Liu Dandan, Viennois Emilie, Fang Jieqiong, Merlin Didier, Iyer Suri S
Department of Chemistry, Georgia State University, 788 Petit Science Center, Atlanta, Georgia 30302, United States.
Institute for Biomedical Sciences, Georgia State University, 790 Petit Science Center, Atlanta, Georgia 30302, United States.
ACS Omega. 2021 Mar 3;6(10):6582-6587. doi: 10.1021/acsomega.0c05115. eCollection 2021 Mar 16.
We have investigated the association of matrix metallopeptidase 9 (MMP-9) and tumor necrosis factor α (TNF-α) levels with colitis severity using an established IL10-/- mouse model, which reflects the severity of inflammation in humans with inflammatory bowel disease (IBD). We found that MMP-9 and TNF-α correlated with colitis severity. In parallel, we developed assays to detect fecal MMP-9 and serum TNF-α using "cap and release" mesoporous silica nanoparticles (MSNs). MMP-9 peptide substrates as "caps" were attached to dye-loaded MSNs. The introduction of MMP-9 resulted in substrate cleavage and subsequent dye release, which was rapidly detected using a fluorometer. For TNF-α, an anti-TNF antibody was used as the "cap". The introduction of TNF-α antigen leads to the release of the dyes because the antigen binds more strongly to the antibody cap. The MSN-based assays can detect MMP-9 and TNF-α effectively, although signal amplification is required to meet clinical sensitivity.
我们使用已建立的IL10 - / - 小鼠模型研究了基质金属蛋白酶9(MMP - 9)和肿瘤坏死因子α(TNF - α)水平与结肠炎严重程度的关联,该模型反映了人类炎症性肠病(IBD)的炎症严重程度。我们发现MMP - 9和TNF - α与结肠炎严重程度相关。同时,我们开发了使用“帽和释放”介孔二氧化硅纳米颗粒(MSN)检测粪便MMP - 9和血清TNF - α的检测方法。作为“帽”的MMP - 9肽底物附着在负载染料的MSN上。引入MMP - 9导致底物裂解并随后释放染料,使用荧光计可快速检测到。对于TNF - α,使用抗TNF抗体作为“帽”。引入TNF - α抗原会导致染料释放,因为抗原与抗体帽结合更紧密。基于MSN的检测方法可以有效检测MMP - 9和TNF - α,尽管需要信号放大以满足临床灵敏度。