A luminescent ruthenium complex for ultrasensitive detection of proteins immobilized on membrane supports

被引:125
作者
Berggren, K
Steinberg, TH
Lauber, WM
Carroll, JA
Lopez, MF
Chernokalskaya, E
Zieske, L
Diwu, ZJ
Haugland, RP
Patton, WF
机构
[1] Mol Probes Inc, Bioanalyt Assay Dev Grp, Eugene, OR 97402 USA
[2] Monsanto Co, St Louis, MO 63198 USA
[3] Genomic Solut Inc, Chelmsford, MA 01824 USA
[4] PE Biosyst, Foster City, CA 94404 USA
关键词
protein stain; electroblot; mass spectrometry; fluorescence; ruthenium;
D O I
10.1006/abio.1999.4364
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
SYPRO Ruby protein blot stain provides a sensitive, gentle, fluorescence-based method for detecting proteins on nitrocellulose or polyvinylidene difluoride (PVDF) membranes. SYPRO Ruby dye is a permanent stain composed of ruthenium as part of an organic complex that interacts noncovalently with proteins. Stained proteins can be excited by ultraviolet light of about 302 nm or with visible light of about 470 nm. Fluorescence emission of the dye is approximately 618 nm. The stain can be visualized using a wide range of excitation sources utilized in image analysis systems including a UV-B transilluminator, 488-nm argon-ion laser, 532-nm yttrium-aluminum-garnet (YAG) laser, blue fluorescent light bulb, or blue light-emitting diode (LED). The detection sensitivity of SYPRO Ruby protein blot stain (0.25-1 ng protein/mm(2)) is superior to that of amido black, Coomassie blue, and india ink staining and nearly matches colloidal gold staining. SYPRO Ruby protein blot stain visualizes proteins more rapidly than colloidal gold stain and the linear dynamic range is more extensive. Unlike colloidal gold stain, SYPRO Ruby protein blot stain is fully compatible with subsequent biochemical applications including colorimetric and chemiluminescent immunoblotting, Edman-based sequencing and mass spectrometry. (C) 1999 Academic Press.
引用
收藏
页码:129 / 143
页数:15
相关论文
共 40 条
[1]   Nonenzymatic chemiluminescent detection and quantitation of total protein on Western and slot blots allowing subsequent immunodetection and sequencing [J].
Alba, FJ ;
Daban, JR .
ELECTROPHORESIS, 1997, 18 (11) :1960-1966
[2]   Rapid fluorescent monitoring of total protein patterns on sodium dodecyl sulfate-polyacrylamide gels and Western blots before immunodetection and sequencing [J].
Alba, FJ ;
Daban, JR .
ELECTROPHORESIS, 1998, 19 (14) :2407-2411
[3]  
[Anonymous], 1988, Antibodies: A Laboratory Manual
[4]   A HIGH-AFFINITY PROTEIN STAIN FOR WESTERN BLOTS, TISSUE PRINTS, AND ELECTROPHORETIC GELS [J].
BICKAR, D ;
REID, PD .
ANALYTICAL BIOCHEMISTRY, 1992, 203 (01) :109-115
[5]   A nonradioactive double detection method for the assignment of spots in two-dimensional blots [J].
Chevallet, M ;
Procaccio, V ;
Rabilloud, T .
ANALYTICAL BIOCHEMISTRY, 1997, 251 (01) :69-72
[6]   COMPARISON OF DIFFERENT STAINING METHODS FOR POLYVINYLIDENE DIFLUORIDE MEMBRANES [J].
CHRISTIANSEN, J ;
HOUEN, G .
ELECTROPHORESIS, 1992, 13 (03) :179-183
[7]  
Dunn MJ, 1999, METH MOL B, V112, P313
[8]   COLLOIDAL GOLD STAINING AND IMMUNOPROBING OF PROTEINS ON THE SAME NITROCELLULOSE BLOT [J].
EGGER, D ;
BIENZ, K .
ANALYTICAL BIOCHEMISTRY, 1987, 166 (02) :413-417
[9]  
Fowler S J, 1994, Methods Mol Biol, V32, P239
[10]   Peptide-mass profiles of polyvinylidene difluoride-bound proteins by matrix-assisted laser desorption ionization time-of-flight mass spectrometry in the presence of nonionic detergents [J].
Gharahdaghi, F ;
Kirchner, M ;
Fernandez, J ;
Mische, SM .
ANALYTICAL BIOCHEMISTRY, 1996, 233 (01) :94-99