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虫荧光素结合位残基 C/T311(S314)通过与氧杂荧光素酚盐的主链相互作用影响甲虫荧光素酶的生物发光颜色。

The luciferin binding site residues C/T311 (S314) influence the bioluminescence color of beetle luciferases through main-chain interaction with oxyluciferin phenolate.

机构信息

Department of Physics, Chemistry and Mathematics, Graduate Program of Biotechnology and Environmental Monitoring, Federal University of São Carlos (UFSCAR), Rodovia João Leme dos Santos, km 110, Itinga, Sorocaba, SP, Brazil.

出版信息

Biochemistry. 2013 Jan 8;52(1):19-27. doi: 10.1021/bi300740y. Epub 2012 Dec 13.

Abstract

Beetle luciferases emit different bioluminescence colors from green to red; however, no clear relationship between the identity of the luciferin binding site residues and bioluminescence colors was found in different luciferases, and it is unclear whether critical interactions affecting emission spectra occur on the thiazolyl or on the benzothiazolyl sides of the luciferin binding site. Through homology modeling and site-directed mutagenesis using our multicolor set of beetle luciferases (Pyrearinus termitilluminans larval click beetle, Pte, λ(max) = 534 nm; Phrixothrix hirtus railroad worm red emitting, PxRE, λ(max) = 623 nm; and Macrolampis sp2 firefly, Mac, λ(max) = 564 nm), we show that the residues C/T311 (S314) play an important role in bioluminescence color determination. Modeling studies indicate that the main-chain carbonyls of these residues are close to both oxyluciferin phenolate and AMP, whereas the side chains pack against second-shell residues. The C311(S314)A mutation considerably red shifts the spectra of the green-yellow-emitting luciferases (Pte λ(max) = 534 to 590 nm; Mac λ(max) = 564 to 583/613 nm) and affects the K(M) values for luciferin and ATP, but not the spectrum of the red-emitting luciferase. On the other hand, whereas the exchange between C/T311 (S314) caused smaller effects on the emission spectra of green-yellow-emitting luciferases, the C311T substitution (naturally found in green-emitting railroad worm luciferases) resulted in the largest reported blue shift in P. hirtus red-emitting luciferase (λ(max) = 623 to 606 nm). Altogether, these results indicate that the stability of residues C/T311 (S314) and the size of the cavity around oxyluciferin phenolate affect bioluminescence colors and suggest, for the first time, the occurrence of a critical interaction between main-chain carbonyls of position 311 (314) residues and oxyluciferin phenolate.

摘要

甲虫荧光素酶发出的生物发光颜色从绿色到红色各不相同;然而,在不同的荧光素酶中,并未发现荧光素结合部位残基的身份与生物发光颜色之间存在明确的关系,也不清楚影响发射光谱的关键相互作用是否发生在荧光素结合部位的噻唑基侧或苯并噻唑基侧。通过使用我们的多色甲虫荧光素酶(Pyrearinus termitilluminans 幼虫叩头甲,Pte,λ(max) = 534nm;Phrixothrix hirtus 铁路蠕虫红色发射,PxRE,λ(max) = 623nm;以及 Macrolampis sp2 萤火虫,Mac,λ(max) = 564nm)进行同源建模和定点突变,我们表明残基 C/T311(S314)在生物发光颜色确定中起重要作用。建模研究表明,这些残基的主链羰基与氧荧光素酚盐和 AMP 都接近,而侧链则与第二壳层残基结合。C311(S314)A 突变使黄绿色发光荧光素酶的光谱显著红移(Pte λ(max) = 534 至 590nm;Mac λ(max) = 564 至 583/613nm),并影响荧光素和 ATP 的 K(M)值,但不影响红色发光荧光素酶的光谱。另一方面,虽然 C/T311(S314)的交换对黄绿色发光荧光素酶的发射光谱影响较小,但 C311T 取代(在绿色发光铁路蠕虫荧光素酶中自然存在)导致 P. hirtus 红色发光荧光素酶报告的最大蓝移(λ(max) = 623 至 606nm)。总之,这些结果表明残基 C/T311(S314)的稳定性和氧荧光素酚盐周围腔的大小影响生物发光颜色,并首次表明位置 311(314)残基的主链羰基与氧荧光素酚盐之间存在关键相互作用。

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