                         SEQUENCE LISTING

<110>  Hong Kong Baptist University
       WONG, Ka Leung
 
<120>  MULTI-MODAL BIOPROBE FOR BLADDER CANCER IMAGING AND PHOTODYNAMIC 
       THERAPY

<130>  P8084US03

<140>  15/352,561
<141>  2016-11-15

<160>  5     

<170>  PatentIn version 3.5

<210>  1
<211>  10
<212>  PRT
<213>  Artificial Sequence

<220>
<223>  Peptide sequence incorporating non-naturally occuring amino acids
       synthesized in the lab


<220>
<221>  MISC_FEATURE
<222>  (1)..(1)
<223>  Xaa in position one is 6-aminocaproic acid

<220>
<221>  DISULFID
<222>  (2)..(10)
<223>  The side chain of C in position two taken together with the side 
       chain of C in position ten form a disulfide bond

<220>
<221>  MISC_FEATURE
<222>  (2)..(2)
<223>  C in position two is a D-amino acid

<220>
<221>  MISC_FEATURE
<222>  (10)..(10)
<223>  C in position ten is a D-amino acid

<400>  1

Xaa Cys Gly Asp Gly Arg Met Gly Phe Cys 
1               5                   10  


<210>  2
<211>  10
<212>  PRT
<213>  Artificial Sequence

<220>
<223>  Peptide sequence incorporating non-naturally occuring amino acids
       synthesized in the lab


<220>
<221>  MISC_FEATURE
<222>  (1)..(1)
<223>  Xaa in position one is 6-aminocaproic acid

<220>
<221>  MISC_FEATURE
<222>  (2)..(2)
<223>  C in position two is a D-amino acid

<220>
<221>  DISULFID
<222>  (2)..(10)
<223>  The side chain of C in position two taken together with the side 
       chain of C in position ten form a disulfide bond

<220>
<221>  MISC_FEATURE
<222>  (10)..(10)
<223>  C in position ten is a D-amino acid

<400>  2

Xaa Cys Gly Arg Leu Lys Glu Lys Lys Cys 
1               5                   10  


<210>  3
<211>  15
<212>  PRT
<213>  Artificial Sequence

<220>
<223>  Peptide sequence incorporating non-naturally occuring amino acids
       synthesized in the lab


<220>
<221>  MISC_FEATURE
<222>  (1)..(1)
<223>  Xaa in position one is 6-aminocaproic acid

<220>
<221>  MISC_FEATURE
<222>  (4)..(4)
<223>  R in position four is a D-amino acid

<220>
<221>  MISC_FEATURE
<222>  (6)..(6)
<223>  Xaa in position six is 6-aminocaproic acid

<220>
<221>  MISC_FEATURE
<222>  (7)..(7)
<223>  C in position seven is a D-amino acid

<220>
<221>  DISULFID
<222>  (7)..(15)
<223>  The side chain of C in position seven taken together with the 
       side chain of C in position fifteen form a disulfide bond

<220>
<221>  MISC_FEATURE
<222>  (15)..(15)
<223>  C in position fifteen is a D-amino acid

<400>  3

Xaa Arg Arg Arg Lys Xaa Cys Gly Arg Leu Lys Glu Lys Lys Cys 
1               5                   10                  15  


<210>  4
<211>  4
<212>  PRT
<213>  Artificial Sequence

<220>
<223>  Peptide sequence incorporating non-naturally occuring amino acids
       synthesized in the lab


<220>
<221>  MISC_FEATURE
<223>  The R is the second position is a D-amino acid

<220>
<221>  MISC_FEATURE
<223>  The R in the second position is a D-amino acid

<400>  4

Arg Arg Arg Lys 
1               


<210>  5
<211>  9
<212>  PRT
<213>  Artificial Sequence

<220>
<223>  Peptide sequence incorporating non-naturally occuring amino acids
       synthesized in the lab


<220>
<221>  MISC_FEATURE
<222>  (1)..(1)
<223>  C in position one is a D-amino acid

<220>
<221>  DISULFID
<222>  (1)..(9)
<223>  The side chain of C in position one taken together with the side 
       chain of C in position nine form a disulfide bond

<220>
<221>  MISC_FEATURE
<222>  (9)..(9)
<223>  C in position nine is a D-amino acid

<400>  5

Cys Gly Arg Leu Lys Glu Lys Lys Cys 
1               5                   


