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一种具有靶向能力的光敏融合蛋白。

A photosensitizing fusion protein with targeting capabilities.

机构信息

Dipartimento di Scienze degli Alimenti e del Farmaco, Università degli Studi di Parma, Parma, Italy.

DIFILAB, Dipartimento di Fisica, Università di Genova, Genova, Italy.

出版信息

Biomol Concepts. 2022 Mar 29;13(1):175-182. doi: 10.1515/bmc-2022-0014.

Abstract

The photodynamic treatment for antimicrobial applications or anticancer therapy relies on reactive oxygen species generated by photosensitizing molecules after absorption of visible or near-infrared light. If the photosensitizing molecule is in close vicinity of the microorganism or the malignant cell, a photocytotoxic action is exerted. Therefore, the effectiveness of photosensitizing compounds strongly depends on their capability to target microbial or cancer-specific proteins. In this study, we report on the preparation and preliminary characterization of human recombinant myoglobin fused to the vasoactive intestinal peptide to target vasoactive intestinal peptide receptor (VPAC) receptors. Fe-protoporphyrin IX was replaced by the photosensitizing compound Zn-protoporphyrin IX. Taking advantage of the fluorescence emission by Zn-protoporphyrin IX, we show that the construct can bind prostate cancer cells where the VPAC receptors are expressed.

摘要

光动力疗法在抗菌应用或抗癌治疗方面的应用依赖于光敏分子在吸收可见光或近红外光后产生的活性氧物种。如果光敏分子靠近微生物或恶性细胞,就会产生光细胞毒性作用。因此,光敏化合物的有效性强烈依赖于它们靶向微生物或癌症特异性蛋白的能力。在这项研究中,我们报告了与人重组肌红蛋白融合的血管活性肠肽的制备和初步特性,以靶向血管活性肠肽受体(VPAC)受体。亚铁原卟啉 IX 被光敏化合物锌原卟啉 IX 取代。利用锌原卟啉 IX 的荧光发射,我们表明该构建体可以与表达 VPAC 受体的前列腺癌细胞结合。

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