Literature DB >> 19551948

Continuous and quantitative delivery of molecules into individual cells with a diffusional microburet.

Miklós Gratzl1, Chen Yi, Gary R Bright.   

Abstract

Direct delivery of molecules into the cytosol of live cells is required in many areas of biology and clinical research. Molecules of interest include indicator dyes, biomolecules, and pharmacological agents. In this work we describe continuous delivery of molecules into single cells using a diffusional microburet, DMB. The DMB is a pulled glass micropipette with a fine tip that contains a microscopic plug made of a hydrogel such as agar or polyacrylamide. This plug prevents flow but allows diffusive delivery of the molecule of interest from the DMB body into the cytosol, driven by its concentration gradient. This leads to a scheme of sustained intracellular dosing that is highly reproducible and quantifiable yet does not require the addition of solution volume to the cell. Potential loss of biomolecules from the cytosol through the plug of the DMB can be greatly reduced by proper choice of the pore size and tortuosity of the hydrogel in the DMB tip. The intracellular concentration of fluorescent molecules during delivery can be obtained calibration free. In this work we demonstrate dosing of Lucifer Yellow CH, LY, a charged fluorescent dye, into individual a7r5 vascular smooth muscle cells with a DMB. New types of quantitative analytical experiments on single live cells that the DMB technology enables are titration of intracellular ions and ligands, binding sites, and efflux pathways such as those that are involved in drug resistance.

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Year:  2008        PMID: 19551948      PMCID: PMC2771867          DOI: 10.1021/ac801670m

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  19 in total

1.  A galinstan expansion femtosyringe for microinjection of eukaryotic organelles and prokaryotes.

Authors:  M Knoblauch; J M Hibberd; J C Gray; A J van Bel
Journal:  Nat Biotechnol       Date:  1999-09       Impact factor: 54.908

2.  Fine chemical manipulations of microscopic liquid samples. 1. Droplet loading with chemicals.

Authors:  M Gratzl; H Lu; T Matsumoto; C Yi; G R Bright
Journal:  Anal Chem       Date:  1999-07-15       Impact factor: 6.986

3.  A direct comparison of whole cell patch and sharp electrodes by simultaneous recording from single spinal neurons in frog tadpoles.

Authors:  W-C Li; S R Soffe; Alan Roberts
Journal:  J Neurophysiol       Date:  2004-03-03       Impact factor: 2.714

4.  Optical detection in microscopic domains. 3. Confocal analysis of fluorescent amphiphilic molecules.

Authors:  Makoto Yoshida; Koji Tohda; Miklós Gratzl
Journal:  Anal Chem       Date:  2003-11-15       Impact factor: 6.986

5.  Quantification of gap junction selectivity.

Authors:  Jose F Ek-Vitorín; Janis M Burt
Journal:  Am J Physiol Cell Physiol       Date:  2005-08-10       Impact factor: 4.249

6.  Electrochemistry in microscopic domains. 1. The electrochemical cell and its voltammetric and amperometric response.

Authors:  R Kashyap; M Gratzl
Journal:  Anal Chem       Date:  1998-04-15       Impact factor: 6.986

7.  Complexometric determination of metal ions by microscopic diffusional titration.

Authors:  C Yi; D Huang; M Gratzl
Journal:  Anal Chem       Date:  1996-05-01       Impact factor: 6.986

8.  Gap junction communication mediates transforming growth factor-beta activation and endothelial-induced mural cell differentiation.

Authors:  Karen K Hirschi; Janis M Burt; Kendal D Hirschi; Cuiping Dai
Journal:  Circ Res       Date:  2003-08-14       Impact factor: 17.367

9.  Continuous in situ electrochemical monitoring of doxorubicin efflux from sensitive and drug-resistant cancer cells.

Authors:  C Yi; M Gratzl
Journal:  Biophys J       Date:  1998-11       Impact factor: 4.033

10.  A method for incorporating macromolecules into adherent cells.

Authors:  P L McNeil; R F Murphy; F Lanni; D L Taylor
Journal:  J Cell Biol       Date:  1984-04       Impact factor: 10.539

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