| Literature DB >> 16473593 |
Justin D Topp, Darren S Carney, Bruce F Horazdovsky.
Abstract
Alsin is the gene product mutated in three juvenile-onset neurodegenerative disorders including amyotrophic lateral sclerosis 2 (ALS2). Sequence motif searches within Alsin predict the presence of Vps9, DH, and PH domains, implying that Alsin may function as a guanine nucleotide exchange factor (GEF) for Rab5 and a member of the Rho GTPase family. Procedures are presented in this chapter for the expression, purification, and biochemical characterization of the individual GEF domains of Alsin. A fractionation method is also described for the determination of Alsin's subcellular distribution. The presence of both Rac1 and Rab5 GEF activities makes Alsin a unique dual exchange factor that may couple endocytosis (via Rab5 activation) to cytoskeletal modulation (via Rac1 activation).Entities:
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Year: 2005 PMID: 16473593 DOI: 10.1016/S0076-6879(05)03022-3
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600