INVOLVEMENT OF THYMOSIN-BETA-4 AND ENDOPROTEINASE ASP-N IN THE BIOSYNTHESIS OF THE TETRAPEPTIDE ACSERASPLYSPRO A REGULATOR OF THE HEMATOPOIETIC SYSTEM

被引:106
作者
GRILLON, C
RIEGER, K
BAKALA, J
SCHOTT, D
MORGAT, JL
HANNAPPEL, E
VOELTER, W
LENFANT, M
机构
[1] CNRS,INST CHIM SUBST NAT,AVE TERRASSE,F-91198 GIF SUR YVETTE,FRANCE
[2] CENS,SERV BIOCHIM,INGN PROT LAB,F-91191 GIF SUR YVETTE,FRANCE
[3] UNIV ERLANGEN NURNBERG,INST PHYSIOL CHEM,W-8520 ERLANGEN,GERMANY
[4] UNIV TUBINGEN,INST PHYSIOL,PHYS BIOCHEM ABT,W-7400 TUBINGEN 1,GERMANY
[5] UNIV TUBINGEN,INST CHEM,PHYS BIOCHEM ABT,W-7400 TUBINGEN 1,GERMANY
关键词
AcSDKP peptide: Hematopoietic regulator; Bone marrow cell; Endoproteinase Asp-N; Thymosin β[!sub]4[!/sub]. Enzymatic maturation;
D O I
10.1016/0014-5793(90)81322-F
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is shown that AcSDKP a new regulator of the hematopoietic system can he generated from thymosin β4 by a one-step enzymatic cleavage in vitro and in vivo. AcSDKP and Tβ4 were both detected in bone marrow cells (BMC'). Incubation of [3H]Tβ4 with either intact or lysed BMC led to the formation of [3H]AcSDKP whereas the labelled tetrapeptide was not degraded under these conditions. Model enzymatic degradation of Tβ4 carried out with bacterial enzymes suggests that a mammalian endoproteinase Asp-N might be involved in the formation of AcSDKP through the specific cleavage of the 4Pro-5 Asp peptide bond of T β4. © 1990.
引用
收藏
页码:30 / 34
页数:5
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