Koch Tad H, Smith Drew, Tabacman Eduardo, Zichi Dominic A
Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO 80309-0215, USA.
J Mol Biol. 2004 Mar 5;336(5):1159-73. doi: 10.1016/j.jmb.2004.01.001.
ssDNA oligonucleotides containing bromodeoxyuridine, BrdU-photoaptamers, are rapidly emerging as specific protein capture reagents in protein microarray technologies. A mathematical model for the kinetic analysis of photoaptamer-protein photocross-linking reactions is presented. The model is based on specific aptamer/protein binding followed by laser excitation that can lead to either covalent cross-linking of the photoaptamer and protein in the complex or irreversible photodamage to the aptamer. Two distinct kinetic regimes, (1) frozen and (2) rapid equilibrium, are developed analytically to model binding kinetics between laser pulses. The models are used to characterize the photocross-linking between three photoaptamers and their cognate protein targets; photoaptamers 0650 and 0615 cross-link human basic fibroblast growth factor and 0518 cross-links HIV MN envelope glycoprotein. Data for cross-linking reaction yields as a function of both laser energy dose and target protein concentration are analyzed for affinity constants and cross-link reaction rates. The binding dissociation constants derived from the cross-linking data are in good accord with independent measurements; the rapid equilibrium model appears to produce results more consistent with the experimental observations, although there is significant overlap between the two models for most conditions explored here. The rate of photodamage for 0615 and 0518 is 3.5 and 2.5 times that of the specific cross-link, giving low maximum reaction yields of approximately 20% and approximately 30%, whereas 0650 cross-links with a rate over five times higher than its photodamage rate and has a maximum reaction yield exceeding 80%. Quantum yields for the three systems are estimated from the data; photoaptamer 0650 has a reasonably high quantum yield of approximately 0.2 for protein cross-linking, while 0518 and 0615 have quantum yields of 0.07 and 0.02. The work presented here provides a useful set of metrics that allow for refinement of photoaptamer properties.
含有溴脱氧尿苷的单链DNA寡核苷酸,即BrdU光适配体,正迅速成为蛋白质微阵列技术中特异性蛋白质捕获试剂。本文提出了一种用于光适配体 - 蛋白质光交联反应动力学分析的数学模型。该模型基于特异性适配体/蛋白质结合,随后进行激光激发,这可能导致复合物中光适配体与蛋白质的共价交联或适配体的不可逆光损伤。通过分析得出两种不同的动力学机制,即(1)冻结和(2)快速平衡,以模拟激光脉冲之间的结合动力学。这些模型用于表征三种光适配体与其同源蛋白质靶标的光交联;光适配体0650和0615交联人碱性成纤维细胞生长因子,0518交联HIV MN包膜糖蛋白。分析了交联反应产率随激光能量剂量和靶蛋白浓度变化的数据,以得出亲和常数和交联反应速率。从交联数据得出的结合解离常数与独立测量结果吻合良好;快速平衡模型似乎产生的结果与实验观察结果更一致,尽管在此探索的大多数条件下两种模型之间存在显著重叠。0615和0518的光损伤速率分别是特异性交联速率的3.5倍和2.5倍,最大反应产率较低,分别约为20%和约30%,而0650的交联速率比其光损伤速率高五倍以上,最大反应产率超过80%。根据数据估算了这三个系统的量子产率;光适配体0650的蛋白质交联量子产率约为0.2,相当高,而0518和0615的量子产率分别为0.07和0.02。本文的工作提供了一组有用的指标,可用于优化光适配体的性质。