Non-Langmuir kinetics of DNA surface hybridization
Non-Langmuir kinetics of DNA surface hybridization
Abstract Hybridization of complementary single strands of DNA represents a very effective natural molecular recognition process widely exploited for diagnostic, biotechnology and nanotechnology applications. A common approach relies on the immobilization on a surface of single stranded DNA probes that bind complementary targets in solution. However, despite the deep knowledge on DNA interactions in bulk solution, the modelling of the same interactions on a surface are still challenging and perceived as strongly system-dependent. Here we show that a two dimensional analysis of the kinetics of hybridization, performed at different target concentration and probe surface density by a label-free optical biosensor, reveals peculiar features inconsistent with an ideal Langmuir-like behaviour. We propose a simple non-Langmuir kinetic model accounting for an enhanced electrostatic repulsion originating from the surface immobilization of nucleic acids and for steric hindrance close to full hybridization of the surface probes. The analysis of the kinetic data by the model enables to quantify the repulsive potential at the surface, as well as to retrieve the kinetic parameters of isolated probes. We show that the strength and the kinetics of hybridization at large probe density can be improved by a 3D immobilization strategy of probe strands with a double stranded linker. Statement of SignificanceHybridization of nucleic acids strands with complementary sequences is a fundamental biological process and is also widely exploited for diagnostic purposes. Despite the availability of effective models for the equilibrium strength of freely diffusing strands, a general predictive model for surface hybridization is still missing. Moreover, the kinetics of hybridization is not fully understood neither in solution nor on a surface. In this work we show that the analysis of the kinetics of hybridization on a surface reveals and enables to quantify two main additional contributions: electrostatic repulsion and steric hindrance. These are general effects expected to occur not only on a surface but in any condition with large density of nucleic acids, comparable to that of the cellular nucleus.
Casiraghi L.、Buscaglia M.、Vanjur L.、Zanchetta G.、Carzaniga T.、Chiari M.
Universit¨¤ degli Studi di MilanoUniversity of MilanUniversit¨¤ degli Studi di MilanoUniversit¨¤ degli Studi di MilanoUniversit¨¤ degli Studi di MilanoConsiglio Nazionale delle Ricerche
生物物理学分子生物学生物科学现状、生物科学发展
Casiraghi L.,Buscaglia M.,Vanjur L.,Zanchetta G.,Carzaniga T.,Chiari M..Non-Langmuir kinetics of DNA surface hybridization[EB/OL].(2025-03-28)[2025-07-02].https://www.biorxiv.org/content/10.1101/2020.02.27.968081.点此复制
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