PURIFICATION OF THE GROWTH-ASSOCIATED PROTEIN GAP-43 BY REVERSED PHASE CHROMATOGRAPHY - AMINO-ACID-SEQUENCE ANALYSIS AND CDNA IDENTIFICATION

被引:17
作者
CHANGELIAN, PS [1 ]
MEIRI, K [1 ]
SOPPET, D [1 ]
VALENZA, H [1 ]
LOEWY, A [1 ]
WILLARD, M [1 ]
机构
[1] WASHINGTON UNIV,SCH MED,DEPT ANAT & NEUROBIOL,660 S EUCLID AVE,ST LOUIS,MO 63110
关键词
cDNA cloning; GAP-43; Nerve regeneration; Protein purification; Protein turnover;
D O I
10.1016/0006-8993(90)91376-R
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
GAP-43 is a neuronal phosphoprotein. Increased synthesis and axonal transport of GAP-43 has been associated with axon growth, and altered phosphorylation of GAP-43 has been associated with changes in synaptic efficacy. Here we report a rapid and effective procedure employing reverse-phase HPLC for the purification of GAP-43 from rat brain. To characterize the protein purified by this procedure, we generated proteolytic fragments and determined their amino acid sequences. These directly determined sequences, corresponding to 56% of the GAP-43 amino acids, confirm recently reported sequences deduced from the nucleotide sequences of cDNAs. Using oligonucleotide probes constructed according to these amino acid sequences, we identified GAP-43 cDNAs in a library prepared from neonatal rat superior cervical ganglion cells. One of these cDNAs was 1.1 kB in size; it hybridized specifically with a 1.5 kB RNA from brain, but not from liver, and contained the entire coding sequence for GAP-43. This cDNA differed from recently reported cDNAs in its 3′ untranslated region. © 1990.
引用
收藏
页码:259 / 268
页数:10
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