Verified locator: Biographical Memoirs77(1999), chapter Carl W. Gottschalk, opening p123: dates28April1922–15October1997 and byline MauriceB.Burg. Early research/micropuncture sections pp126–130: collaboration with Margaret Mylle, local fluid sampling, osmolality, dye/microdissection site verification. DOI10.17226/9681. Colleague-authored institutional memoir; original experimental observations separately cited to1959 paper.
Mark A. Knepper 2026-11-05
Mark A. Knepper is a researcher in kidney physiology who uses systems biology to investigate the regulation of water transport. A central example is how vasopressin changes the distribution of aquaporin-2 between the plasma membrane and the interior of collecting duct cells. His 2010 research report describes combining mass spectrometry, measurements of gene expression, mathematical modeling and physiological experiments to investigate this regulation.[ref]
The timing gives the mechanism its interest. On a scale of seconds to minutes, membrane trafficking can move existing aquaporin-2 into the plasma membrane, changing the route available for water movement. That is a different regulatory step from making additional aquaporin-2 through altered gene expression. Measuring how much channel protein exists and where it is located therefore answers different questions.[ref]
Mark A. Knepper also wrote a scientific remembrance of Maurice B. Burg, explaining how experiments on isolated renal tubules opened individual transport mechanisms to direct investigation.[ref]
Maurice B. Burg 2026-11-05
Maurice B. Burg was a researcher in renal physiology who developed experimental methods for studying individual nephron segments outside the intact kidney. Isolated tubule perfusion made it possible to relate transport properties to a particular anatomical segment, rather than observing only the final composition of urine.[ref]
The 1966 method paper by Maurice B. Burg and collaborators described preparations from single rabbit nephrons. Supplying fluid through an isolated renal tubule while controlling its surrounding solution allows the luminal and external conditions to be varied separately.[ref]
A useful experiment is to change the surrounding osmolality and compare entering and collected tubular fluid. A change in collected volume can reveal net water movement; changes in solute content address transport of dissolved substances. Isolating the segment constrains where the measured exchange occurred. The preparation simplifies the system while retaining an organized living epithelium, an important middle scale between a whole organ and an isolated protein.