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天冬氨酸83、谷氨酸113和谷氨酸134不专门参与牛视紫红质中席夫碱质子化或波长调节。

Asp83, Glu113 and Glu134 are not specifically involved in Schiff base protonation or wavelength regulation in bovine rhodopsin.

作者信息

Janssen J J, De Caluwé G L, De Grip W J

机构信息

Department of Biochemistry, University of Nijmegen, The Netherlands.

出版信息

FEBS Lett. 1990 Jan 15;260(1):113-8. doi: 10.1016/0014-5793(90)80080-3.

Abstract

Site-specific mutagenesis was employed to investigate the proposed contribution of proton-donating residues (Glu, Asp) in the membrane domains of bovine rhodopsin to protonation of the Schiff base-linking protein and chromophore or to wavelength modulation of this visual pigment. Three point-mutations were introduced to replace the highly conserved residues Asp83 by Asn (D83N), Glu113 by Gln (E113 Q) or Glu134 by Asp (E134D), respectively. All 3 substitutions had only marginal effects on the spectral properties of the final pigment (less than or equal to 3 nm blue-shift relative to native rhodopsin). Hence, none of these residues by itself is specifically involved in Schiff base protonation or wavelength modulation of bovine rhodopsin.

摘要

采用位点特异性诱变来研究牛视紫红质膜结构域中质子供体残基(Glu、Asp)对席夫碱连接蛋白和发色团质子化或对视色素波长调制的潜在贡献。分别引入三个点突变,将高度保守的残基Asp83替换为Asn(D83N)、Glu113替换为Gln(E113Q)或Glu134替换为Asp(E134D)。所有这3种取代对最终色素的光谱特性只有微小影响(相对于天然视紫红质,蓝移小于或等于3纳米)。因此,这些残基单独都不特别参与牛视紫红质的席夫碱质子化或波长调制。

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