<result><BiopanningDataSet><Item><BiopanningDataSetID>376</BiopanningDataSetID>
<Peptides>CSNRDARRC
CANKDVRRC
CANLDTRRC
CPNQDSRRC
CPNGDERNC
CVNNDGRLC</Peptides>
<Motif>C-x-N-x-D-x-R(2)-C</Motif>
<Unique_Sequence_Number>6</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>2-4</Rounds_of_Panning>
<Reference>PMID:17259343</Reference>
<Target_Name>HT-1376 human bladder tumor cell line</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>CX7C T7 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>The tumor cells were isolated from tumor xenografts in nude mice prepared using the HT-1376 human bladder tumor cell line. Phage that bound to normal bladder cells isolated from mouse bladder tissues, normal rat kidney cells, or human umbilical vascular endothelial cells were subtracted during the biopanning procedure.</Brief_Description>
<BiopanningDataSet_Comments>After the second round of screening, the numbers of phage were enriched approximately by 1,000-fold and did not increase in further steps. Ninety-six phage clones were picked from the enriched phage library after the second and third rounds of screening. Twenty of the 96 clones showed selective binding to HT-1376 cells. These clones were sequenced. Six sequences were given in the published paper. It has been shown that CSNRDARRC selectively targeted and bound to primary bladder tumor tissues and can be used to detect tumor cells in urine.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>377</BiopanningDataSetID>
<Peptides>AFNMFDFGV
VTKSLRVFG
SESHRVKSA
QLGPPV</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>4</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>1-2</Rounds_of_Panning>
<Reference>PMID:17129616</Reference>
<Target_Name>Anti-HAV polyclonal antibody IgG</Target_Name>
<Template_Name>Hepatitis A virus, HAV</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>J404 phage display library (X9)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Mouse anti-human IgG coupled magnetic microbeads were blocked overnight at 4 ◦C in PBS/0.1% BSA (w/v). These beads were then incubated overnight at 4 ◦C with anti-HAV serum and washed four times with PBS/0.1% BSA (w/v)/0.1% Tween 20 (v/v) (PBSB-T). The beads were further blocked with excess of UV-killed wild-type phage M13K07 particles for 4 h at 4 ◦C and then used to screen the library.</Brief_Description>
<BiopanningDataSet_Comments>Since there was no enrichment after a second round of affinity selection, the 75 selected clones from the first round of panning, were tested. After a series of immunoscreenings, 4 clones are found to be disease-specific. Among them, VTKSLRVFG was recognised by 92% of the positive sera. Three of the four cloned peptides showed similarity in their amino acid sequences with at least one of the VP3 and VP1 antigenic proteins of HAV.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>378</BiopanningDataSetID>
<Peptides>SVSVGMKPSPRP(25)
WPLHTSVYPPSP(11)
NTLPPFSPPSPP(5)
SFPDSNIAPSSP(3)
QHAPSNSKSVLT(2)
WPTYLNPSSLKA(1)
GPSGNLHIRPAS(1)
SPLLSTRAVQLS(1)
SPMFTMIQGDAQ(1)
VNSHQALWSPAQ(1)
STLPPPLRFANV(1)
SFNQPYLYKTAF(1)
YHTRIALPDNLP(1)
AQSTAFQKPLLM(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>14</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:18006841</Reference>
