<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Geng J</submitter><funding>NIGMS NIH HHS</funding><pagination>129-40</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2447896</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>182(1)</volume><pubmed_abstract>In yeast, approximately 31 autophagy-related (Atg) proteins have been identified. Most of them reside at the phagophore assembly site (PAS), although the function of the PAS mostly remains unclear. One reason for the latter is the lack of stoichiometric information regarding the Atg proteins at this site. We report the application of fluorescence microscopy to study the amount of Atg proteins at the PAS. We find that an increase in the amount of Atg11 at the PAS enhances the recruitment of Atg8 and Atg9 to this site and facilitates the formation of more cytoplasm-to-vacuole targeting vesicles. In response to autophagy induction, the amount of most Atg proteins remains unchanged at the PAS, whereas we see an enhanced recruitment of Atg8 and 9 at this site. During autophagy, the amount of At</pubmed_abstract><journal>The Journal of cell biology</journal><pubmed_title>Quantitative analysis of autophagy-related protein stoichiometry by fluorescence microscopy.</pubmed_title><pmcid>PMC2447896</pmcid><funding_grant_id>R01 GM053396</funding_grant_id><funding_grant_id>GM53396</funding_grant_id><pubmed_authors>Nair U</pubmed_authors><pubmed_authors>Klionsky DJ</pubmed_authors><pubmed_authors>Geng J</pubmed_authors><pubmed_authors>Baba M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quantitative analysis of autophagy-related protein stoichiometry by fluorescence microscopy.</name><description>In yeast, approximately 31 autophagy-related (Atg) proteins have been identified. Most of them reside at the phagophore assembly site (PAS), although the function of the PAS mostly remains unclear. One reason for the latter is the lack of stoichiometric information regarding the Atg proteins at this site. We report the application of fluorescence microscopy to study the amount of Atg proteins at the PAS. We find that an increase in the amount of Atg11 at the PAS enhances the recruitment of Atg8 and Atg9 to this site and facilitates the formation of more cytoplasm-to-vacuole targeting vesicles. In response to autophagy induction, the amount of most Atg proteins remains unchanged at the PAS, whereas we see an enhanced recruitment of Atg8 and 9 at this site. During autophagy, the amount of At</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Jul</publication><modification>2025-04-04T18:33:49.295Z</modification><creation>2019-03-27T00:15:46Z</creation></dates><accession>S-EPMC2447896</accession><cross_references><pubmed>18625846</pubmed><doi>10.1083/jcb.200711112</doi></cross_references></HashMap>