTTC(1)
CSSDKALVC(1)
CSPRSHLSC(1)
CPPSPMPYC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>16</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Cryostat-sectioned matrices (Integra ®)</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>The blocking strategies with phosphate-buffered saline with Tween (PBS-T) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1364</BiopanningDataSetID>
<Peptides>HETFPSPRANSV(6)
SQIDYATGPRQA(1)
WDTEKASPLSPL(1)
DHTGKSPGLFHN(1)</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:21329515</Reference>
<Target_Name>Solubilized matrices (Integra ®)</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 blocking strategies with non-fat milk (NFM) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1365</BiopanningDataSetID>
<Peptides>AHKHKHPGHITA(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:21329515</Reference>
<Target_Name>Solubilized matrices (Integra ®)</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 blocking strategies with phosphate-buffered saline with Tween (PBS-T) were deployed, and eluates treated with acid were used.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1366</BiopanningDataSetID>
<Peptides>STSVLYN
THHHLPN
AFHGPVH
LPLTPLP</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:21362346</Reference>
<Target_Name>Anti-human TGF-β1 monoclonal antibody</Target_Name>
<Template_Name>Transforming growth factor beta-1, TGF-beta-1</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>The data of MTT showed that TGF-β1 and one phage model peptide (LPLTPLP) could promote keloid fibroblasts proliferation, however, other three phage model peptides could inhibit keloid fibroblasts proliferation.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1367</BiopanningDataSetID>
<Peptides>ELMAVPVPLPPA(5)
SEYTSQLIFTAT(3)
SEFSYIVIDTSL(4)
ELTAILVSPAPL(8)
ELNAQHIMEPKY(10)
ELIPMLIMQSTS(1)
EDYSTIMKTLAH(1)
STPKSPHSVASH(1)
AVQHNPTHPFYP(1)
AHSTGLSPSTLR(1)
TMSSVAPRNLSS(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>11</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21364990</Reference>
<Target_Name>Candida albicans, C. albicans</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>The peptides can distinguish C. albicans from other closely related species.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1368</BiopanningDataSetID>
<Peptides>QPHHYSL(1)
NPHSYPH(1)
QPHHYPL(1)
SPHHYPH(1)
TPHHYMH(1)
QPHHYFK(1)
WPHHFPH(1)
VPHGYFL(1)
TPHGYAH(1)
VPHSYPH(2)
QPHHYPF(1)
APHHYPM(1)
LAINIKS(1)
SPHSYPR(1)</Peptides>
<Motif>P-H-x-Y</Motif>
<Unique_Sequence_Number>14</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:21399663</Reference>
<Target_Name>Patient CA502 ascitic 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.-7 phage display library (X7)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>The library was pre-absorbed with the total immunoglobulin G (IgG) mix of 10 healthy donors to remove the phages recognized by the IgG.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1369</BiopanningDataSetID>
<Peptides>NGTTSSNNQLINENNIQN
EHMYNTPHTYHTTMKNNK
QPIHPNNM
NKLAAALE
KNYKN
TNTHN
KHTNN</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21408169</Reference>
<Target_Name>Mouse colonic dysplasia</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>X18 T7 phage display library</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>1370</BiopanningDataSetID>
<Peptides>NGTTSSNNQLINENNIQN
EHMYNTPHTYHTTMKNNK
NKLAAALE
KNYKN
TNTHN
KHTNN</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>6</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:21408169</Reference>
<Target_Name>Mouse colonic dysplasia</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>X18 T7 phage display library</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>1371</BiopanningDataSetID>
<Peptides>WHKEQFW(9)
NTWHNSR(12)
THSPGLL(1)
SINPDNR(1)
HVQLLIF(1)
SITTVAA(1)
ALLADSR(1)
EIALGAR(1)
AGPTRIS(2)
TVKTRPA(2)
ATSAIHG(1)
QTKMTNP(2)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>12</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:21418812</Reference>
<Target_Name>Purified lgG of tuberculosis serum</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>Purified IgG of health people serum was used as the molecule of counter selection during the second and third selection.</Brief_Description>
<BiopanningDataSet_Comments>Twelve phage clones with different sequences were amplified and detected with indirect ELISA and single phage HVQLLIF showed higher affinity with IgG of tuberculosis and Was identified as the positive clone.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1372</BiopanningDataSetID>
<Peptides>CPKGLDWCC(7)</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:21423621</Reference>
<Target_Name>Protein E7</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>The binding specificity and affinity of the selected peptide to HPV16E7 were tested by competitive enzyme-linked immunosorbent assay (ELISA). The antagonist peptide showed obvious anti-tumor efficacy both in cell lines and animal tumor models.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1373</BiopanningDataSetID>
<Peptides>VPQQKFR(2)
HSQISSY(1)
QPTHQLT(1)
QHQLPSD(1)
SLLSTPQ(3)
LRPTLSC(1)
LPMRPIV(1)</Peptides>
<Motif>H-x-Q, L-x-S</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:12970876</Reference>
<Target_Name>Anti-gastric cancer antigen monoclonal antibody MGb1</Target_Name>
<Template_Name>Gastric cancer antigen</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>These 10 phage clones could also partly inhibit the binding of MGb1-Ab to gastric cancer cell KATO-III.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1374</BiopanningDataSetID>
<Peptides>CHASIYDFGSC(18)
CVYALIMPPLC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>2</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:10760806</Reference>
<Target_Name>Anti-CCR5 monoclonal antibody 3A9</Target_Name>
<Template_Name>C-C chemokine receptor type 5</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>pVIII-9aa.Cys phage display library (CX9C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>All clones were tested by capture ELISA for reactivity with mAb 3A9 and 23 of 26 clones showed strong reactivity. After sequencing, 19 nonameric peptide inserts could be identified. For phage CHASIYDFGSC, the motif SIYD aligned to residues at the N terminus and FG to residues on the first extracellular loop.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>1375</BiopanningDataSetID>
<Peptides>CPHWLRDLRVC(15)
CLPPSYCFGSC(1)
CPPVFGTFTSC(1)
CYGPFSRASYC(1)
CMPPSMTSVSC(1)</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:10760806</Reference>
<Target_Name>Anti-CCR5 monoclonal antibody 5C7</Target_Name>
<Template_Name>C-C chemokine receptor type 5</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>pVIII-9aa.Cys phage display library (CX9C)</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, 64 phage clones were isolated and tested by capture ELISA for reactivity with mAb 5C7. Nineteen clones showed very strong reactivity and sequencing revealed five different phagotypes. For CPHWLRDLRVC, residues at the N terminus, first extracellular loop, and possibly the third extracellular loop could be aligned and so would contribute to the mimotope.</BiopanningDataSet_Comments>
</Item></BiopanningDataSet></result>