<Target_Name>Non-small cell lung cancer (CL1-5)</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>CL1-5 cells (lung cancer cell line) were injected s.c. into SCID mice to produce lung cancer xenografts.</Brief_Description>
<BiopanningDataSet_Comments>The paper suggested that PSP motif was crucial for peptide binding to the tumor neovasculature. The most frequent peptide SVSVGMKPSPRP was shown to be a good candidate for targeted drug delivery to solid tumors.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>379</BiopanningDataSetID>
<Peptides>PPWDFDAGEGIH(1)
DYAWDDFYAMGD(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:17371999</Reference>
<Target_Name>Seam 3 monoclonal antibody</Target_Name>
<Template_Name>Neisseria meningitidis serogroup B capsular polysaccharide (MenB CP)</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>X9 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>380</BiopanningDataSetID>
<Peptides>DYAWDQTHQ(3)
DAGEGGPRV(2)
DAGDSGYLT(1)
DAGDHSHPQ(1)
DAGEVYPGP(1)
DAGDSAYSQ(1)
DAGDHRAAA(1)
EFDAGDVLL(1)</Peptides>
<Motif>D-A-G-[ED]</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:17371999</Reference>
<Target_Name>Seam 3 monoclonal antibody</Target_Name>
<Template_Name>Neisseria meningitidis serogroup B capsular polysaccharide (MenB CP)</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>X12 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>DYAWDQTHQ has been shown to be a promising lead candidate for the development of an effective and affordable anti-MenB vaccine.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>381</BiopanningDataSetID>
<Peptides>ISYEHPLLTGLLLEQRHVD
LDGDVSKLHPLLVNFLKGD
VESSHPLLVGLLGKQQATV
SEGLHPLLTALLAPQVTQW
ALHDQQSLHPLLAEALLRD
PMVQHPWLVGLLVSAEGVS
DLAEPVKLHPLLSMYLSNL
VAQMHPGLSELLLASHFHQ
VHVTMPFLTSLLTGQPTSV
MPLHSPYLLSLLTGSGQSL
VDLEYPMLVHLLQYGRELS
PVETHPRLLKLLTRAEYPM
TEVTHPLLASLLQYGVQVS
ATTPPTQLHPLLTQFLRTD
SSLEHPWLTMLLGKPHNMW
PVTAYPMLAELLLPTGQLR
MSQSVSDLHPLLGLLLTAD
VATNHPWLTMLLNGQASGE
PLALHPLLASLLDPGRQLV
TQMEYPLLTQLLGGRTMEE
LLEAHPLLTGLLGASSLEL
ILEEHPLLASLLTETSRGM
LSQEYPWLTRLLDSGQLGS
TWLEYPLLTDLLLPSWRQD
SAADHPSLLRLLTGDFPYE
ISYEHPLLTGLLLDSVMW
LELEATSLHPLLLQLIKQV
PVFEHPRLVGLLVGTDIAS
LGESHPLLMQLLTENVGTH
VEENPLLLEMLLSASKASS
MVAQNPLLGGLLLGSMDTM
PTSSPLLLDLLLGRPVETV
PFYTHPMLSSLLLGPPSMT
PTVEHPMLSSLLRGAANEF
TVVQHPWLTGLLIGSGQDA
SLEAHPLLSALLQDQMGGD
PLSDHPMLLELLNHNSMRN
HQEHPLLLHMLLGGSQEVE
NHETHPLLSKLLLSPLEQT
MSDHPLLLSYLLETTAVLP
GVLDHPLLFQLLSSETRVL
IAGEHPMLWGLLRAGGLPE
PADNMPLLRTLLLGSGIEV
TIDSHPMLHSLLSQRGLVA
VAHTHPLLVGLLKGSITGP
ALSDSPLLLSLLLGHPDWQ
TYVDHPLLAELLLGEVGMN
ADGSPMELHPLLSRLITAP
PVEGHPWLLGLLVGAEVDV
ALSSPSDLNPLLTSLLSQS
MTLEHPGLTALLASQSLMG
SVDQHPMLMDLLTGLKRAE
MVEHPRLLSLLLDRSDVPM</Peptides>
<Motif>H-P-L(2)-x(2)-L(2)</Motif>
<Unique_Sequence_Number>53</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:17595321</Reference>
<Target_Name>Peroxisome proliferator-activated receptor gamma, PPAR-gamma</Target_Name>
<Template_Name>PPAR-gamma coactivators</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>X7-LXXLL-X7 M13 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>PPAR-gamma was expressed in Sf9 insect cells and biotinylated.
