Leippe Philipp, Koehler Leman Julia, Trauner Dirk
Department of Chemistry and Center for Integrated Protein Science Munich, Ludwig-Maximilians-Universität München , Butenandtstrasse 5-13, 81377 Munich, Germany.
Center for Computational Biology, Flatiron Institute, Simons Foundation , 162 Fifth Avenue, New York, New York 10010, United States.
Biochemistry. 2017 Oct 3;56(39):5214-5220. doi: 10.1021/acs.biochem.7b00687. Epub 2017 Sep 14.
Genetics and pharmacology are often seen as two distinct approaches to interrogating, elucidating, and manipulating biological systems. The former is renowned for its precision whereas the latter for its fast kinetics, reversibility, and practicality. Here, we show that both can be joined as "tethered pharmacology", wherein a genetically programmed bioconjugation site provides selectivity and a tethered pharmacophore provides function. The speed of onset, and especially cessation, of pharmacological activity can be greatly enhanced by incorporating photoswitches and using light as the trigger ("tethered photopharmacology"). Genetically encoded, tethered photopharmacology is a variant of optogenetics and could even play a role in medicine wherever gene therapy is viable. However, gene therapy may not be necessary if sufficiently selective tethering strategies that operate on wild-type receptors can be developed.
遗传学和药理学通常被视为研究、阐明和操纵生物系统的两种不同方法。前者以其精确性而闻名,而后者则以其快速动力学、可逆性和实用性著称。在此,我们表明两者可以结合成“拴系药理学”,其中基因编程的生物共轭位点提供选择性,而拴系的药效基团提供功能。通过引入光开关并利用光作为触发因素(“拴系光药理学”),药理活性的起效速度,尤其是终止速度可以大大提高。基因编码的拴系光药理学是光遗传学的一种变体,甚至在基因治疗可行的任何医学领域都可能发挥作用。然而,如果能够开发出对野生型受体起作用的足够选择性的拴系策略,可能就不需要基因治疗了。