Rab7: NMR and kinetics analysis of intact and C-terminal truncated constructs

• Published in: Proteins, structure, function, and bioinformatics structure, function, and bioinformatics, 1997-02, Vol.27 (2), p.204-209
• Main Authors: Neu, Margarete, Brachvogel, Volker, Oschkinat, Hartmut, Zerial, Marino, Metcalf, Peter
• Format: Article
• Language: English
• Subjects: crystal; GTP-Binding Proteins - chemistry; GTP-Binding Proteins - genetics; GTP-Binding Proteins - isolation & purification; GTPase; Kinetics; Magnetic Resonance Spectroscopy; NMR; rab GTP-Binding Proteins; rab7; Recombinant Fusion Proteins - chemistry; Recombinant Fusion Proteins - genetics; Recombinant Fusion Proteins - isolation & purification; targeting; vesicle
• ISSN: 0887-3585; 1097-0134
• DOI: 10.1002/(SICI)1097-0134(199702)27:2<204::AID-PROT6>3.0.CO;2-F

Rab proteins are a family of ˜25kD ras‐related GTPases which are associated with distinct intracellular membranes where they control vesicle traffic between intracellular compartments. The late‐endosomal rab protein rab71–207, (lacking only the C‐terminal lipids of the native molecule) and three C‐terminal truncated constructs rab71–202, rab71–197and rab71–182were purified using an E. coli expression system. The C‐terminal tail region of rab proteins is of special interest because it is thought to target rab proteins to particular intracellular membranes. A comparison of TOCSY‐NMR spectra from intact rab71–207and the tail‐less construct rab71–182suggested that much of the C‐terminal tail is flexible in solution. The GTP hydrolysis, and GDP association and dissociation rates for all the truncated and intact constructs were similar, showing that the tail region of rab71–207has little influence on the hydrolysis and exchange rates of the nucleotide. © 1997 Wiley‐Liss, Inc.