</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>382</BiopanningDataSetID>
<Peptides>SLLHPLLVDLLQMGGAS
SSVLNPLLAELLASGSS
SYLLDLLLGTSDVTTNV</Peptides>
<Motif>L-x(2)-L(2)</Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:17595321</Reference>
<Target_Name>Peroxisome proliferator-activated receptor gamma, PPAR-gamma</Target_Name>
<Template_Name>PPAR-gamma coactivators</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>SS-X16-S M13 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>PPAR-gamma was expressed in Sf9 insect cells and biotinylated.</Brief_Description>
<BiopanningDataSet_Comments>Of the 130 peptides sequenced, 53 exhibited unique sequences.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>383</BiopanningDataSetID>
<Peptides>AVGLSPDGSRGV(10)
GGSGDSRPPILG(1)
TDTRPAHTGDAQ(1)
PHIQADTRPHA(1)
PDRPVPSLPITW(1)
TPDSRGIHGAPS(1)
PDGRPSPGHLPA(1)
LLADTTHHRPWT(1)</Peptides>
<Motif>P-D-[TSG]-R-P</Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4-5</Rounds_of_Panning>
<Reference>PMID:17725384</Reference>
<Target_Name>Anti-MUC1 monoclonal antibody PR81</Target_Name>
<Template_Name>Mucin-1, MUC-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.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>The library was first screened against an irrelevant monoclonal anti-digoxin antibody that would not be expected to bind specifically to MUC1-specific epitopes. Additionally, in order to omit those phages that bind to BSA, the library was screened against BSA-coated wells.</Brief_Description>
<BiopanningDataSet_Comments>Fourty clones were randomly selected from each of the fourth and fifth rounds of biopanning. Among the 80 clones, 17 phage clones that showed higher binding activities (7 clones from the fourth round and 10 clones from the fifth round) were sequenced.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>384</BiopanningDataSetID>
<Peptides>GHLSDWVYVPMR(5)
VSMDDGWVFVQP(4)
SHKSDWIFLPNA(3)
AHKSDNWVFLPE(1)
THINEKWVFLPQ(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>5</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:17916189</Reference>
<Target_Name>Gamma-aminobutyric acid receptor-associated protein</Target_Name>
<Template_Name>Calreticulin</Template_Name>
<Structure_of_Target_Template_Complex>3DOW,</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>In fact, recombinant GST-GABARAP fusion protein was used for screening.</Brief_Description>
<BiopanningDataSet_Comments>Seventy randomly chosen true positive clones were sequenced. Only those with high occurrence and/or high affinity to GABARAP were given in the original paper. Calreticulin and GABARAP interact with a dissociation constant Kd=64 nm and a mean lifetime of the complex of 20 min. Thus, the interaction between GABARAP and calreticulin is the strongest so far reported for each protein.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>385</BiopanningDataSetID>
<Peptides>KSLSRHDIHHHH(4)</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:17214965</Reference>
<Target_Name>Anti-HGF-cMET monoclonal antibody SFN68</Target_Name>
<Template_Name>Hepatocyte growth factor-hepatocyte growth factor receptor complex (HGF-cMET)</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>Ph.D.-7, C7C and 12 libraries were used in panning. Of 14 clones with specific reactivity, four shared the amino acid sequence KSLSRHDHIHHH. This is the only mimotope given in the original paper.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>386</BiopanningDataSetID>
<Peptides>RVPPRYHAKISPMVN(20)</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:17005302</Reference>
<Target_Name>Anti-GMDP monoclonal antibody E6/1.2</Target_Name>
<Template_Name>N-acetylglucosaminyl-beta1-4-N-acetylmuramyl-alanyl-d-isoglutamine (GMDP)</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>f3-15mer phage display library (X15)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>Twenty clones were selected and sequenced. All of them has the identical sequence RVPPRYHAKISPMVN.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>387</BiopanningDataSetID>
