Monitoring of recombinant survival motor neuron protein using fiber-optic surface plasmon resonance

被引:23
作者
Masson, JF [1 ]
Barnhart, M
Battaglia, TM
Morris, GE
Nieman, RA
Young, PJ
Lorson, CL
Booksh, KS
机构
[1] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
[2] NE Wales Inst, MRIC Biochem Grp, Wrexham LL1 2AW, Wales
[3] Univ Missouri, Dept Vet Pathobiol, Columbia, MO 65211 USA
关键词
D O I
10.1039/b403885a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Spinal muscular atrophy (SMA) is the leading genetic cause of infant mortality. SMA is caused by the homozygous loss of the survival motor neuron 1 (SMN1) gene. A nearly identical copy gene exists known as SMN2, however, due to an aberrant splicing event, the SMN2 gene fails to produce sufficient full-length protein to protect against disease development in the absence of SMN1. While a number of compounds have recently been identified that can stimulate full-length survival motor neuron (SMN) expression from the nearly identical copy SMN2, one of the difficulties has been the lack of a highly reproducible and quantitative means to measure the levels of SMN protein. To develop a technique that allows the rapid and highly sensitive measurement of SMN protein, a Surface Plasmon Resonance (SPR) application has been developed. The ability to quantify unassociated SMN protein and monitor the binding of SMN with other proteins in solution using a SPR sensor in less than 15 min and at low ng mL(-1) levels in HEPES Buffer Saline (HBS) has been achieved. The detection limit for the specific binding of SMN in HBS pH 7.4 solution is 0.99 ng mL(-1) with non-specific binding accounting for approximately 30% of the signal. Quantification of SMN is based on an immunoassay performed on the gold surface of the SPR sensor. 16-mercaptohexadecanoic acid (MHA) was reacted with dicyclohexylcarbodiimide (DCC) and N-hydroxysuccinimide (NHS) to form a pre-activated thiol (MHA-NHS). Antibodies for SMN were then coupled to the sensor with the pre-activated thiol. Sensor specificity was examined with mixtures of myoglobin (MG) and SMN. SMN sensor response decreases by more than 60% when MG was added to SMN. The decrease in sensor response can be attributed to non-specific binding of SMN to MG, verified with a sensor for MG.
引用
收藏
页码:855 / 859
页数:5
相关论文
共 23 条
[1]   The neurobiology of childhood spinal muscular atrophy [J].
Crawford, TO ;
Pardo, CA .
NEUROBIOLOGY OF DISEASE, 1996, 3 (02) :97-110
[2]   Quantitative analyses of SMN1 and SMN2 based on real-time LightCycler PCR:: Fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy [J].
Feldkötter, M ;
Schwarzer, V ;
Wirth, R ;
Wienker, TF ;
Wirth, B .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (02) :358-368
[3]   Correlation between severity and SMN protein level in spinal muscular atrophy [J].
Lefebvre, S ;
Burlet, P ;
Liu, Q ;
Bertrandy, S ;
Clermont, O ;
Munnich, A ;
Dreyfuss, G ;
Melki, J .
NATURE GENETICS, 1997, 16 (03) :265-269
[4]   IDENTIFICATION AND CHARACTERIZATION OF A SPINAL MUSCULAR ATROPHY-DETERMINING GENE [J].
LEFEBVRE, S ;
BURGLEN, L ;
REBOULLET, S ;
CLERMONT, O ;
BURLET, P ;
VIOLLET, L ;
BENICHOU, B ;
CRUAUD, C ;
MILLASSEAU, P ;
ZEVIANI, M ;
LEPASLIER, D ;
FREZAL, J ;
COHEN, D ;
WEISSENBACH, J ;
MUNNICH, A ;
MELKI, J .
CELL, 1995, 80 (01) :155-165
[5]   SMN oligomerization defect correlates with spinal muscular atrophy severity [J].
Lorson, CL ;
Strasswimmer, J ;
Yao, JM ;
Baleja, JD ;
Hahnen, E ;
Wirth, B ;
Le, T ;
Burghes, AHM ;
Androphy, EJ .
NATURE GENETICS, 1998, 19 (01) :63-66
[6]  
LYNN M, 1975, IMMOBILIZED ENZYMES
[7]  
MAN NT, 1996, EPITOPE MAPPING PROT, P377
[8]   Sensitive and real-time fiber-optic-based surface plasmon resonance sensors for myoglobin and cardiac troponin I [J].
Masson, JF ;
Obando, L ;
Beaudoin, S ;
Booksh, K .
TALANTA, 2004, 62 (05) :865-870
[9]  
MASSON JF, 2004, UNPUB ANAL CHEM
[10]  
MASSON JF, 2004, TALANTA