<result><BiopanningDataSet><Item><BiopanningDataSetID>2701</BiopanningDataSetID>
<Peptides>LLHLRL[2.89]
LALFLA[3.74]
LRQVWL[3.5]
PLALLH[3.14]
QLGLNP[3.89]
TNFMLP[3.69]
TWLGQG[3.56]
SPLTSM[2.53]
VSDVVW[3.73]</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>9</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:21666888</Reference>
<Target_Name>PDZ domain of segment polarity protein dishevelled homolog DVL-2</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>X6 M13 phage display library</Library_Name>
<Affinity_Measurement_Method>ELISA</Affinity_Measurement_Method>
<Affinity_Measurement_Description>ELISA signal/control ratio is shown.</Affinity_Measurement_Description>
<Brief_Description>The phages were propagated in the absence of IPTG to obtain medium peptide display level and allow the selection of a wider range of interacting sequences.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2702</BiopanningDataSetID>
<Peptides>CWGHSRDEC(15)
CSGGRRLEC(4)</Peptides>
<Motif>G-[HR]-[RS]-R-[DL]-E</Motif>
<Unique_Sequence_Number>2</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:16239579</Reference>
<Target_Name>Aspergillus conidium</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2703</BiopanningDataSetID>
<Peptides>CLLSATPSC(11)</Peptides>
<Motif>ATPS</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:16239579</Reference>
<Target_Name>Aspergillus conidium</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2704</BiopanningDataSetID>
<Peptides>CGGVRGLDC(6)
CSGGRRLEC(4)
CTGGRVLSC(1)</Peptides>
<Motif>G-G-R-[GR]-L-[DE]</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:16239579</Reference>
<Target_Name>Aspergillus conidium</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2705</BiopanningDataSetID>
<Peptides>CGARASGSC(5)
CARADAATC(2)</Peptides>
<Motif>G-A-R-A-[DS]-[AG]-[AS]</Motif>
<Unique_Sequence_Number>2</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:16239579</Reference>
<Target_Name>Aspergillus conidium</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2706</BiopanningDataSetID>
<Peptides>ATRDGSS(4)
SGSSIDQ(1)
GSSSGNF(1)</Peptides>
<Motif>GSS</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:16239579</Reference>
<Target_Name>Aspergillus conidium</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2707</BiopanningDataSetID>
<Peptides>DANRVGG(1)
GAIRSGL(1)
GWQGFGS(1)
SGEVGRG(1)
GGWGPGS(1)
AGSGLSN(1)
AGGQKSI(1)
TGGRVLS(1)
VGVRPDS(1)
GWHPGQE(1)
XXHAGQA(1)
EGLRRSA(1)
EYLGLAR(1)</Peptides>
<Motif>A-x-R-x-G, G-x(2)-G-x-G, A-G-x(3)-S, G-x-R-x(2)-S, H-x-G-Q, G-L-x-R</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:16239579</Reference>
<Target_Name>Aspergillus conidium</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2708</BiopanningDataSetID>
<Peptides>CRESVRDRC(1)
CNEYSRPGC(1)
CXAGPXRTC(1)
CTVDSARSC(1)
CDGRGMAC(1)
CXTRSGHXC(1)
CLEWTGLDC(1)
CATGTHGPC(1)</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:16239579</Reference>
<Target_Name>Aspergillus conidium</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2709</BiopanningDataSetID>
<Peptides>CGPIVSFGC(1)
CAGTGVSGC(1)
CGGSKVSAC(1)
CRNGSHVSC(1)
CGAAVSILC(1)
CGAVVSVDC(1)</Peptides>
<Motif>G-[AST]-x-V-S</Motif>
<Unique_Sequence_Number>6</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:16239579</Reference>
<Target_Name>Aspergillus hypha</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2710</BiopanningDataSetID>
<Peptides>CGGRLGPFC(2)
CGDRLPHFC(1)
CRSIGRLGC(1)
CPAEGSLGC(1)</Peptides>
<Motif>[GD]-[RS]-L-G</Motif>
<Unique_Sequence_Number>4</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:16239579</Reference>
<Target_Name>Aspergillus hypha</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2711</BiopanningDataSetID>
<Peptides>CVLLRSSGC(1)
CFLLRSNDC(1)
CRLWRSTGC(1)
CVPLSRSTC(1)</Peptides>
<Motif>L-x-R-S-x</Motif>
<Unique_Sequence_Number>4</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:16239579</Reference>
<Target_Name>Aspergillus hypha</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>fUSE5-based CX7C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Screening of the phage library was performed by the BRASIL method.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2712</BiopanningDataSetID>
<Peptides>RALAHPRDHPDL[1.25]
ATCSMLLSRNEA[1.11]</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:24779651</Reference>
