Effects of heme addition on formation of stable human globin chains and hemoglobin subunit assembly in a cell-free system

被引:13
作者
Adachi, K [1 ]
Zhao, Y
Surrey, S
机构
[1] Childrens Hosp Philadelphia, Div Hematol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[3] Thomas Jefferson Univ, Jefferson Med Coll, Dept Med, Cardeza Fdn Hematol Res, Philadelphia, PA 19107 USA
关键词
heme; hemoglobin; hemoglobin subunits; cell-free system; cotranslation; nascent protein;
D O I
10.1016/S0003-9861(03)00089-4
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
Our previous assembly studies to form hemoglobin hetero-dimers and -tetramers using a coupled transcription/translation cell-free system suggested that alpha-globin chains bind to nascent non-alpha chains during and/or soon after translation to promote hemoglobin formation [Adachi et al., J. Biol Chem. 2002 (277) 13415]. In this report effects of CN-hemin on subunit assembly were studied using this cell-free system. Addition of CN-hemin and excess unlabeled heme-containing partner chains during synthesis leads to formation of radiolabeled heme-containing alpha(h)beta(h) hetero-dimers. In contrast, in the absence of added CN-hemin, unlabeled heme-containing alpha or beta chains can assemble with newly synthesized radiolabeled beta- and alpha-globin chains to form heme-containing alpha(h)beta(h) and semi-alpha (alpha(h)beta(0)) or semi-beta (alpha(0)beta(h)) hetero-dimers, respectively. These results suggest the existence of semi-hemoglobins as intermediates prior to formation of heme-containing alpha(h)beta(h) and indicate transfer of heme from alpha and/or beta chains into semi-hemoglobin heterodimers to form heme-containing hetero-dimers. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:99 / 106
页数:8
相关论文
共 19 条
[1]   Assembly of γ- with α-globin chains to form human fetal hemoglobin in vitro and in vivo [J].
Adachi, K ;
Zhao, Y ;
Yamaguchi, T ;
Surrey, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (17) :12424-12429
[2]   Assembly of human hemoglobin (Hb) β- and γ-globin chains expressed in a cell-free system with α-globin chains to form Hb A and Hb F [J].
Adachi, K ;
Zhao, Y ;
Surrey, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (16) :13415-13420
[3]  
BENESCH RE, 1990, J BIOL CHEM, V265, P14881
[4]  
Benz E J Jr, 1975, Prog Hematol, V9, P107
[5]  
BUNN HF, 1968, J BIOL CHEM, V243, P465
[6]  
BUNN HF, 1986, HEMOGLOBIN MOL GENET, P168
[7]   Biophysical characterization of the α-globin binding protein α-hemoglobin stabilizing protein [J].
Gell, D ;
Kong, Y ;
Eaton, SA ;
Weiss, MJ ;
Mackay, JP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (43) :40602-40609
[8]  
GIBSON QH, 1963, J BIOL CHEM, V238, P1384
[9]   Properties of human hemoglobins with increased polarity in the α- or β-heme pocket -: Carbonmonoxy derivatives [J].
Karavitis, M ;
Fronticelli, C ;
Brinigar, WS ;
Vasquez, GB ;
Militello, V ;
Leone, M ;
Cupane, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (37) :23740-23749
[10]   An abundant erythroid protein that stabilizes free α-haemoglobin [J].
Kihm, AJ ;
Kong, Y ;
Hong, W ;
Russell, JE ;
Rouda, S ;
Adachi, K ;
Simon, MC ;
Blobel, GA ;
Weiss, MJ .
NATURE, 2002, 417 (6890) :758-763