Ding Jeak Ling, Ho Bow
Department of Biological Sciences, Faculty of Science, National University of Singapore, 14 Science Drive 4, Singapore, 117543, Singapore.
Subcell Biochem. 2010;53:187-208. doi: 10.1007/978-90-481-9078-2_9.
Gram negative bacterial endotoxin is a biological pyrogen that causes fever when introduced intravenously. The endotoxin, also known as lipopolysaccharide (LPS), is found in the outer membrane of Gram-negative bacteria. During Gram-negative sepsis, endotoxin stimulates host macrophages to release inflammatory cytokines. However, excessive inflammation causes multiple organ failure and death. Endotoxins, which are ubiquitous pathogenic molecules, are a bane to the pharmaceutical industry and healthcare community. Thus early and sensitive detection of endotoxin is crucial to prevent endotoxaemia. The limulus amebocyte lysate (LAL) has been widely used for ~30 years for the detection of endotoxin in the quality assurance of injectable drugs and medical devices. The LAL constitutes a cascade of serine proteases which are triggered by trace levels of endotoxin, culminating in a gel clot at the end of the reaction. The Factor C, which normally exists as a zymogen, is the primer of this coagulation cascade. In vivo, Factor C is the perfect biosensor, which alerts the horseshoe crab of the presence of a Gram-negative invader. The hemostatic end-point entraps the invader, killing it and limiting further infection. However, as an in vitro endotoxin detection tool, variations in the sensitivity and specificity of LAL to endotoxin, and the dwindling supply of horseshoe crabs are posing increasing challenges to the biotechnology industry. This has necessitated the innovation of an alternative test for endotoxin. Thus, Factor C became the obvious, albeit tricky target for the recombinant technology effort. This chapter documents the backwater of mining the natural blood lysate of the endangered species to the monumental effort of genetic engineering, to produce recombinant Factor C (rFC). The rFC is a 132 kDa molecule, which was produced as a proenzyme inducible by the presence of trace levels of endotoxin. The rFC forms the basis of the "PyroGene" kit, which is a novel micro-enzymatic endotoxin diagnostic assay for high-throughput screens of endotoxin. Using the rFC, Lonza Inc. has spawned the "PyroSense" which serves as checkpoints of the biotechnology production line. Thus, from cloning to commercial applications, the rFC has initiated a new era in endotoxin-testing for the quality assurance of biomedical products and for the healthcare industry, whilst sparing the endangered horseshoe crabs.
革兰氏阴性菌内毒素是一种生物致热原,静脉注射时会引起发热。这种内毒素,也被称为脂多糖(LPS),存在于革兰氏阴性菌的外膜中。在革兰氏阴性菌败血症期间,内毒素刺激宿主巨噬细胞释放炎性细胞因子。然而,过度炎症会导致多器官功能衰竭和死亡。内毒素作为普遍存在的致病分子,对制药行业和医疗界来说是一大祸害。因此,早期和灵敏地检测内毒素对于预防内毒素血症至关重要。鲎试剂(LAL)在注射用药物和医疗器械的质量保证中用于检测内毒素已有约30年的历史。LAL构成了一系列丝氨酸蛋白酶,它们由痕量水平的内毒素触发,最终在反应结束时形成凝胶凝块。通常以酶原形式存在的C因子是这种凝血级联反应的起始物。在体内,C因子是完美的生物传感器,能提醒鲎存在革兰氏阴性入侵者。止血终点会困住入侵者,将其杀死并限制进一步感染。然而,作为一种体外内毒素检测工具,LAL对内毒素的敏感性和特异性存在差异,以及鲎的供应日益减少,这给生物技术行业带来了越来越大的挑战。这就需要创新一种替代的内毒素检测方法。因此,C因子成为了重组技术努力的明显(尽管棘手)目标。本章记录了从挖掘濒危物种的天然血液裂解物的默默无闻的工作到基因工程的巨大努力,以生产重组C因子(rFC)的过程。rFC是一种132 kDa的分子,它作为一种在痕量水平内毒素存在时可诱导的酶原产生。rFC构成了“PyroGene”试剂盒的基础,该试剂盒是一种用于高通量筛选内毒素的新型微酶促内毒素诊断测定法。利用rFC,龙沙集团公司推出了“PyroSense”,它可作为生物技术生产线的检查点。因此,从克隆到商业应用,rFC开创了内毒素检测的新时代,用于生物医学产品的质量保证和医疗行业,同时保护了濒危的鲎。