In last passage percolation models lying in the Kardar–Parisi–Zhang (KPZ) universality class, the energy of long energy-maximizing paths may be studied as a function of the paths’ pair of endpoint locations. Scaled coordinates may be introduced, so that these maximizing paths, or polymers, now cross unit distances with unit-order fluctuations, and have scaled energy, or weight, of unit order. In this article, we consider Brownian last passage percolation in these scaled coordinates. In the narrow wedge case, when one endpoint of such polymers is fixed, say at
, and the other is varied horizontally, over
, the polymer weight profile as a function of
is locally Brownian; indeed, by Hammond [‘Brownian regularity for the Airy line ensemble, and multi-polymer watermelons in Brownian last passage percolation’, Preprint (2016), arXiv:1609.02971, Theorem 2.11 and Proposition 2.5], the law of the profile is known to enjoy a very strong comparison to Brownian bridge on a given compact interval, with a Radon–Nikodym derivative in every
$p\in (1,\infty )$
, uniformly in the scaling parameter, provided that an affine adjustment is made to the weight profile before the comparison is made. In this article, we generalize this narrow wedge case and study polymer weight profiles begun from a very general initial condition. We prove that the profiles on a compact interval resemble Brownian bridge in a uniform sense: splitting the compact interval into a random but controlled number of patches, the profile in each patch after affine adjustment has a Radon–Nikodym derivative that lies in every
. This result is proved by harnessing an understanding of the uniform coalescence structure in the field of polymers developed in Hammond [‘Exponents governing the rarity of disjoint polymers in Brownian last passage percolation’, Preprint (2017a), arXiv:1709.04110] using techniques from Hammond (2016) and [‘Modulus of continuity of polymer weight profiles in Brownian last passage percolation’, Preprint (2017b), arXiv:1709.04115].