<Peptides>YQDSAKT(17)
NDRGLLA(5)
VSVGMLW(4)
QDTGLLA(2)
SNPGWLI(2)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>5</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:17761669</Reference>
<Target_Name>Beta amyloid peptide (12-28)</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>Only peptides found in two or more clones are shown.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>388</BiopanningDataSetID>
<Peptides>SVLDRQR(15)
SARTFLP(3)
VDANKFL(2)
SHREPLQ(2)</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:17761669</Reference>
<Target_Name>Beta amyloid peptide (25-35)</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>Only peptides found in two or more clones are shown. SVLDRQR was found to be effective blocker of the toxic effect of β-amyloid on cultured neuronal cells.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>389</BiopanningDataSetID>
<Peptides>LGSYKPS(7)
IQLHPRL(4)
YGAAKSG(3)
QATGLLA(3)
SFHPPSM(2)
QDTGLLA(1)
EWGGAQF(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:17761669</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.-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>LGSYKPS was found to be effective blocker of the toxic effect of β-amyloid on cultured neuronal cells.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>390</BiopanningDataSetID>
<Peptides>NIPTPKP(3)
SARTFLP(2)
QATGLLA(2)
IQSPHFF(2)
SMPTYNK(2)
GTHVQAT(2)
VSVGMLW(2)
NDRGLLA(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:17761669</Reference>
<Target_Name>Beta amyloid peptide (1-20)</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>VSVGMLW was found to be effective blocker of the toxic effect of β-amyloid on cultured neuronal cells. </BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>391</BiopanningDataSetID>
<Peptides>CPYANHLLC(11)
CPYANPSMC(4)
CPYHNQFLC(2)
CPKSAHKHC(2)
CLYTNPALC(1)</Peptides>
<Motif>P-Y-x-N-x(2)-L</Motif>
<Unique_Sequence_Number>5</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:18025245</Reference>
<Target_Name>Anti-PYANPSL polyclonal antibody IgG</Target_Name>
<Template_Name>Peptide PYANPSL</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>392</BiopanningDataSetID>
<Peptides>CWAANPSMC(6)
CRALNPSMC(5)
CPINPSMAC(4)
CPFNPSMAC(3)
CLNPSSSQC(2)
CPYNPSAHC(1)
CYNPSSSWC(1)</Peptides>
<Motif>NPSM</Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:18025245</Reference>
<Target_Name>Anti-WAANPSM polyclonal antibody  IgG</Target_Name>
<Template_Name>Peptide WAANPSM</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>393</BiopanningDataSetID>
<Peptides>NPGTCKDKWIECLLNG(9)
LKNYCRKCSNRCTPTG(4)
NLIWCRKEFARCTSDM(3)</Peptides>
<Motif></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:17803452</Reference>
<Target_Name>Tumor-associated glycoprotein (TAG-72)</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>f88-Cys6 phage display library (X4CX6CX4)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>Twenty-three clones were selected for sequencing. However, only above squences were given in the original paper. NPGTCKDKWIECLLNG showed evidence of significant specific binding when presented as the radiolabeled phage to tumor in vivo and especially in vitro with cells and solid tumor.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>394</BiopanningDataSetID>
<Peptides>EDIKPKTSLAFR(6)
TQPADLQTHNHN(1)
FDHSSKWTRTSP(1)
YSHNTITNLYFS(1)
WPRYAESTLQLR(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>5</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:17687498</Reference>
<Target_Name>Nasopharyngeal carcinoma cell CEN-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.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>After the fifth round, all sequenced clones have the same sequence EDIKPKTSLAFR, which might be a candidate as diagnostics and therapeutics for nasopharyngeal carcinoma.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>395</BiopanningDataSetID>
<Peptides>SVSVGMKPSPRP(2)
IHPPTPPLTMLR(1)
HLWPVNVASAQS(1)
GSSRAQMTSHRP(1)
SVGSSPHPGRHT(1)
SDSPHGAVPPLA(1)
