Title : Novel glycosylated forms of human plasma
endostatin and circulating
endostatin-related
fragments of collagen XV
Abstract :
- Circulating elongated forms of the angiogenesis inhibitor and potential anti-cancer drug endostatin were isolated from human blood filtrate
- Immunoreactive endostatin was identified by a polyclonal rabbit antiserum raised against an N-terminal epitope of the polypeptide and purified by consecutive chromatographic steps and immunoblotting
- N- and C-terminal sequence analyses of the isolated molecules revealed different forms of endostatin starting with V(117) HLRPAR
- lacking the last and final three residues of the noncollagenous domain 1 (NC-1) of collagen XVIII , respectively
- These polypetides are found to be O-glycosylated at T(125) ( residue 9 ) with a glycan structure of the mucin type consisting of galactose N-acetylgalactosamine and N-acetylneuraminic acid residues
- Carbohydrate analyses were performed via the semiquantitative HPLC-electrospray ionization mass spectrometry (ESMS) technique after exoglycosidase hydrolysis
- Circulating endostatins are present as sialoglycoprotein (22 000 and 21 841 Da +/- 0.02%) and asialoglycoprotein structures (21 710 and 21 549 Da +/- 0.02%), while the two completely deglycosylated forms are obtained only after enzymatic incubation
- The described glycosylated endostatins may represent intermediates in the proteolytic pathway of the NC-1 domain of collagen XVIII resulting in bioactive endostatins
- Furthermore, immunoreactive endostatin-related C-terminal fragments of human collagen XV are found in the hemofiltrate
- These polypeptides exhibit the N-terminal sequences P(66) HLLPPP
- and Y(81) EKPALH
- of the collagen XV NC-1 domain
- ESMS and immunoblotting analyses reveal three glycosylated polypeptides with a molecular mass ranging from 16 to 21 kDa
- Due to the high degree of homology between collagen XV and collagen XVIII as well as their analoqous proteolytic processing, functional similarities of collagen XVIII- and XV-related fragments should be revealed in future experiments
Output (sent_index, trigger,
protein,
sugar,
site):
- 0. glycosylated, , endostatin, -, -
- 13. glycosylated, , -, -, polypeptides
- 5. O-glycosylated, , -, -, T(125)
- 5. O-glycosylated, , -, -, residue 9
- 5. galactose, , -, -, residues
- 7. asialoglycoprotein, , asialoglycoprotein, -, -
- 7. sialoglycoprotein, , sialoglycoprotein, -, -
Output(Part-Of) (sent_index,
protein,
site):
- 0. endostatin, fragments
- 14. XV-related, fragments
- 14. collagen XVIII, fragments
- 4. collagen XVIII, domain
- 8. collagen XVIII, domain
- 9. endostatin, fragments
*Output_Site_Fusion* (sent_index,
protein,
sugar,
site):