Analysis of activation-induced conformational changes in p47(phox) using tryptophan fluorescence spectroscopy

被引:86
作者
Swain, SD
Helgerson, SL
Davis, AR
Nelson, LK
Quinn, MT
机构
[1] MONTANA STATE UNIV,DEPT VET MOL BIOL,BOZEMAN,MT 59717
[2] MONTANA STATE UNIV,DEPT MICROBIOL,BOZEMAN,MT 59717
[3] BAXTER HEALTHCARE CORP,DUARTE,CA 91010
关键词
D O I
10.1074/jbc.272.47.29502
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
Activation of the neutrophil NADPH oxidase requires translocation of cytosolic proteins p47(phox), P67(phox), and Pac to the plasma membrane or phagosomal membrane, where they assemble with membrane-bound flavocytochrome b, During this process, it appears that p47(phox) undergoes conformational changes, resulting in the ex exposure of binding sites involved in assembly and activation of the oxidase, In the present study, we have directly evaluated activation-induced conformational changes in p47(phox) using tryptophan fluorescence and circular dichroism spectroscopy. Treatment of p47(phox) with amphiphilic agents known to activate the NADPH oxidase (SDS and arachidonic acid) caused a dose dependent quenching in the intrinsic tryptophan fluorescence of p47(phox), whereas treatment with a number of other amphiphilic agents that failed to activate the oxidase had no effect on p47(phox) fluorescence. In addition, the concentration range of activating agents required to induce changes in fluorescence correlated with the concentration range of these agents that induced maximal NADPH oxidase activity in a cell-free assay system. We next determined if activation by phosphorylation caused the same type of conformational changes in p47(phox). Protein kinase C phosphorylation of p47(phox) in vitro resulted in comparable quenching of fluorescence, which also correlated directly with NADPH oxidase activity, Finally, the circular dichroism (CD) spectrum of p47(phox) was significantly changed by the addition of SDS, whereas treatment with a non-activating detergent had no effect on the CD spectrum, These results support the conclusion that activation by amphiphilic agents results in changes in the secondary structure of p47(phox). Thus, our studies provide direct evidence linking conformational changes in p47(phox) to the NADPH oxidase activation/assembly process and also further support the hypothesis that amphiphile-mediated activation of the NADPH oxidase induces changes in p47(phox) that are similar to those mediated by phosphorylation in rico.
引用
收藏
页码:29502 / 29510
页数:9
相关论文
共 61 条
[1]  
BOXER GJ, 1985, HOSP PRACT, V40, P69
[2]  
BROMBERG Y, 1985, J BIOL CHEM, V260, P3539
[3]  
CHANOCK SJ, 1994, J BIOL CHEM, V269, P24519
[4]   FLUORIMETRIC DETERMINATION OF CRITICAL MICELLE CONCENTRATION AVOIDING INTERFERENCE FROM DETERGENT CHARGE [J].
CHATTOPADHYAY, A ;
LONDON, E .
ANALYTICAL BIOCHEMISTRY, 1984, 139 (02) :408-412
[5]  
CLARK RA, 1987, J BIOL CHEM, V262, P4065
[6]   MOLECULAR EVENTS IN THE ACTIVATION OF HUMAN NEUTROPHILS FOR MICROBIAL KILLING [J].
COHEN, MS .
CLINICAL INFECTIOUS DISEASES, 1994, 18 :S170-S179
[7]  
COREY SJ, 1991, J LAB CLIN MED, V118, P343
[8]   ACTIVATION OF THE HUMAN NEUTROPHIL NICOTINAMIDE ADENINE-DINUCLEOTIDE PHOSPHATE (NADPH)-OXIDASE BY PROTEIN KINASE-C [J].
COX, JA ;
JENG, AY ;
SHARKEY, NA ;
BLUMBERG, PM ;
TAUBER, AI .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (05) :1932-1938
[10]   A DOMAIN OF P47(PHOX) THAT INTERACTS WITH HUMAN NEUTROPHIL FLAVOCYTOCHROME B(558) [J].
DELEO, FR ;
NAUSEEF, WM ;
JESAITIS, AJ ;
BURRITT, JB ;
CLARK, RA ;
QUINN, MT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (44) :26246-26251