<Target_Name>Esophageal cancer cell line Eca109</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>Phage ELISA was used to test the specific binding of the selected phage clones to Eca109 cells. Normal human esophageal epithelial cells and bovine serum albumin cells served as controls. Absorbance values at 490 nm were subsequently recorded using a plate reader. The data were reproduced from the graph.</Affinity_Measurement_Description>
<Brief_Description>Three rounds of subtractive screening of a phage peptide library were performed using Eca109 as the target cells and normal human esophageal epithelial cells as the absorber cells. For the second and third rounds of selection, the volume of added phage remained the same, yet the incubation time with the Eca109 cells decreased to 45 min and 30 min, respectively. In contrast, the incubation time with the normal esophageal cells increased to 1.25 h and 1.5 h, respectively.</Brief_Description>
<BiopanningDataSet_Comments>While ELISA, immunofluorescence and immunohistochemistry assays were used to validate the binding affinities of two positive phage clones, sequencing of the positive clones did not find any homology between the sequences obtained and a protein database.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2713</BiopanningDataSetID>
<Peptides>CKSLENSYC(18)[23.4 ± 1.1]
CKSVGNYQC(2)[3.6 ± 0.8]
CKNPTTGTC(2)[4.3 ± 0.3]
CKSLENSQC(1)[NT]
CNPSNRNDC(1)[NT]
CKSPGNYQC(1)[NT]
CKSLEQSYC(1)[NT]
CNPSNRQDC(1)[NT]
CTGTTNQYC(1)[NT]
CNSPRPSTC(1)[NT]
CNVQHNKTC(1)[NT]
CSTRHTYDC(1)[NT]
CIKSTHNHC(1)[NT]</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>13</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>6</Rounds_of_Panning>
<Reference>PMID:24841092</Reference>
<Target_Name>Bisphenol A, BPA</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>Binding assay</Affinity_Measurement_Method>
<Affinity_Measurement_Description>The binding specificity and relative affinity of the selected peptides to BPA were compared by assessing the number of BPA bound phages with varying peptide sequences displayed. Wild type M13 phage was used as a control. The number of wild type phages bound to BPA was 2.3 ± 0.2. NT denotes not tested.</Affinity_Measurement_Description>
<Brief_Description>Two rounds of negative panning followed the six rounds of positive screening procedure. The collected phages from the final round of positive panning were incubated in a microcentrifuge tube filled with Binding Buffer lacking BPA for 1 h and centrifuged as above in order to exclude phage particles with cross binding affinity to the tube surface.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2714</BiopanningDataSetID>
<Peptides>CSMSARQLC(20/25)</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:24960578</Reference>
<Target_Name>Beta-amyloid protein 42</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>Twenty-five Aβ42-binding clones with higher absorbance values were selected and amplified. Twenty clones showed the same peptide sequence: CSMSARQLC. His-tag-conjugated peptide CSMSARQLC bound to Aβ42 in a concentration-dependent manner. The peptide recognized Aβ13–35. In addition, molecular dynamics analysis and ELISA showed that the peptide predominately binds to I31 of Aβ42 by leucine and may also bind to F20 by alanine.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2715</BiopanningDataSetID>
<Peptides>DSRLEPNT
ASRAPSST
GGSVPTET
DRATSSNA</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:24977927</Reference>
<Target_Name>Envelope glycoprotein E2</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>f8-8mer phage display library (X8)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>Four phage clones specifically binding the E2 protein of CSFV were screened from f8/8 landscape phage library, and the phage E2P4 displaying octapeptide DRATSSNA significantly inhibited the CSFV infection in PK-15 cells at a higher titer.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2716</BiopanningDataSetID>
<Peptides>GVIMVIAVSCVF(11)[0.952 ± 0.244]
GSLVMLVFGYMG(4)[0.947 ± 0.239]</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:24979051</Reference>
<Target_Name>Sera IgG from patients with PMI</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>The original phage library as a negative control. The absorbance value at 450 nm was measured.</Affinity_Measurement_Description>
<Brief_Description>In the first round of affinity selection, microtiter wells were coated with purified sera IgG from patients without PMI to absorb nonspecific phages from the phage peptide library, and the unbounded phages were then incubated with sera IgG from patients with PMI to screen for phages containing potential peptide biomarkers. Another two rounds of affinity selection were carried out in the same way.</Brief_Description>
