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Photolabeling of the phosphate binding site of chloroplast coupling factor 1 With [32P]azidonitrophenyl phosphate
[摘要]

Chloroplast F1-AT Pase (CF1) was photolabeled by a radiolabeled photoactivatable derivative of Pi, 4-azido-2-nitrophenyl [32P]phosphate (ANPP). The radioactivity was localized in the β subunit of CF1. Upon cleavage of the β subunit by cyanogen bromide, the predominantly labeled peptide was recovered, which was subsequently subjected to tryptic digestion. A tryptic peptide (spanning Ile312-Arg354), was found to contain nearly all the covalently bound radioactivity. By Edman degradation, the labeled amino acid residues were identified as Tyr328, Val329 and Pro330. The labeled β-Tyr328 of CF1 is the equivalent of β-Tyr311 of F1 from beef heart mitochondria, which was previously found to be photolabeled by ANPP [J. Garin et al. (1989) Biochemistry 28, 1442–1448].

[发布日期]  [发布机构] 
[效力级别]  [学科分类] 生物化学/生物物理
[关键词] Chloroplast F1 ATPase;Phosphate binding site;Photoaffinity;4-Azido-2-nitrophenylphosphate;ANPP;4-azido-2-nitrophenyl phospate;MES;2-(N-morpholino)ethane sulfonic acids;TFA;trifluoroacetic acid;CF1;catalytic factor (soluble) of the ATP systhase complex from chloroplasts;TDAB;tetradecyltrimethylammonium bromide;EDC;1-ethyl-3-(3-dimethyl-aminopropyl) carbodiimide [时效性] 
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