| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
1 Department of OBGYN, Robert Wood Johnson (Rutgers) Medical School, Piscataway, New Jersey 08854, USA
2 Millennium Pharmaceutical Company, Cambridge, Massachusetts 02139, USA
3 Ares Advanced Technology, Randolph, Massachusetts 02368, USA
4 Istituto di Ricerca Cesare Serono S.p.A., Ardea, Italy
Reprint requests to: Dr. William R. Moyle, Department of OBGYN, Robert Wood Johnson (Rutgers) Medical School, 675 Hoes Lane, Piscataway, New Jersey 08854, USA; fax: (732) 235-4225.
Chorionic gonadotropin (hCG) is a heterodimeric placental glycoprotein hormone essential for human reproduction. Twenty hCG ß-subunit residues, termed the seatbelt, are wrapped around 
-subunit loop 2 (2) and their positions "latched" by a disulfide formed by cysteines at the end of the seatbelt (Cys 110) and in the ß-subunit core (Cys 26). This unique arrangement explains the stability of the heterodimer but raises questions as to how the two subunits combine. The seatbelt is latched in the free ß-subunit. If the seatbelt remained latched during the process of subunit combination, formation of the heterodimer would require 2 and its attached oligosaccharide to be threaded through a small ß-subunit hole. The subunits are known to combine during oxidizing conditions in vitro, and studies described here tested the idea that this requires transient disruption of the latch disulfide, possibly as a consequence of the thioredoxin activity reported in hCG. We observed that alkylating agents did not modify either cysteine in the latch disulfide (Cys 26 or Cys 110) during heterodimer formation in several oxidizing conditions and had minimal influence on these cysteines during combination in the presence of mild reductants (1–3 mM ß-mercaptoethanol). Reducing agents appeared to accelerate subunit combination by disrupting a disulfide (Cys 93–Cys 100) that forms a loop within the seatbelt, thereby increasing the size of the ß-subunit hole. We propose a mechanism for hCG assembly in vitro that depends on movements of 2 and the seatbelt and suggest that the process of glycoprotein hormone subunit combination may be useful for studying the movements of loops during protein folding.
Keywords: Glycoprotein hormone subunit combination; gonadotropin; protein folding; hCG
Abbreviations: hCG, human chorionic gonadotropin • NEM, N-ethylmaleimide • IA, iodoacetate • VP, 4-vinylpyridine • SA, streptavidin • MB, 3–(N-maleimidylpropionyl)biocytin • IAEDANS, 5–((((2-iodoacetyl)amino)ethyl)amino)napthalene-1-sulfonic acid.
CiteULike 
Connotea 
Del.icio.us 
Digg 
Reddit 
Technorati What's this?
This article has been cited by other articles:
|
|
 |
|
  S.F. de Medeiros and R.J. Norman Human choriogonadotrophin protein core and sugar branches heterogeneity: basic and clinical insights Hum. Reprod. Update, January 1, 2009; 15(1): 69 - 95. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 W. E. Merz, J.-M. Krause, J. Roig, V. Singh, and P. Berger Nonassembled Human Chorionic Gonadotropin Subunits and {alpha}{alpha}-Homodimers Use Fast-Track Processing in the Secretory Pathway in Contrast to {alpha}{beta}-Heterodimers Endocrinology, December 1, 2007; 148(12): 5831 - 5841. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J.-M. Krause, P. Berger, J. Roig, V. Singh, and W. E. Merz Rapid Maturation of Glycoprotein Hormone Free {alpha}-Subunit (GPH{alpha}) and GPH{alpha}{alpha} Homodimers Mol. Endocrinol., October 1, 2007; 21(10): 2551 - 2564. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S. D. McKenna, G. Feger, C. Kelton, M. Yang, V. Ardissone, R. Cirillo, P.-A. Vitte, X. Jiang, and R. K. Campbell Tumor Necrosis Factor (TNF)-Soluble High-Affinity Receptor Complex as a TNF Antagonist J. Pharmacol. Exp. Ther., August 1, 2007; 322(2): 822 - 828. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
E. Jauniaux, L. Poston, and G. J. Burton Placental-related diseases of pregnancy: involvement of oxidative stress and implications in human evolution Hum. Reprod. Update, November 1, 2006; 12(6): 747 - 755. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 Y. Xing, R. V. Myers, D. Cao, W. Lin, M. Jiang, M. P. Bernard, and W. R. Moyle Glycoprotein Hormone Assembly in the Endoplasmic Reticulum: I. THE GLYCOSYLATED END OF HUMAN {alpha}-SUBUNIT LOOP 2 IS THREADED THROUGH A {beta}-SUBUNIT HOLE J. Biol. Chem., August 20, 2004; 279(34): 35426 - 35436. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. Xing, R. V. Myers, D. Cao, W. Lin, M. Jiang, M. P. Bernard, and W. R. Moyle Glycoprotein Hormone Assembly in the Endoplasmic Reticulum: II. MULTIPLE ROLES OF A REDOX SENSITIVE {beta}-SUBUNIT DISULFIDE SWITCH J. Biol. Chem., August 20, 2004; 279(34): 35437 - 35448. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. Xing, R. V. Myers, D. Cao, W. Lin, M. Jiang, M. P. Bernard, and W. R. Moyle Glycoprotein Hormone Assembly in the Endoplasmic Reticulum: IV. PROBABLE MECHANISM OF SUBUNIT DOCKING AND COMPLETION OF ASSEMBLY J. Biol. Chem., August 20, 2004; 279(34): 35458 - 35468. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
G. B. Fralish, P. Narayan, and D. Puett Consequences of Single-Chain Translation on the Structures of Two Chorionic Gonadotropin Yoked Analogs in {alpha}-{beta} and {beta}-{alpha} Configurations Mol. Endocrinol., April 1, 2003; 17(4): 757 - 767. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Y. Xing, W. Lin, M. Jiang, R. V. Myers, D. Cao, M. P. Bernard, and W. R. Moyle Alternatively Folded Choriogonadotropin Analogs. IMPLICATIONS FOR HORMONE FOLDING AND BIOLOGICAL ACTIVITY J. Biol. Chem., December 7, 2001; 276(50): 46953 - 46960. [Abstract] [Full Text] [PDF]
|
|
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
