Atpase Activity

ATPase activity is the ability of an enzyme or protein complex to hydrolyze adenosine triphosphate (ATP), releasing energy that powers essential cellular work. During hydrolysis, ATP is converted to adenosine diphosphate (ADP) and inorganic phosphate, and the resulting energy drives conformational changes or chemical reactions in the protein. In biology, ATPases support membrane transport, muscle contraction, molecular motor activity, protein folding, and nucleic acid remodeling. Measuring ATPase activity helps researchers characterize enzyme function, evaluate regulation and inhibition, and understand how cells convert chemical energy into movement, transport, and other biological processes.

Atpase Activity - Related Videos

Research

JoVE Journal - Biology

Measuring In Vitro ATPase Activity for Enzymatic Characterization

0 Views •

Cited by 27 •

2016

We describe a basic protocol for quantitating in vitro ATPase activity. This protocol can be optimized based on the level of activity and requirements for a given purified ATPase.

Isolation of F1-ATPase from the Parasitic Protist Trypanosoma brucei

0 Views •

Cited by 1 •

2019

This protocol describes the purification of F1-ATPase from the cultured insect stage of Trypanosoma brucei. The procedure yields a highly pure, homogeneous, and active complex suitable for structural and enzymatic studies.

Chemical Modification of the Tryptophan Residue in a Recombinant Ca2+-ATPase N-domain for Studying Tryptophan-ANS FRET

0 Views •

2021

ANS binds to the Ca2+-ATPase recombinant N-domain. Fluorescence spectra display a FRET-like pattern upon excitation at a wavelength of 295 nm. NBS-mediated chemical modification of Trp quenches the fluorescence of the N-domain, which leads to the absence of energy transfer (FRET) between the Trp residue and ANS.

Purification of the Sarco-Endoplasmic Reticulum Ca2+-ATPase from Rabbit Muscle

0 Views •

2025

This protocol describes an improved SERCA purification method, which includes the disaccharide trehalose in the final centrifugation step. This carbohydrate stabilizes proteins under harsh conditions. The purified SERCA was catalytically active and displayed high purity, making it suitable for structural and functional studies.

Measuring Cation Transport by Na,K- and H,K-ATPase in Xenopus Oocytes by Atomic Absorption Spectrophotometry: An Alternative to Radioisotope Assays

0 Views •

Cited by 7 •

2013

We describe a method to quantify the activity of K+-countertransporting P-type ATPases by heterologous expression of the enzymes in Xenopus oocytes and measuring Rb+ or Li+ uptake into individual cells by atomic absorption spectrophotometry. The method is a sensitive and safe alternative to radioisotope flux experiments facilitating complex kinetic studies.

View All Results

FAQs

Related Topics