自由生活巴西负鼠(Didelphis aurita)血清蛋白图谱。

IF 2.5 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
ELECTROPHORESIS Pub Date : 2025-08-23 DOI:10.1002/elps.70016
Andrés Mauricio Ortega Orozco, Lucas Drumond Bento, Pollyanna Cordeiro Souto, Fabrícia Modolo Girardi, Verônica Rodrigues Castro, João Vitor Gonçalves de Oliveira, Camilo José Ramirez Lopez, Edvaldo Barros, Artur Kanadani Campos, Leandro Abreu da Fonseca
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引用次数: 0

摘要

Didelphis aurita是一种广泛分布在巴西东南部的合群有袋类动物,以其对毒液的抵抗力和与生物医学研究的相关性而闻名。本研究的目的是表征自由生活的aurita个体的血清蛋白图谱。研究人员分析了27只动物的血液样本,将它们分为“健康”和“患病”两类。共鉴定出18条蛋白带,分子量在24 ~ 242kda之间。其中,特定波段的变化与健康状况(J波段)、性别(D、M、N和P波段)和年龄(N和P波段)有关。质谱(液相色谱-串联质谱[LC-MS/MS])鉴定出7种蛋白,包括DM64、铜蓝蛋白、血管性血变因子A (VWFA)结构域蛋白、α -2-巨球蛋白、纤维连接蛋白和肌动蛋白解聚因子。这些结果强调了生物因素对血清蛋白谱的影响,并加强了aurita作为免疫学和蛋白质组学研究模型的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum Proteinogram in the Free-Living Brazilian Common Opossum (Didelphis aurita).

Didelphis aurita is a synanthropic marsupial widely distributed in southeastern Brazil, known for its resistance to venom and its relevance in biomedical research. This study aimed to characterize the serum proteinogram of free-living D. aurita individuals. Blood samples from 27 animals, classified as "healthy" or "diseased," were analyzed. Eighteen protein bands were identified, with molecular weights ranging from 24 to 242 kDa. Among these, variations in specific bands were associated with health status (band J), sex (bands D, M, N, and P), and age (bands N and P). Mass spectrometry (liquid chromatography-tandem mass spectrometry [LC-MS/MS]) identified seven proteins, including DM64, ceruloplasmin, von Willebrand factor A (VWFA) domain protein, alpha-2-macroglobulin, fibronectin, and actin depolymerizing factor. These results highlight the influence of biological factors on serum protein profiles and reinforce the potential of D. aurita as a model for immunological and proteomic studies.

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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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