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Titolo: USE OF NONRADIOACTIVE LABELS FOR HALF-LIFE MEASUREMENT OF SEX HORMONE-BINDING GLOBULIN IN THE RABBIT
Autore: FIMBEL S; DECHAUD H; GRENOT C; TABARD L; CLAUSTRAT F; BADOR R; PUGEAT M;
- Indirizzi:
- HOP ANTIQUAILLE,CLIN ENDOCRINOL LAB F-69321 LYON 05 FRANCE HOP ANTIQUAILLE,CLIN ENDOCRINOL LAB F-69321 LYON 05 FRANCE HOP ANTIQUAILLE,CENT BIOCHIM LAB F-69321 LYON 05 FRANCE HOP DEBROUSSE,INSERM,U329 F-69322 LYON FRANCE UNIV LYON 1,FAC PHARM,BIOPHYS LAB F-69365 LYON FRANCE
- Titolo Testata:
- Steroids
fascicolo: 10,
volume: 60,
anno: 1995,
pagine: 686 - 692
- SICI:
- 0039-128X(1995)60:10<686:UONLFH>2.0.ZU;2-Y
- Fonte:
- ISI
- Lingua:
- ENG
- Soggetto:
- DTPA-COUPLED ANTIBODIES; IMMUNOFLUOROMETRIC ASSAY; PROTEIN SBP; TESTOSTERONE; RAT; CLEARANCE; ESTRADIOL; SERUM; ACID; IMMUNOASSAYS;
- Keywords:
- SEX HORMONE-BINDING GLOBULIN (SHBG); METABOLIC CLEARANCE RATE; AVIDIN-BIOTIN; EUROPIUM; DIOXETANE-CHEMILUMINESCENCE;
- Tipo documento:
- Article
- Natura:
- Periodico
- Settore Disciplinare:
- Science Citation Index Expanded
- Science Citation Index Expanded
- Citazioni:
- 36
- Recensione:
- Indirizzi per estratti:
-
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- Citazione:
- S. Fimbel et al., "USE OF NONRADIOACTIVE LABELS FOR HALF-LIFE MEASUREMENT OF SEX HORMONE-BINDING GLOBULIN IN THE RABBIT", Steroids, 60(10), 1995, pp. 686-692
Abstract
The purpose of this study was to investigate two methods for labelingrabbit sex hormone-binding globulin (rSHBG) with non-radioactive material, biotin (B) and europium (Eu3+), in order to obtain stable labeled SHBG and measure in vivo its metabolism and distribution. The obtained half-life values were compared with [I-125]rSHBG half-lives. rSHBG was first isolated by immunoaffinity chromatography using an immobilized monoclonal anti-human SHBG (hSHBG) antibody that cross-reacts with rSHBG. This purified rSHBG was labeled by either biotin-X-N-hydroxysuccinimide ester (rSHBG-B), Eu3+-diethylenetriaminepentaacetic dianhydride, or isothiocyanatobenzyldiethylenetriamine-tetraacetic acid reagents (rSHBG-Eu3+) or by I-125 using Bolton and Hunter reagent ([I-125]rSHBG). The labeling procedure preserved the main properties of native SHBG: interaction with the lectine concanavaline A-Sepharose, recognition by anti-hSHBG monoclonal antibody, and, although lower than in native SHBG, the binding affinity for 5 alpha-dihydrotestosterone. These characteristics were the prerequisite for reliable measurement of the metabolism of labeled SHBG, Labeled rSHBG was injected into various rabbits with blood sampling at 2 min and at 1, 2, 4, 8, 12, 24, 48, 72, and 96 h after injection. rSHBC-B or desialylated rSHBG-B and rSHBG-Eu3were captured from serum samples by tubes coated with anti-hSHBG antibody prior to the following detection procedure: biotin was detected by luminometry with the [streptavidin-alkaline phosphatase-dioxetane (AMPPD)] system and europium by time-resolved fluorimetry. [I-125]rSHBG was detected by measurement of radioactivity either directly on serum or after fixation on concanavaline A-Sepharose. The half-life values obtained with rSHBG-B (t(1/2)alpha = 5.5 +/- 0.6 h; t(1/2)beta = 34.8 +/- 5.0 h; n = 4) were comparable to those obtained with [I-125]rSHBG (t(1/2)alpha = 4.5 and 4.0 h; t(1/2)beta = 36.0 and 37.0 h). As previously described for many glycoproteins, treatment of rSHBG-B by neuraminidase induced a dramatic decrease in the half-life of this asialo-rSHBG preparation (t(1/2)alpha = 7.0 and 8.0 min; t(1/2)beta = 4.0 and 4.0h). The shouter half-life observed with rSHBG-Eu3+ could be explainedby the release of europium from the chelates in vitro and probably invivo. In conclusion, biotinylated SHBG is a stable protein with the main characteristics of native SHBG and provides greater detection sensitivity when coupled to a streptavidin-alkaline phosphatase-AMPPD chemiluminescent detection system. The labeling with biotin should be a useful tool for investigating metabolism and specific uptake in target tissue of various forms of recombinant SHBG.
ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 15/01/21 alle ore 16:10:33