Department of Chemistry, McNeese State University, Lake Charles, Louisiana, 70609, USA.
Department of Chemistry, McNeese State University, Lake Charles, Louisiana, 70609, USA.
Comp Biochem Physiol Part D Genomics Proteomics. 2009 Dec;4(4):300-304. doi: 10.1016/j.cbd.2009.08.001. Epub 2009 Aug 23.
Blood was collected from three juvenile alligators (Alligator mississippiensis) before, and again 24h after, injection with bacterial lipopolysaccharide (LPS). The leukocytes were collected from both samples, and the proteins were extracted. Each group of proteins was labeled with a different fluorescent dye and the differences in protein expression were analyzed by two dimensional differential in-gel expressions (2D-DIGE). The proteins which appeared to be increased or decreased by treatment with LPS were selected and analyzed by MALDI-TOF to determine mass and LC-MS/MS to acquire the partial protein sequences. The peptide sequences were compared to the NCBI protein sequence database to determine homology with other sequences from other species. Several proteins of interest appeared to be increased upon LPS stimulation. Proteins with homology to human transgelin-2, fish glucose-6-phosphate dehydrogenase, amphibian α-enolase, alligator lactate dehydrogenase, fish ubiquitin-activating enzyme, and fungal β-tubulin were also increased after LPS injection. Proteins with homology to fish vimentin 4, murine heterogeneous nuclear ribonucleoprotein A3, and avian calreticulin were found to be decreased in response to LPS. In addition, five proteins, four of which were up-regulated (827, 560, 512, and 650%) and one that exhibited repressed expression (307%), did not show homology to any protein in the database, and thus may represent newly discovered proteins. We are using this biochemical approach to isolate and characterize alligator proteins with potential relevant immune function.
从三只幼年短吻鳄(Alligator mississippiensis)中采集血液,分别在注射细菌脂多糖(LPS)之前和之后 24 小时采集。从这两个样本中收集白细胞,并提取蛋白质。将每组蛋白质用不同的荧光染料标记,并通过二维差异凝胶电泳(2D-DIGE)分析蛋白质表达的差异。选择那些似乎因 LPS 处理而增加或减少的蛋白质,通过 MALDI-TOF 确定质量,通过 LC-MS/MS 获取部分蛋白质序列。将肽序列与 NCBI 蛋白质序列数据库进行比较,以确定与其他物种序列的同源性。一些似乎在 LPS 刺激下增加的感兴趣的蛋白质。与人类转凝胶素-2、鱼类葡萄糖-6-磷酸脱氢酶、两栖类α-烯醇酶、短吻鳄乳酸脱氢酶、鱼类泛素激活酶和真菌β-微管蛋白同源的蛋白质在 LPS 注射后也增加。与鱼类波形蛋白 4、鼠异质性核核糖核蛋白 A3 和禽类钙网蛋白同源的蛋白质在 LPS 作用下减少。此外,有 5 种蛋白质,其中 4 种上调(827、560、512 和 650%),1 种下调(307%),与数据库中的任何蛋白质均无同源性,因此可能代表新发现的蛋白质。我们正在使用这种生化方法分离和鉴定具有潜在相关免疫功能的短吻鳄蛋白质。