Literature DB >> 19999739

Fluorescent thiol reagents. VI. N-(1-Anilinonaphthyl-4)maleimide; a fluorescent hydrophobic probe directed to thiol groups in protein.

Y Kanaoka1, M Machida, M Machida, T Sekine.   

Abstract

N-(1-Anilinonaphthyl-4)maleimide (ANM) (m.p. 207-208.5 degrees C), nonfluorescent, reacts selectively with thiols to give addition products which are strongly fluorescent (excitation maximum 355 nm, emission maximum 448 nm, in ethanol). 0.7 mole of ANM was introduced into thiol groups of egg albumin without modifying any other amino acid residues. In the fluorescence spectra of the reaction products of ANM with thiols, the quantum yields increase and the emission maxima shift towards the blue as the solvent polarity decreases. This remarkable solvent dependence was described in terms ofZ value of the solvents. ANM is thus expected to be a useful fluorescent hydrophobic probe directed to thiol groups in protein.

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Year:  1973        PMID: 19999739

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  4 in total

1.  Characteristic distribution of sulfhydryl groups in human epidermal cancer by the new histochemical staining method.

Authors:  H Ogawa; A Taneda
Journal:  Arch Dermatol Res       Date:  1979-02-23       Impact factor: 3.017

2.  The histochemistry of thiols and disulphides. II. Methodology of differential staining.

Authors:  T O Sippel
Journal:  Histochem J       Date:  1978-09

3.  Histochemical demonstration of thiols and disulfides by the fluorescent labeling agent, monobromobimane: an application to the hypothalamo-neurohypophysial system.

Authors:  H Gainer; N S Kosower
Journal:  Histochemistry       Date:  1980

Review 4.  The chronological evolution of small organic molecular fluorescent probes for thiols.

Authors:  Yongkang Yue; Fangjun Huo; Caixia Yin
Journal:  Chem Sci       Date:  2020-12-15       Impact factor: 9.825

  4 in total

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