메뉴 건너뛰기




Volumn 8, Issue 6, 2010, Pages 1351-1360

Exploring neoglycoprotein assembly through native chemical ligation using neoglycopeptide thioesters prepared via N→S acyl transfer

Author keywords

[No Author keywords available]

Indexed keywords

ACYL TRANSFER; CLICK CHEMISTRY; NATIVE CHEMICAL LIGATION; PROTEIN FRAGMENTS; THIOESTERS;

EID: 77749286506     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b920535g     Document Type: Article
Times cited : (34)

References (63)
  • 49
    • 77749253827 scopus 로고    scopus 로고
    • See supporting information for further details
    • See supporting information for further details.
  • 50
    • 77749297238 scopus 로고    scopus 로고
    • Note
    • Note that 7 (Fig. 1) is not a thioester though conversion is plotted on the same graph for comparison.
  • 54
    • 77749253825 scopus 로고    scopus 로고
    • Note
    • Coupling of cysteine to hydroxy-functionalised resins employing HBTU/HOBt may well lead to racemisation of the C-terminal cysteine though this should be of little consequence since the cysteine is excised. Cysteine racemisation can also be minimised by using a trityl resin, e.g. NovaSYN TGT
  • 56
    • 77749278716 scopus 로고    scopus 로고
    • Note
    • The D8E mutation is non-essential as hydrolysis at Asp is slow relative to thioesterification but the conservative mutation is unlikely to affect bioactivity as this region does not bind the EPO receptor.
  • 61
    • 77749253824 scopus 로고    scopus 로고
    • D. Macmillan, J. Blanc, J. PCT, Int. Appl., 2008, WO2008001109
    • (2008)
    • MacMillan, D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.