Geng Steven B, Wu Jiemin, Alam Magfur E, Schultz Jason S, Dickinson Craig D, Seminer Carly R, Tessier Peter M
Isermann Department of Chemical & Biological Engineering, Center for Biotechnology & Interdisciplinary Studies, Rensselaer Polytechnic Institute , Troy, New York 12180, United States.
Eli Lilly Biotechnology Center , San Diego, California 92121, United States.
Bioconjug Chem. 2016 Oct 19;27(10):2287-2300. doi: 10.1021/acs.bioconjchem.6b00207. Epub 2016 Sep 16.
Protein-nanoparticle conjugates are widely used for conventional applications such as immunohistochemistry and biomolecular detection as well as emerging applications such as therapeutics and advanced materials. Nevertheless, it remains challenging to reproducibly prepare stable protein-nanoparticle conjugates with highly similar optical properties. Here we report an improved physisorption method for reproducibly preparing stable antibody-gold conjugates at acidic pH using polyclonal antibodies from a wide range of species (human, goat, rabbit, mouse, and rat). We find that gold particles synthesized using citrate alone or in combination with tannic acid are similar in size but display variable colloidal stability when conjugated to polyclonal antibodies. The variability in conjugate stability is due to differences in the pH and composition of the original gold colloid, which prevents reproducible preparation of stable antibody conjugates without additional purification of the particles prior to conjugation. Sedimentation-based purification of gold particles synthesized using different methods enabled reproducible generation of antibody-gold conjugates with high stability and similar plasmon wavelengths. We also find that antibody conjugates prepared using our improved procedure display excellent performance when applied to a high-throughput immunogold assay (affinity-capture self-interaction nanoparticle spectroscopy, AC-SINS) for identifying monoclonal antibodies with low self-association, high solubility, and low viscosity. The stable antibody conjugates prepared with various types of gold colloid result in robust and reproducible AC-SINS measurements of antibody self-association using extremely dilute (microgram per mL) and unpurified antibody solutions. We expect that this improved methodology will be useful for reproducibly preparing stable antibody-gold conjugates for diverse applications.
蛋白质-纳米颗粒缀合物广泛应用于传统应用,如免疫组织化学和生物分子检测,以及新兴应用,如治疗学和先进材料。然而,可重复地制备具有高度相似光学性质的稳定蛋白质-纳米颗粒缀合物仍然具有挑战性。在此,我们报告一种改进的物理吸附方法,用于在酸性pH条件下使用来自多种物种(人、山羊、兔子、小鼠和大鼠)的多克隆抗体可重复地制备稳定的抗体-金缀合物。我们发现,单独使用柠檬酸盐或与单宁酸结合合成的金颗粒大小相似,但与多克隆抗体缀合时显示出可变的胶体稳定性。缀合物稳定性的差异是由于原始金胶体的pH和组成不同,这使得在缀合前不进行颗粒的额外纯化就无法可重复地制备稳定的抗体缀合物。基于沉降的不同方法合成的金颗粒的纯化能够可重复地产生具有高稳定性和相似等离子体波长的抗体-金缀合物。我们还发现,使用我们改进的方法制备的抗体缀合物在应用于高通量免疫金测定(亲和捕获自相互作用纳米颗粒光谱法,AC-SINS)以鉴定具有低自缔合、高溶解度和低粘度的单克隆抗体时表现出优异的性能。用各种类型的金胶体制备的稳定抗体缀合物使用极稀(每毫升微克)和未纯化的抗体溶液对抗体自缔合进行稳健且可重复的AC-SINS测量。我们预计这种改进的方法将有助于可重复地制备用于各种应用的稳定抗体-金缀合物。