<BiopanningDataSet_Comments>Among the 17 positive phage clones, 11 had the same peptide sequence GVIMVIAVSCVF and four had the same peptide sequence GSLVMLVFGYMG.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2717</BiopanningDataSetID>
<Peptides>CSPLTENKC(7)
CTALNENKC(1)
CSQKSSLMC(1)
CSSSSVGTC(1)
CFPKKPNAC(1)
CPKSTQPQC(1)
CQYMDRSQC(1)
CNRAFVTDC(1)
CPHRGNEDC(1)</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:24689774</Reference>
<Target_Name>Anti-buffalo β-lactoglobulin antibody from rabbit 1</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>2718</BiopanningDataSetID>
<Peptides>CGALEENKC(1)
CSPYQENRC(1)
CPLNENKDC(1)
CPTNENREC(1)
CVAGQSPKC(1)
CTHAPLANC(1)
CNALSENKC(1)
CNPGSENKC(1)
CSPLLENRC(1)
CPFPRSAAC(1)
CPLHENKSC(1)
CGPQSENRC(1)
CPYSENRAC(1)
CSKTPPLTC(1)
CPFDENKSC(1)
CSALAENKC(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:24689774</Reference>
<Target_Name>Anti-buffalo β-lactoglobulin antibody from rabbit 2</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>2719</BiopanningDataSetID>
<Peptides>QAWTALT
SHLNSWL
YRAPWPP
QGSTTPN
TQWASYE
SVTTKLN
HTTSTTP
TPRFLNY
GSLYNLH
YLRPPSA
TVPGPSG
TLVGDIV
GMRWSEF
NPAIISI
VPPYWMS</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>15</Unique_Sequence_Number>
<Experimental_Method>Phage display (competitive panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:24819195</Reference>
<Target_Name>β2-glycoprotein I, β2GPI</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>Ultimately phage clones were obtained in elution step with polyclonal HAv anti-β2GPI antibody.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2720</BiopanningDataSetID>
<Peptides>ARLQLWL
QPWPTST
RADDLWL
FQASLLP
IAAHNPL
AALTHIW
AFSPLTI
SGVAPRL
RIGPELH</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>9</Unique_Sequence_Number>
<Experimental_Method>Phage display (competitive panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:24819195</Reference>
<Target_Name>β2-glycoprotein I, β2GPI</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>Ultimately phage clones were obtained in elution step with monoclonal chimeric IgG anti-β2GPI antibody (HCAL).</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2721</BiopanningDataSetID>
<Peptides>HYYPWLP
SHATGPW
TTAPLLP
MTTPSLH
FVLPANY
GLLASRS
VSLAGIA
FMMPHHQ
VRHINIF
WSRPATL
LSWMPVV
VNSSNYS</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>12</Unique_Sequence_Number>
<Experimental_Method>Phage display (competitive panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:24819195</Reference>
<Target_Name>β2-glycoprotein I, β2GPI</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>Ultimately phage clones were obtained in elution step with polyclonal LAv anti-β2GPI antibody.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2722</BiopanningDataSetID>
<Peptides>SAYHPWP
MGTQLSW
QLSTSAH
IPKTPYS
NPKIVLT
LSKYPSA
VTSYPFF
TGSFPAL</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:24819195</Reference>
<Target_Name>β2-glycoprotein I, β2GPI</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>2723</BiopanningDataSetID>
<Peptides>CKYMSVWKC
CHSMSSHQC</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>2</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:24819195</Reference>
<Target_Name>β2-glycoprotein I, β2GPI</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>2724</BiopanningDataSetID>
<Peptides>SLDSDRS(3/50)</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:24819195</Reference>
<Target_Name>Monoclonal chimeric IgG anti-β2GPI antibody, HCAL</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>Fifty phage clones were randomly picked. Three phage clones exhibited significantly higher binding to HCAL than to background in preliminary ELISA and were identical in their primary structure.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2725</BiopanningDataSetID>
<Peptides>KMDGNHP(1/20)</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:24819195</Reference>
<Target_Name>Low avidity (LAv) IgG anti-β2GPI polyclonal antibody from patient B</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>From each selection experiment, 20 phage clones were randomly picked and tested for their affinity towards corresponding polyclonal anti-b2GPI. Only one phage clone with displayed peptide KMDGNHP significantly and selectively bound to polyclonal LAv anti-β2GPI fraction.</BiopanningDataSet_Comments>
</Item></BiopanningDataSet></result>