HWTPWQHVSSFW(1)
HPPDNARRIGCR(1)
WSKNNKSPQLSP(1)
GSMCPYVRWYTP(1)
LNAAYSATFMAR(1)</Peptides>
<Motif>S-V-S-x(2)-M-x-P-S-P-R-P</Motif>
<Unique_Sequence_Number>11</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>6</Rounds_of_Panning>
<Reference>PMID:18053412</Reference>
<Target_Name>l,2-Dioleoyl-sn-glycero-3-phosphatidylserine</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>Ligands that bind to PS can be used for noninvasive imaging of therapy-induced cell death, particularly apoptosis.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>396</BiopanningDataSetID>
<Peptides>CFHNHNPLC(20)
CTVNTQSKC(10)
CNHMPHPLC(5)
CVGQKQESC(5)
CLKAFHKEC(3)
CHNQPQATC(3)
CGPTPTKTC(2)
CPLFSSKTC(2)
CLTKSYTSC(2)
CVTQHRGDC(2)
CAPNSHWTC(1)
CRLDHALQC(1)
CILNNTPWC(1)
CKDANSPHC(1)
CPTRAALTC(1)
CQKHNTRFC(1)
CMPHTHRIC(1)
CSQSHPRHC(1)
CTQPRSTGC(1)
CFPNTRATC(1)
CSPVHQQSC(1)
CPKSDHKFC(1)
CAPKQTQHC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>23</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>1</Rounds_of_Panning>
<Reference>PMID:17324139</Reference>
<Target_Name>Mouse inflammatory small bowel</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>SQSHPRH has a specific high affinity for inflammatory bowel.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>397</BiopanningDataSetID>
<Peptides>HPAIVHISPQWA(1)
ISPAPHLLTSRF(1)
HHVDSLPTLDWK(1)
MPTSSTAPPPLI(1)
QMVYGPLRSTEQ(1)
HGTNQALSLLTP(1)
KLPHQPPSAAVH(1)
ANYFSSPIKHAT(1)
NSLTSEPLRYGG(1)
VLNPQTTVMPPL(1)
SPWTSFLQWARG(1)
HPPHNMHLPAFS(1)
APFAHSGPLAFS(1)
ATTSLTPTMANH(1)
QFPPKLTNNSML(1)
MPTLTRAPHTAC(1)
TPLHPKSLMVWH(1)
QATGPTTPTTSG(1)
YTDNSLGTSVGK(1)
LPRKTPDYLQTR(1)
SNSMHLMTMTGL(1)
TPSLEQRTVYAK(1)
TSLRELPAEWSR(1)
SVPPRYTLTLQW(1)
LYSASTPPDPGG(1)
SHGKPPSRSPWT(1)
TLDWTKPPLRSG(1)
FPMSSYKTYATP(1)
YNLGQLEAQITS(1)
ASQGYPEHRHAS(1)
INTPANRNPVLG(1)
ITLSATKGAAPS(1)
HKSYLPVPSLYG(1)
WDTNRNAASTPG(1)
SPPPSNAGSHHV(1)
QTTKLHIMDTGF(1)
SYQTLKQHLPYG(1)
THPPNPSVSIGG(1)</Peptides>
<Motif>S-P-T-P-S-[PL]-P(2)-S-A-G(2)</Motif>
<Unique_Sequence_Number>38</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:17657770</Reference>
<Target_Name>Human blood outgrowth endothelial cells, HBOEC</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>Before HBOEC screening, human umbilical vein endothelial cells (HUVEC) were used to remove non-specific binding phages.</Brief_Description>
<BiopanningDataSet_Comments>Fourty clones were sequenced. 38 different peptide sequences were deduced and 2 phage clones contained no inserts.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>398</BiopanningDataSetID>
<Peptides>AMSFYNTPDAKE(1)
TLCNNSMSPGCK(1)
IEHTRYNSRTAY(1)
QATKYHSANRHP(1)
NYLHNHPYGTVG(1)
GQSPHSYQPRTY(1)
NNALLNRQLHFS(1)
HQVPSHNNSLGP(1)</Peptides>
<Motif></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:16958043</Reference>
<Target_Name>Beta-nerve growth factor, Beta-NGF</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>These peptide sequences were obtained when the pH of elution buffer was at 6.0.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>399</BiopanningDataSetID>
<Peptides>RSTSPDPLNYVR(1)
ALRTPLSHAPTK(1)
NMTAVTKLPAPW(1)
QMHPSIALPLWY(1)
QMHPSIALPHWY(1)
LDLALGQRPPRH(1)
DARHLPPVTLST(1)
SVSVGMKPSPRP(1)</Peptides>
<Motif></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:16958043</Reference>
<Target_Name>Beta-nerve growth factor, Beta-NGF</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>These peptide sequences were obtained when the pH of elution buffer was at 4.5.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>400</BiopanningDataSetID>
<Peptides>SVSVGMKPSPRP(2)
DSAVDYTGWLRR(1)
SVWYYXIHYDMX(1)
SLTGAALGPSGW(1)
VPHSKYPRGINA(1)
QFSLPVAKLVNR(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>6</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:16958043</Reference>
<Target_Name>Beta-nerve growth factor, Beta-NGF</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>These peptide sequences were obtained when the pH of elution buffer was at 2.8.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item></BiopanningDataSet></result>