Division of Life Science, Hong Kong University of Science and Technology, Clear Water Bay, HKSAR, China.
Biofouling. 2013;29(4):381-400. doi: 10.1080/08927014.2013.776546.
Various antifouling (AF) coatings have been developed to protect submerged surfaces by deterring the settlement of the colonizing stages of fouling organisms. A review of the literature shows that effective AF compounds with specific targets are ones often considered non-toxic. Such compounds act variously on ion channels, quorum sensing systems, neurotransmitters, production/release of adhesive, and specific enzymes that regulate energy production or primary metabolism. In contrast, AF compounds with general targets may or may not act through toxic mechanisms. These compounds affect a variety of biological activities including algal photosynthesis, energy production, stress responses, genotoxic damage, immunosuppressed protein expression, oxidation, neurotransmission, surface chemistry, the formation of biofilms, and adhesive production/release. Among all the targets, adhesive production/release is the most common, possibly due to a more extensive research effort in this area. Overall, the specific molecular targets and the molecular mechanisms of most AF compounds have not been identified. Thus, the information available is insufficient to draw firm conclusions about the types of molecular targets to be used as sensitive biomarkers for future design and screening of compounds with AF potential. In this review, the relevant advantages and disadvantages of the molecular tools available for studying the molecular targets of AF compounds are highlighted briefly and the molecular mechanisms of the AF compounds, which are largely a source of speculation in the literature, are discussed.
各种防污(AF)涂料已被开发出来,通过阻止附着生物定殖阶段的定居来保护水下表面。文献综述表明,具有特定靶标的有效 AF 化合物通常被认为是无毒的。这些化合物作用于离子通道、群体感应系统、神经递质、粘性的产生/释放以及调节能量产生或初级代谢的特定酶。相比之下,具有通用靶标的 AF 化合物可能通过有毒机制起作用,也可能不通过有毒机制起作用。这些化合物影响多种生物活性,包括藻类光合作用、能量产生、应激反应、遗传毒性损伤、免疫抑制蛋白表达、氧化、神经传递、表面化学、生物膜形成和粘性的产生/释放。在所有的靶点中,粘性的产生/释放是最常见的,可能是因为在这个领域进行了更广泛的研究。总体而言,大多数 AF 化合物的特定分子靶标和分子机制尚未确定。因此,现有信息不足以得出关于用作未来具有 AF 潜力的化合物的设计和筛选的敏感生物标志物的分子靶标的类型的明确结论。在这篇综述中,简要强调了研究 AF 化合物分子靶标时可用的分子工具的相关优缺点,并讨论了 AF 化合物的分子机制,这些机制在文献中主要是推测性的。